quadgram

This is a table of type quadgram and their frequencies. Use it to search & browse the list to learn more about your study carrel.

quadgram frequency
in the presence of124
nucleic acids res doi62
in the absence of58
human immunodeficiency virus type57
figure a and b55
and supplementary figure s50
severe acute respiratory syndrome47
supplementary figure s a45
on the other hand44
as shown in figure43
conflict of interest statement37
available at nar online36
the end of the35
figure b and c34
data are available at33
are available at nar33
supplementary data are available33
in the human genome32
supplementary figure s b32
in the case of32
in supplementary table s31
the human immunodeficiency virus29
in the context of29
at c for min28
at the end of27
the size of the26
the role of the26
can be used to26
surface of the protein24
was used as a23
the presence of a23
acute respiratory syndrome coronavirus22
as well as the22
as a function of22
of g s in22
shown in figure a22
the structure of the22
of the sukh superfamily21
of human immunodeficiency virus20
coronavirus ribosomal frameshifting signal19
has been shown to19
listed in supplementary table18
crystal structure of the18
the presence of the18
it is possible that17
at room temperature for17
supplementary figure s c17
in vitro and in17
of the stop codon17
a wide range of17
was added to the17
as a negative control17
in addition to the17
the base of the16
the context of the16
the length of the16
figure c and d16
figure e and f16
play a role in16
were carried out in15
one of the most15
exterior surface of the15
is consistent with the15
mutational analysis of the15
the exterior surface of15
the unfolded protein response15
have been shown to15
the position of the15
the importance of the14
is one of the14
lys mcm s uuu14
pay the open access14
is shown in figure14
presence or absence of14
the identity of the14
an important role in14
funding to pay the14
of a coronavirus ribosomal14
we were able to14
a large number of14
vitro and in vivo14
cells were transfected with14
trna lys mcm s14
fraction of fs m14
national center for biotechnology14
to pay the open14
shown in figure b14
the use of a14
the open access publication14
structure of the rna14
g s in the14
a u a u14
a final concentration of14
cells were treated with14
publication charges for this13
center for biotechnology information13
charges for this article13
of hepatitis c virus13
the majority of the13
for an rna pseudoknot13
access publication charges for13
open access publication charges13
of the s rrna13
used in this study13
c for min and13
the presence of template13
the terminal loop of12
the specificity of the12
cell leukemia virus type12
of the human immunodeficiency12
programmed ribosomal frameshifting in12
studies have shown that12
these data indicate that12
was carried out using12
was found to be12
component of a coronavirus12
this article was provided12
for min at c12
structure and function of12
a coronavirus ribosomal frameshifting12
correspondence should be addressed12
at the exterior surface12
whom correspondence should be12
the presence or absence12
the stability of the12
the hepatitis c virus12
article was provided by12
identification and characterization of12
in contrast to the12
the total number of12
it has been shown12
the surface of the12
in reading frame maintenance12
by the presence of12
to whom correspondence should12
the secondary structure of12
for this article was12
the virus variation resource12
supplementary figure s e11
to that of the11
in supplementary figure s11
at the base of11
were performed as described11
our results showed that11
the ability of the11
the presence of g11
the ese in exon11
for the detection of11
thermodynamic stability of the11
secondary structure of the11
incubated for min at11
been shown to be11
the fraction of fs11
of ribosomal frameshifting in11
coronavirus infectious bronchitis virus11
of the shift site11
the crystal structure of11
plays an important role11
mechanical explanation of rna10
state abundance of the10
c for s and10
the u a heptamer10
the presence of increasing10
ribosomal frameshifting in hiv10
in the vicinity of10
we would like to10
the national center for10
it is important to10
the severe acute respiratory10
rna pseudoknot function in10
that can be used10
of the viral genome10
majority of fs z10
the majority of fs10
bip and chop genes10
of severe acute respiratory10
performed as previously described10
of the homomorph is10
explanation of rna pseudoknot10
terminal segment of the10
used as a template10
crystal structure of a10
a mechanical explanation of10
is the number of10
the yeast saccharomyces cerevisiae10
of rna pseudoknot function10
base of the stem10
the presence of mm10
in programmed ribosomal frameshifting10
for h at c10
these results indicate that10
function in programmed ribosomal10
would like to thank10
for min at room10
min at room temperature10
pseudoknot function in programmed10
these results suggest that9
in the yeast saccharomyces9
performed as described previously9
nt downstream of the9
shown in figure d9
we have developed a9
the firefly luciferase gene9
has been shown that9
the ntd of dnag9
presence of g s9
expansion of decoding rules9
are shown in supplementary9
of the slippery sequence9
shown in supplementary table9
it is likely that9
table and supplementary figure9
on ice for min9
the fact that the9
interaction between madp and9
as described in the9
by the addition of9
in agreement with the9
variation in the human9
at c for s9
are listed in supplementary9
and function of the9
the location of the9
role of g s9
for the presence of9
this is consistent with9
we have shown that9
the thermodynamic stability of9
mutation of the ese9
stimulation of ribosomal frameshifting9
incubated at c for9
be used as a9
downstream of the slippery9
and supplementary table s9
destabilizing activity of vp8
we observed that the8
hepatitis c virus rna8
see also supplementary figure8
the sequences of the8
we found that the8
could be due to8
not included in the8
stop codon in the8
immediately downstream of the8
a part of the8
we conclude that the8
incubated for h at8
when compared to the8
as a result of8
for the development of8
was performed as described8
ribosomal pausing during translation8
these data suggest that8
the interaction between madp8
may be involved in8
have shown that the8
end of the genome8
are shown in figure8
these observations suggest that8
in exon of cd8
of an rna pseudoknot8
room temperature for min8
a limited number of8
of the frameshift site8
the s rrna transcript8
expression of sf asf8
on the basis of8
are listed in table8
the highly conserved residues8
figure s a and8
for human immunodeficiency virus8
of the uga codon8
appear to have been8
g s have been8
the vicinity of the8
alternative splicing of cd8
is responsible for the8
of the genetic code8
as a template for8
a u and a8
as well as a8
plays a role in8
also supplementary figure s8
at the surface of8
in the cytoplasm of8
figure c and supplementary8
moloney murine leukemia virus8
conservation at synonymous sites8
the nature of the8
it is possible to8
used as a negative8
room temperature for h8
the mcm side chain8
was observed in the8
in a number of8
in the a site8
the effect of the8
are likely to be8
previous studies have shown8
to determine whether the8
the ratio of the8
may play a role8
of the cyp d8
than that of the8
have been found in8
s a and s8
of decoding rules enriches8
the absence of the8
in the final assay8
the cyp d gene8
supplementary figure s d8
segment of the homomorph7
figure d and supplementary7
translation of an rna7
the interaction with the7
figure a and supplementary7
of the human genome7
quadruplex structures in the7
the number of methionines7
downstream of the frameshift7
translocational ribosome aligning with7
of the slippery site7
mechanisms by which coronaviruses7
see materials and methods7
at a frameshifter rna7
the expression of the7
of the ese in7
ensure synthesis of the7
to reading phase but7
pausing at a frameshifter7
which coronaviruses ensure synthesis7
in the synthesis of7
structural basis for the7
phase but shows little7
terminal edge of the7
supplementary table s and7
by which coronaviruses ensure7
the esterified methyl group7
of an efficient coronavirus7
solution structure of the7
substrate was annealed with7
for translational frameshifting in7
in the genome of7
in the regulation of7
we sought to determine7
achieving a golden mean7
synthesis of the correct7
for each of the7
frameshifter rna pseudoknot is7
the slippery site and7
in an elp mutant7
the hypothesis that the7
translational frameshifting in hiv7
stability of the first7
cells treated with mm7
little correlation with frameshift7
rules enriches gene expression7
ribosomal frameshifting in the7
reading phase but shows7
a subset of the7
pausing during translation of7
rna chaperone activity of7
has been reported to7
a frameshifter rna pseudoknot7
splicing pattern of cd7
of the effects of7
remains to be determined7
decoding rules enriches gene7
but shows little correlation7
is consistent with our7
of the sars coronavirus7
ratios of viral proteins7
the formation of the7
results showed that the7
structurally aligned sequences that7
region of the hiv7
correct stoichiometric ratios of7
bovine viral diarrhea virus7
efficient coronavirus ribosomal frameshifting7
of programmed ribosomal frameshifting7
stoichiometric ratios of viral7
have been identified in7
the pestivirus ns b7
and incubated at c7
the sequence of the7
it is known that7
to the reference genome7
c and supplementary figure7
to interact with the7
the vast majority of7
that the majority of7
requirement for an rna7
characterization of ribosomal frameshifting7
ge healthcare life sciences7
this suggests that the7
to the stop codon7
is possible that the7
is sensitive to reading7
coronaviruses ensure synthesis of7
rna pseudoknot is sensitive7
ribosomal pausing at a7
the rous sarcoma virus7
during translation of an7
of ribosomal frameshifting by7
the possibility that the7
the case of the7
the correct stoichiometric ratios7
edge of the motif7
of the correct stoichiometric7
trna arg mcm ucu7
for the prediction of7
is required for efficient7
the structurally aligned sequences7
binding of ncl to7
are consistent with the7
a member of the7
a function of time7
degradation of the s7
the t m of7
the activity of the7
middle east respiratory syndrome7
to the s rrna7
correlation with frameshift efficiency7
in the presence or7
in the expression of7
supplementary figure s and7
shows little correlation with7
be due to the7
shown in figure c7
and a u a7
the results of the7
the distance between the7
as well as in7
supplementary tables s and7
were used in the7
sensitive to reading phase7
an efficient coronavirus ribosomal7
tables s and s7
pseudoknot is sensitive to7
in the sample set6
in a viral rna6
luciferase reporter system for6
between mechanical strength of6
the occupancy status of6
in a j mice6
with respect to the6
is important to note6
of fs z is6
of the mcm side6
identification of a novel6
the number of sequences6
the c and c6
the ntd and the6
to a set of6
pseudoknots and ribosomal frameshifting6
is separated from the6
it has been reported6
movement impeded at a6
not affected by the6
between frameshift efficiency and6
pseudoknot enhance mechanical stability6
ifn induction by sh6
the viral g s6
at a pseudoknot required6
for frameshifting ribosomal pausing6
a wide variety of6
impeded at a pseudoknot6
was added to each6
can be found in6
of the u a6
characterization of an efficient6
stability and increase efficiency6
used to assess the6
a pseudoknot required for6
in each of the6
u and a u6
the formation of a6
stability and frameshift efficiency6
it should be noted6
a result of the6
a broad range of6
in support of this6
of the ebov trailer6
mrna pseudoknots promote efficient6
we propose that the6
d and supplementary figure6
position of the mutation6
stability of the stem6
was performed using the6
to verify that the6
the influence of the6
the slippery sequence and6
reporter system for studying6
required for frameshifting ribosomal6
the as rs interaction6
of the antisense strand6
correlation between mechanical strength6
that the presence of6
in the ltr promoter6
the first time that6
with the exception of6
b and supplementary figure6
expression of the full6
triplex structures in an6
mechanical stability and increase6
a final volume of6
and characterization of the6
is highly conserved in6
rna pseudoknots and ribosomal6
structure downstream of the6
in an rna pseudoknot6
time dlamp with hrm6
in tissue culture cells6
in the initiation of6
of the frameshift products6
s a and b6
that the structure of6
at the time of6
the tertiary structure of6
pseudoknots promote efficient programmed6
c bl j mice6
for the first time6
supplementary figures s a6
at the same time6
is essential for the6
reactions were incubated at6
to the reading frame6
of the template tunnel6
mechanical strength of messenger6
the efficiency of frameshifting6
the beginning of the6
transcript by the exosome6
a significant amount of6
u a slippery sequence6
tension on the mrna6
figure b and d6
buffer containing mm hepes6
of the de novo6
were carried out at6
of bip and chop6
glu mcm s uuc6
the copy number of6
assays were carried out6
and can be used6
the expression levels of6
that the ntd is6
enhance mechanical stability and6
buffer containing mm tris6
it was shown that6
and increase efficiency of6
in the mdx mouse6
viral replication and transcription6
should be noted that6
occupancy status of the6
of the hepatitis c6
one of the two6
under the following conditions6
immunodeficiency virus type rna6
how mrna pseudoknots promote6
is the mean of6
ie heptameric patterns clusters6
treatment with h o6
system for studying recoding6
with high t m6
for their ability to6
ribosomal frameshifting in decoding6
in buffer containing mm6
at c for h6
of the lacz gene6
rna pseudoknot enhance mechanical6
for studying recoding signals6
and analysis of the6
yeast ribosomal protein l6
the dynamic range of6
trna glu mcm s6
the structures of the6
of duchenne muscular dystrophy6
may be due to6
side of the hairpin6
pseudoknot required for frameshifting6
using a combination of6
the rna chaperone activity6
structures can act as6
the structural basis for6
carried out using a6
a critical role in6
trna gly mcm ucc6
probabilistic data structures and6
the levels of frameshifting6
the absence of a6
can be attributed to6
each end of the6
be observed in the6
the hj secondary structure6
frameshifting ribosomal pausing during6
lanes to in figure6
on the u a6
is important for the6
the composition of frameshift6
the results showed that6
role of sirt in6
strength of messenger rna6
has been reported that6
to a final concentration6
could be used to6
messenger rna pseudoknots and6
for the number of6
an rna pseudoknot enhance6
relative copy number of6
resuspended in lysis buffer6
and function of rna6
aligned sequences that comprise6
figures s a and6
the local stability of6
the function of the6
of messenger rna pseudoknots6
structures in an rna6
in an attempt to6
both in vitro and6
ribosomal movement impeded at6
of sf asf in6
the relative abundance of6
of the viral rna6
of the genome and6
under the control of6
consistent with the model6
new insights into the6
ribosomal frameshifting by antisense6
see supplementary table s6
in the kinetic model6
investigate the role of6
of and distance between5
both rna and dna5
was detected in the5
can also be used5
identification and analysis of5
slippery site and the5
did not have any5
figure a and c5
in the culture supernatant5
used as templates for5
in a dna sample5
the existence of a5
to the formation of5
a crucial initiator of5
type ii in vivo5
from a set of5
with mm h o5
the large ribosomal subunit5
unfolding of rna pseudoknots5
in the utr of5
pol ii occupancy at5
the interaction of sirt5
of the rna polymerase5
and were used for5
reported in the literature5
the coronavirus infectious bronchitis5
nucleotides downstream of the5
to trigger ifn activation5
figure and supplementary figure5
the abundance of the5
of increasing amounts of5
data suggest that the5
the evolution of the5
to the number of5
and distance between two5
database and analysis resource5
the maximum number of5
is consistent with a5
ribosomes stalled at the5
the relative expression of5
pseudoknot stem length in5
carried out in the5
leukemia virus type ii5
the degradation of the5
in materials and methods5
sequences of and distance5
the primer extension activity5
were cloned into the5
the role of rna5
as the size of5
gaba a receptor subunit5
it appears that the5
by the number of5
signals determine the efficiency5
the rate constant for5
final volume of ml5
the side of the5
east respiratory syndrome coronavirus5
of two or more5
this could be due5
ribosome aligning with dex5
the efficiency of ribosomal5
characterization of the frameshift5
helicase activity of the5
lower than that of5
supplementary figure s f5
codon in the spacer5
as the amount of5
interaction between pcaf and5
was performed as previously5
mixture was incubated for5
of the esterified methyl5
the efficiency of the5
and supplementary figures s5
the left of the5
be used to identify5
terminal part of sirt5
end of s rrna5
the sequences of and5
codon of the shift5
line probing analysis of5
the exterior of the5
in figure b and5
to test whether the5
the a u mutant5
mm nacl and mm5
to regulate gene expression5
by imbert et al5
initiator of ribosomal frameshifting5
the development of chemical5
in the fraction of5
esterified methyl group of5
can be used as5
for the interaction of5
we also observed a5
observed in the presence5
with the hypothesis that5
with the addition of5
treated with mm of5
the silencing activity of5
long terminal repeat promoter5
we note that the5
that the ntd of5
the conformation of the5
was provided by the5
in a similar manner5
of stop codon readthrough5
an important target for5
involved in the interaction5
by the exosome containing5
interaction of sirt with5
role of rna pseudoknot5
kindly provided by dr5
of the primers used5
by incubation on ice5
are summarized in figure5
of nucleic acids research5
atp and utp were5
the promotion of efficient5
in the frameshift site5
that there is a5
c in the presence5
to be present in5
signals in the mrna5
subgenomic mrna transcription in5
in the latter case5
in accordance with the5
of the role of5
the interaction between the5
error of the mean5
funding for open access5
exterior of the protein5
distance between two cis5
slippery sequence and the5
between the ntd and5
which is required for5
a role for the5
there was no significant5
domains a and a5
the catalytic domain of5
is similar to the5
stem length in the5
we have found that5
is illustrated in figure5
at a final concentration5
has been proposed to5
between the homomorphs of5
the cells were harvested5
of c for s5
our results suggest that5
pseudoknots involved in stimulating5
virus type and human5
as mrna destabilizing elements5
a role in the5
primers and were used5
hrm in the final5
at g for min5
length in the promotion5
the activity of nsp5
data structures and algorithms5
in this study are5
from pathway ii when5
rna pseudoknot stem length5
supplementary figures s and5
tomato bushy stunt virus5
conjugates d and d5
was not able to5
of the unfolded protein5
of the number of5
to induce ribosomal frameshifting5
a mouse model of5
in the cell nucleus5
ranging from to nt5
in the spacer region5
been identified in the5
binding affinity to the5
type and human t5
nt in length were5
e nucleic acids research5
are required for efficient5
of the firefly luciferase5
by the csl exosome5
located downstream of the5
can effectively substitute for5
c for min followed5
a relative copy number5
as well as by5
the model predicts that5
annealed with rna and5
the ntp entry tunnel5
of the mechanical unfolding5
of protein synthesis in5
from pathway iii when5
was annealed with rna5
between madp and ibv5
the wt and n5
tertiary structure of the5
figure b and supplementary5
at single nucleotide resolution5
pellet was resuspended in5
a new generation of5
is located at the5
can act as ribosomal5
directly adjacent to the5
cells were harvested h5
c for s for5
cycles of c for5
in supplementary tables s5
made it possible to5
renilla and firefly luciferase5
in the human immunodeficiency5
for the formation of5
in the target cells5
characterization of the mechanical5
development of chemical probes5
activation of the ifn5
was due to the5
standard error of the5
shown in figure e5
we show that the5
of ribosomal protein l5
in a variety of5
u mis and c5
aligning with dex xxy5
virus type ii in5
rna degradation by the5
the absence of theophylline5
determine the efficiency of5
true and false positives5
rna pseudoknots involved in5
as one of the5
of the mcm group5
promoter region of the5
classical swine fever virus5
of the cirv genome5
the uga stop codon5
important to note that5
standard rna helix substrate5
according to manufacturer instructions5
as a positive control5
twist on frameshifting pseudoknots5
were incubated at c5
in the bloom filter5
cells were infected with5
the mechanical unfolding of5
with the rdrp palm5
the interaction of the5
consistent with the hypothesis5
ese in exon of5
have been used to5
in the crystal structure5
an equal volume of5
terminal loop of helix5
act as ribosomal roadblocks5
comparable to that of5
institute of allergy and5
crucial initiator of ribosomal5
into the mechanism of5
over the past decade5
figure s and table5
the distribution of the5
of csfv ns b5
we find that the5
of rna pseudoknots involved5
this is the first5
and the ability to5
analysis of the rna5
responsible for the interaction5
kinase activity of cdk5
incubation on ice for5
a small number of5
lack of the mcm5
the past few years5
segment of the dpo5
multiple sequence alignment with5
the mrna entrance channel5
a u u a5
sequences of the primers5
of the mature s5
function of rna pseudoknots5
takes into account the5
section of figure a5
end of the homomorph5
in the recoding site5
was observed when the5
of the interaction between5
barr virus nuclear antigen5
in human immunodeficiency virus5
virus type rna dimerization5
of the large ribosomal5
figure e and supplementary5
the start of the5
sf asf expression vector5
stability and function of5
a potential target for5
in stimulating ribosomal frameshifting5
specific amplification in the5
from the beginning of5
were performed as previously5
the u a slippery5
in the promotion of5
both daudi and sk5
the gene of interest5
of rna pseudoknot stem5
diploid copy number of5
of the nucleocapsid protein5
similar to that of5
new twist on frameshifting5
motifs a and d5
activity of the ribosome5
be explained by the5
with rna and rna5
to the end of5
studies have demonstrated that5
exclude the possibility that5
not present in the5
of the sukh domain5
our data show that5
creb atf family proteins5
in the structure of5
d exd e motif5
the rest of the5
hydroxyl acylation analyzed by5
the viral life cycle5
was normalized to the5
mechanical unfolding of rna5
in a subset of5
involved in stimulating ribosomal5
by agarose gel electrophoresis5
s rrna transcript by5
of the wt and5
in dmem supplemented with5
of ribosomal frameshifting for5
to the ribosomal a5
followed by incubation on5
the presence of mg5
a new twist on5
rna secondary structure prediction5
and the number of5
in a mouse model5
ribosomal frameshifting in human5
to the cleavage site5
assays were performed as5
american type culture collection5
for a variety of5
copy number of the5
dimerization of human immunodeficiency5
the uaa stop codon5
the number of non5
for open access charge5
for min followed by5
performed as described earlier5
one of the three5
of the s group5
with the csl exosome5
the mixture was incubated5
was incubated for min5
the assumption that the5
efficiency of ribosomal frameshifting5
acting signals determine the5
a volume of ml4
the closing stem of4
for the mechanism of4
stopped by addition of4
of the third stem4
rna interference in mammalian4
by the fact that4
efficient in inducing frameshifting4
is based on the4
and mutagenic analysis of4
in the first step4
potential target for anti4
was kindly provided by4
in order to maintain4
ntd interacts with the4
contain at least one4
our data suggest that4
while the majority of4
bioinformatics database and analysis4
coupled transcription and translation4
t rnap and n4
the acvr b gene4
were incubated in the4
and analysis resource for4
frameshifting site is an4
and an important target4
small molecules that target4
sought to determine whether4
with fetal bovine serum4
deletion of the ese4
to bind to the4
the response of the4
false positives in the4
in the rous sarcoma4
role for g s4
confirmed by western blotting4
is composed of a4
used in the assays4
to test this hypothesis4
may contribute to the4
stability of base pairs4
each bar is the4
summarized in figure a4
in the u region4
the presence of theophylline4
the accuracy of the4
messenger rna during translation4
in decoding the sars4
two types of frameshift4
as the ratio of4
sequence determinant and an4
the amino acid sequence4
in bacteriophages and bacterial4
to the untranslated region4
was chosen as the4
was confirmed by western4
plus sf asf expression4
it is noteworthy that4
b and az c4
sequence database of genomes4
in agreement with previous4
when r t is4
of allergy and infectious4
and western blot analysis4
cells were harvested by4
that sf asf regulates4
trna gln mcm s4
g s in viruses4
of termination codons in4
have been reported in4
were obtained from the4
exogenous expression of the4
the members of the4
interacts with the exosome4
important target for antiviral4
of each of the4
a subset of these4
in the present study4
a version of the4
pseudoknot structures can act4
that is important for4
the homomorphs of motif4
in trna gln mcm4
the luciferase activity of4
both dna and rna4
it has been proposed4
translational recoding in the4
nucleotide and protein sequences4
flock house virus rna4
both specific and non4
using t rna polymerase4
reactions were terminated by4
regulatory protein sf asf4
as can be seen4
structures can effectively substitute4
the effects of the4
to see whether the4
sequences are listed in4
an in vivo dual4
protein database search programs4
in the wobble position4
the presence of mn4
the third stem of4
vascular endothelial growth factor4
the de novo initiation4
unwinding activity of vp4
end of the read4
total rna was isolated4
results indicate that a4
is close to the4
mapping cannot be found4
the rna recognition motif4
pro ribosomal frameshift signal4
in the previous section4
in gibbs free energy4
and evolution of the4
fs on the u4
alignment with high accuracy4
of the ncm group4
rx or rb repeats4
gln mcm s uug4
the large number of4
by gong and peersen4
to the use of4
of true and false4
show that the ntd4
the helix of the4
coli dnax ribosomal frameshifting4
were identified in the4
the mechanical strength of4
analysis of the stem4
pathosystems resource integration center4
emsa analysis of the4
of fs m was4
the presence of atp4
required for escherichia coli4
cov and s l4
overexpression of sf asf4
programmed ribosomal frameshifting the4
gene expression and replication4
were found to be4
the maximum rate of4
recoding in bacteriophages and4
rna binding activity of4
of a dna g4
were prepared as described4
were cloned into a4
coronavirus genes and genomes4
a greater number of4
dnag is important for4
part of the stem4
control of gene expression4
to be important for4
the component of the4
the frameshift stimulatory signal4
is known about the4
database of experimentally validated4
by in vitro transcription4
the ribosome is paused4
secondary structure prediction and4
see material and methods4
the shift site and4
prf activity of switch4
critical reading of the4
the protein data bank4
affected by the elp4
were added to the4
referred to as the4
frameshifting triplex structures in4
frameshifting by antisense oligonucleotides4
lysate was incubated with4
denaturation at c for4
the number of true4
of the est mrna4
of specific and non4
leukemia virus type i4
involved in rna metabolism4
is due to the4
a dual fluorescence reporter4
and the position of4
of a j mice4
that sirt interacts with4
b and b c4
the relative expression levels4
role of the downstream4
local stability of the4
differential melting curve analysis4
de competent cells and4
frequent presence of an4
using t polynucleotide kinase4
and trna glu mcm4
carried out at room4
purchased from new england4
figure k and l4
subunit of dna polymerase4
of the infected cells4
can be used for4
as shown in figures4
involved in ribosomal frameshifting4
amount of fs m4
it would be interesting4
with a nt asymmetric4
with high accuracy and4
and functional analysis of4
in the formation of4
site trna is a4
tested the ability of4
primer extension activity of4
the active site closure4
templates for in vitro4
with the number of4
the utr of the4
of sirna and silna4
the downstream firefly luciferase4
acting rna signals for4
in the terminal loop4
amplification in the presence4
compared to the other4
decrease in frameshift efficiency4
dna polymerase iii holoenzyme4
virus type ribosomal frameshifting4
guide strand from the4
of protein database search4
value for each bar4
rna signals for translational4
the long terminal repeat4
resulted in a reduction4
both nsp and nsp4
is not restricted to4
as a potential target4
in the form of4
experiments were carried out4
acts as a linchpin4
active mechanisms to unwind4
figure d and e4
adjacent to the uga4
frameshifting during translation of4
s and c for4
with increasing concentrations of4
the degree of conservation4
of the large subunit4
sequence upstream of the4
on the same genomes4
freely available at http4
the rt stop codon4
frameshifting in decoding the4
the uga codon of4
in pol ii transcription4
that is complementary to4
a significant decrease in4
gamma subunit of dna4
are presented in figure4
the first base of4
is composed of an4
only a subset of4
is known to be4
internal ribosome entry site4
base following the stop4
trna is a crucial4
to the fact that4
gapped blast and psi4
at the national center4
relative to that of4
is thought to be4
assay was performed as4
treatment of duchenne muscular4
high accuracy and high4
available online at http4
in histone h b4
mutagenic analysis of the4
and the role of4
accuracy and high throughput4
with the observation that4
in the number of4
generation of protein database4
the base following the4
ribosome aligning with xxy4
was used as the4
we find that positional4
in the input set4
added to the reaction4
at the level of4
an invariant sequence determinant4
interference in mammalian cells4
proteins were eluted with4
mrna destabilizing elements through4
activities of the wt4
levels of frameshifting are4
to the sukh superfamily4
that the ability of4
efficient stimulation of site4
the integrity of the4
b cell line daudi4
that the l p4
the innate immune response4
the wobble position of4
through the use of4
as the only ntp4
nucleotide sequence of the4
novel application of srna4
ns b and the4
are given in table4
shown that sirt is4
a complete loss of4
of fs m is4
was carried out in4
gels were dried and4
az b and az4
immunodeficiency virus type ribosomal4
also been shown to4
luciferase assay system for4
is required for the4
this work was supported4
binding site for a4
a high level of4
the second type of4
with the ese site4
in coronavirus rna synthesis4
type ribosomal frameshifting site4
to a lesser extent4
of the pip a4
with severe acute respiratory4
version of this article4
the number of false4
z and fs m4
it was noted that4
in comparison to the4
possible explanation for this4
the target gene and4
nuclease toxins of the4
would lead to a4
has been implicated in4
is an invariant sequence4
is also supported by4
translational frameshifting in the4
for each bar is4
the frequency of frameshifting4
a new read segment4
of rna polymerase ii4
of pcaf in the4
confirmed by dna sequencing4
assay system for studying4
to better understand the4
and exogenous expression of4
results suggest that the4
mcm s uuu and4
referred to as n4
a heptamer supports a4
fold higher than the4
study of the effects4
the number of unique4
accepted to the a4
formed by domains a4
length dependence of programmed4
with standard error of4
the role of g4
to in figure a4
pseudoknot is required for4
specific ribosome frameshifting by4
escherichia coli dnax ribosomal4
interaction with the exosome4
in the first place4
be found in the4
prf occurs during translocation4
bacteriophages and bacterial is4
in the viral life4
level of exon skipping4
ribosomal frameshift in the4
ribosomal frameshifting triplex structures4
for studying translational recoding4
hek t cells were4
it has been hypothesized4
of gaba a receptor4
position of x residues4
ii iii iv and4
the only ntp substrates4
invariant sequence determinant and4
studying translational recoding in4
d exd e motifs4
a and supplementary figure4
the mdx mouse model4
intensity of fs product4
in a manner that4
of chemical probes for4
on the same genome4
our result showed that4
using a cocktail of4
binding mutant k a4
proteolytic processing in the4
of the in vitro4
ribosomal frameshift signal in4
is defined as the4
the west nile virus4
on the amount of4
is a crucial initiator4
can be explained by4
the ncbi virus variation4
the translation elongation cycle4
as a proof of4
with the hhpred program4
programmed ribosomal frameshifting by4
similar results were obtained4
of the rna pseudoknot4
the synthesis of the4
sequences based on standardized4
fs product intensity of4
end of the mrna4
nt upstream of the4
b b and b4
mouse hepatitis virus rna4
mechanisms to unwind messenger4
fs z and fs4
was replaced by a4
the csl exosome and4
a d and i4
cell growth and proliferation4
used to identify the4
were also used to4
analyzed by primer extension4
the kinase activity of4
figure f and supplementary4
a receptor subunit genes4
the ncbi taxonomy database4
probabilistic and signal processing4
the mrna in the4
in the production of4
sequences listed in supplementary4
new generation of protein4
is present in the4
of increasing concentrations of4
of dna polymerase iii4
of the sense strand4
the first base pair4
by western blot analysis4
between the slippery site4
activity of the g4
the removal of the4
were resolved by sds4
be involved in the4
samples were separated on4
significant levels of frameshifting4
expression levels of the4
in figure a and4
heterogeneous nuclear ribonucleoprotein a4
were grown in sc4
a function of the4
the primers used for4
rrna transcript by the4
able to interact with4
consistent with our previous4
and is consistent with4
to the shift site4
of rna polymerase i4
gov genome viruses variation4
to the unmodified sirna4
of the cleavage site4
like to thank dr4
to include more viruses4
between in vitro and4
represented by r t4
these results demonstrate that4
reading frame relative to4
is supported by the4
of two types of4
a lack of correlation4
cells were seeded in4
has been suggested to4
the lack of a4
total rna was extracted4
linked to the sukh4
of the moloney murine4
competent cells and grown4
for escherichia coli dnax4
reading frame of the4
of s rrna and4
can be seen in4
extension activity of nsp4
ncbi virus variation resource4
international nucleotide sequence database4
inhibitory activity of the4
the possible role of4
to unwind messenger rna4
and incubated for h4
copy number of a4
c c of the4
and bacterial is elements4
ribosomal frameshifting characterization of4
the predicted cleavage site4
a correlation between the4
selective amplification of the4
system for studying translational4
the comparative rna web4
for the interaction with4
luciferase bicistronic reporter system4
consistent with previous studies4
the role of sirt4
at the frameshift site4
on the ribosome are4
and incubated for min4
sirt is associated with4
the promoter region of4
did not change the4
frameshifting in human immunodeficiency4
presence of increasing amounts4
presence of increasing concentrations4
was observed with the4
resolution structure of the4
signals for translational frameshifting4
of the x xx4
recoding in the yeast4
as part of the4
tested the effect of4
a component of the4
as described in supplementary4
firefly luciferase bicistronic reporter4
pea enation mosaic virus4
renilla firefly luciferase bicistronic4
uses two active mechanisms4
on the surface of4
the native s rrna4
the wt ns b4
computational tools for the4
on the slippery sequence4
by the viral rdrp4
ntd and the rdrp4
ribosome uses two active4
ns x denotes the4
figure and supplementary data4
amount of frameshifted ribosomes4
the production of two4
frame codons in the4
rna was extracted from4
a splicing regulatory protein4
the csfv ns b4
the part of the4
values were determined by4
the specific binding of4
the average of the4
two active mechanisms to4
the structure of motif4
in a volume of4
frameshifting characterization of the4
the interaction between pcaf4
were translated in rrl4
as a means to4
in the s rrna4
by one of the4
that the expression of4
transcription and translation reactions4
dependent rna polymerase and4
of a ribosomal frameshifting4
abundance of the est4
cells were grown overnight4
we also show that4
mrna helicase activity of4
the digital array is4
that most of the4
over a wide range4
when atp and utp4
by sox in cells4
analysis at single nucleotide4
of the ntd and4
effect by modification deficiency4
length and truncated cd4
of antisense morpholino oligomers4
then used as the4
bar is the mean4
step at c for4
w c p s4
frameshifting by antisense lna4
unwind messenger rna during4
the same as the4
the mrna and the4
in lithium cacodylate buffer4
from new england biolabs4
interacts with the rdrp4
the entrance of the4
been found in the4
are located in the4
acylation analyzed by primer4
in the elution fraction4
between wild type and4
in the central region4
these results show that4
terminal d exd e4
dependent rna polymerase from4
the a u a4
for the discovery of4
determinant and an important4
cognate or near cognate4
redundant sequence database of4
the alternative splicing pattern4
the use of g4
these data support the4
was referred to as4
for each set of4
the presence of mbp4
the rate of a4
indicates that the structure4
in the supplementary materials4
is not affected by4
the international nucleotide sequence4
independent experiments with standard4
in a wild type4
the moloney murine leukemia4
were not present in4
of the rna complex4
reactions were carried out4
resulted in a significant4
in the nef coding4
rna structure analysis at4
for the binding to4
has been proposed that4
of the ternary complex4
the s ribosomal subunit4
r t is s4
the mechanism by which4
min at c and4
out at room temperature4
change in gibbs free4
to be able to4
of bovine viral diarrhea4
for in vitro transcription4
rna polymerase structural basis4
splicing regulatory protein sf4
mutational analysis of cis4
neuronal cell line sk4
in coding regions of4
u mis assays were4
in the reading frame4
of viral g s4
been shown to stimulate4
the s and s4
each of the three4
national institute of allergy4
a portion of the4
the amount of frameshifted4
all constructs were verified4
in most of the4
is predicted to be4
aligning with xxy yyz4
of the rna structure4
stimulation of stop codon4
the same sequence as4
frameshifting on a u4
s target genes in4
of flock house virus4
the mcm group of4
reading of the manuscript4
that there is no4
it is believed that4
binding to the exosome4
following the stop codon4
e and supplementary figure4
have a role in4
structure of the eukaryotic4
the homomorphs of motifs4
the rna binding activity4
that the vast majority4
in the second step4
s and s ribosomal4
at the slippery site4
the p luc vector4
are in agreement with4
ribosomal frameshifting on a4
with the end of4
assays were performed with4
was shown to be4
ribosome frameshifting by antisense4
structure of the hiv4
crystal structures of the4
the structure and function4
gene and protein annotation4
ucc uga shift site4
to determine whether this4
the molecular biology of4
the main body of4
see supplementary table online4
cells and grown in4
was carried out at4
heptamer supports a role4
of mutations in the4
x denotes the orfs4
structural probing and mutagenic4
of trna lys mcm4
yeast saccharomyces cerevisiae the4
composition of frameshift products4
through the nmd pathway4
comparative mutational analysis of4
and in the presence4
mrna pseudoknot structures can4
in light of the4
proteins involved in rna4
the b b and4
k ay a mutant4
in the course of4
taq and t dnap4
the gamma subunit of4
through the interaction with4
avian infectious bronchitis virus4
the untranslated region of4
results are consistent with4
essential for the interaction4
sequence alignment with high4
after mutation of the4
involvement of pcaf in4
in both daudi and4
the role of this4
structure analysis at single4
terminus of pip a4
for s and c4
loop required for escherichia4
important for human immunodeficiency4
an increase in fs4
in binding of rna4
figures a and a4
be noted that the4
cells were maintained in4
level of sf asf4
the progression of the4
k ay a was4
transcriptional quality control of4
ribosomal frameshifting site is4
barley yellow dwarf virus4
find that positional clustering4
in bacteria and archaea4
to determine whether vp4
the ribosome uses two4
of the cpv capsid4
cell death in yeast4
immunodeficiency virus type and4
target for antiviral therapy4
rosetta de competent cells4
to play a role4
a component of a4
experiments with standard error4
in the elp mutant4
that sirt is associated4
a nt asymmetric bulge4
the number of nucleotides4
were harvested by centrifugation4
site is an invariant4
we found that a4
the wall of the4
at different time points4
s and table s4
presence of an extended4
site of the ribosome4
there appears to be4
trna pro ncm ugg4
r t and r4
of the second pmo4
supports a role for4
as well as other4
this is an open4
the observation that the4
probing and mutagenic analysis4
main body of zbd4
has been hypothesized that4
singly conjugated pip a4
frameshifting on viral rnas3
of ribosomal pausing during3
in the protein data3
slippery site composition on3
are separated by a3
how to make sense3
polyadenylation of the s3
the length of each3
is derived from the3
we suggest that the3
translocation to the p3
at a frequency higher3
h d class ii3
hepatitis c virus infection3
were grown overnight in3
at a significant level3
of coronavirus infectious bronchitis3
of the s and3
by centrifugation at r3
the top of the3
for the production of3
polyprotein encoded by orf3
decoding in cellular gene3
frameshift in the human3
were made on the3
of the digital array3
and proteolytic processing in3
the original work is3
is involved in the3
readthrough of a uga3
insertion and substitution events3
position of the anticodon3
involved in viral programmed3
appears to be a3
of the mrna and3
to mg ml and3
is based on a3
sequences have been identified3
site for a splicing3
gene by ribosomal frameshifting3
model has been proposed3
transcripts by the exosome3
completed with a final3
frameshift efficiency and the3
of sox bound to3
was analyzed as described3
motif c precedes motif3
examples of frameshifter hairpins3
in a single transcript3
from a single polycistronic3
attenuation structure for sg3
as a consequence of3
role of the rna3
nt of the uga3
distributed under the terms3
it is plausible that3
it will be interesting3
q and y f3
are one of the3
structure of the ebov3
of recombination events in3
unique cluster of g3
with two tm segments3
the root of the3
determined by taking the3
in cultured mammalian cells3
two macrodomains that bind3
function analysis of the3
interactions in plant virus3
dmd and acvr b3
and firefly luciferase genes3
the ability of this3
the stop codon in3
figures c and d3
rrna by the exosome3
studies have focused on3
incomplete translocation in pathway3
for yeast m double3
which are likely to3
present in each product3
agg cca ggg aat3
conserved features of genome3
has been studied extensively3
associated with severe acute3
by their ability to3
the role of wobble3
different groups of coronaviruses3
products analysed and quantified3
a frequency higher than3
reading the slippery codon3
is available at nar3
at the entrance of3
were purchased from sigma3
is independent of the3
by the archaeal exosome3
extension at c for3
on taxonomy of viruses3
the involvement of pcaf3
the stop codon on3
the presence of both3
the most frequently recurring3
were used as templates3
sarcoma virus pol gene3
of herpes simplex virus3
peptides experimentally tested for3
tcc tac aag gga3
to the ntc or3
washed with ml of3
k ay a protein3
be used as an3
a template for the3
a stop codon in3
of the target gene3
proteins encoded by orfs3
calculated by dividing the3
the genome sequence of3
to a single cpp3
base pairs in the3
the most efficient motifs3
investigated in a wild3
in the supplementary data3
and mechanism a mechanical3
in the p site3
is induced by a3
and the antisense primer3
reduction between and of3
involved in the regulation3
addition of serum to3
of a recombination junction3
frameshifting are frequent in3
the sukh superfamily gene3
ttt tta ggg aag3
be used to reduce3
site trna ggg pro3
downstream of the motif3
data are consistent with3
component of a larger3
to premature termination codons3
ctt gga taa ag3
the digital pcr analysis3
of the barley yellow3
and compared to the3
the wt and mutant3
by imagequant tl software3
with a mixture of3
rna was extracted with3
at the first position3
ltr g complex bands3
we demonstrated that the3
phosphorylated ends of rna3
proper reading frame maintenance3
interaction essential for efficient3
heptanucleotide sequence x xxy3
expression of cd in3
sequence identity of the3
the structure and dynamics3
a mismatch is found3
ribosomal frameshifting in coronavirus3
and c bl j3
group of the mcm3
a reduction between and3
a uga stop codon3
ribosomal frameshifting for human3
of a series of3
is the value of3
as well as for3
in the polyprotein encoded3
or rtsl rna samples3
the prediction of peptides3
of the protein in3
physicochemical properties and predicted3
wt ns b and3
in the toprim domain3
play a critical role3
nucleic acid folding and3
from two independent experiments3
products of human t3
sequences in saccharomyces cerevisiae3
dependent activation of the3
remains identical to the3
quadruplexes in the human3
genome and proteome of3
destabilizing elements through at3
its entirety but only3
the central region of3
structure of the pseudoknot3
h o and menadione3
that the specific binding3
of a small molecule3
presence of mbp alone3
and quantified by imagequant3
media supplemented with kanamycin3
part or as a3
were determined by a3
identification of a new3
and end of the3
a significant fraction of3
schematic representation of the3
out as previously described3
binds to the ese3
number of recombination events3
the hcv ns b3
western blot analysis with3
were separated on a3
least two molecular pathways3
under the terms of3
ltr promoter activity was3
wobble uridine modifications in3
a single copy gene3
derive from ribosomal frameshifting3
base pairs at the3
terminal domain of the3
proteins have been identified3
a j and c3
ncbi viral genomes resource3
analysis of bicistronic reporter3
as well as with3
grown for h at3
positions with real mutations3
the alternative splicing construct3
by the wellcome trust3
effects of heptameric slippery3
of sars coronavirus contains3
page for retrieval of3
and merged bloom filter3
a complete set of3
the relationship between the3
compared to the wild3
using the blastclust program3
aag atc tgg cct3
is encoded by the3
sars coronavirus genome expression3
and the requirement of3
data support the notion3
to daudi or sk3
codon at a time3
results indicate that the3
three transfer rnas occupying3
of comparative sequence and3
pathway ii when r3
end of the oligonucleotide3
ability of the sukh3
the mechanism of frameshifting3
efficiency was calculated by3
cell lysates prepared from3
rnas derived from nco3
the regulation of the3
that a downstream pseudoknot3
the affinity of the3
immunodeficiency virus type particle3
specificity of the interaction3
u containing trna gly3
prediction of peptides binding3
is crucial for the3
mm mn was supplemented3
destabilizes rna helices and3
were separated by sds3
the intensity of the3
our in vitro assay3
did not result in3
first base of the3
as an anchor for3
may arise from a3
shift site and the3
in which the first3
signal beginning at nucleotide3
in the analysis of3
set of rna samples3
increase in fs exp3
of sf asf increased3
as the number of3
of sf asf was3
using the primers listed3
the modified wobble nucleoside3
in both bacteria and3
a pt in the3
unable to form the3
containing trna gly mcm3
pluc cells were treated3
we decided to use3
ii iii iv g3
two molecular pathways in3
from ft cells transfected3
significant fraction of the3
in vitro transcribed s3
the p and a3
a common feature of3
beet western yellows virus3
the core of the3
structure of the nsp3
the genome of saccharomyces3
compared to wild type3
of rna secondary structure3
effectively substitute for an3
between the end of3
repeated at least three3
the binding to the3
cca ggg aat ttt3
for rna quality assessment3
of the frameshift motif3
structure of a ribosomal3
west nile and japanese3
blot analysis of the3
importance of ribosomal frameshifting3
this study was to3
beet western yellows luteovirus3
of the rous sarcoma3
for min and the3
step in the synthesis3
secondary structure in the3
cells were cultured in3
for rapid mutation scanning3
genome sequence of the3
of the conserved heptameric3
number of probes required3
a highly structured rna3
expression of two isoforms3
methyl group of the3
is stimulated by a3
the rate of translation3
were no significant differences3
site effect by modification3
sequences that direct significant3
a possible explanation for3
and utp were supplied3
the ntd is a3
at the position of3
uptake by the target3
cdk and cyclin t3
mechanisms and enzymes involved3
hepatitis c virus internal3
nucleotide sequence database collaboration3
the ntd and ctd3
bloom filter for the3
table and supplementary table3
rna binding by epstein3
as well as to3
integrate results from multiple3
and then treated with3
structure information for ribosomal3
in sequence and structure3
original work is properly3
was determined to be3
as the search model3
by the amount of3
molecular pathways in yeast3
which permits unrestricted non3
as a derivative work3
copolymerization of pyrrole and3
the catalytic subunit of3
in the escherichia coli3
have been described earlier3
end of the sense3
as a linchpin that3
of the homomorph and3
of sequences based on3
occurs on the phosphate3
a slight increase in3
directly involved in the3
to be encoded by3
the center of the3
of the hairpin stem3
able to distinguish the3
in the translation of3
a direct role in3
the u region of3
the ribosome characterization of3
dna replication and metaphase3
able to trigger ifn3
d r t is3
clinically relevant concentrations of3
in siv is induced3
interactions between the ntd3
annotation of recoded genes3
access article distributed under3
to the reference sample3
rous sarcoma virus gag3
was not present in3
the mouse hepatitis virus3
differentiate specific and non3
mechanism a mechanical explanation3
of this domain in3
be interesting to see3
the rna signal essential3
is supported by a3
highly structured rna stem3
in the zero frame3
from the sk snrnp3
a possible role in3
the frameshift signal of3
tension in the mrna3
y can be a3
may provide insight into3
direct evidence for a3
suppresses the innate immune3
of frameshifting are frequent3
to investigate the role3
a vital role in3
structure and mechanism a3
and may also be3
between the slippery sequence3
that the specificity of3
error rate of virema3
helicases and nucleic acid3
translational termination efficiency in3
by the degradometer software3
cells transfected with the3
h d class i3
which correspond to the3
of mouse hepatitis virus3
conjugation of the second3
by the rotavirus classification3
crystal structure of sox3
is referred to as3
induced by a highly3
rotavirus classification working group3
at the expense of3
northern blot signal intensity3
cyclin t from the3
analysis was performed on3
the stronger the pseudoknot3
the northern blot signal3
of the ring module3
frameshifting among different eukaryotic3
rna pseudoknot component of3
of the rna signal3
of the location of3
of heptameric slippery site3
number of occurrences of3
from an h promoter3
of the nature of3
in t rna polymerase3
cell and in vivo3
signals for ribosomal frameshifting3
site and the beginning3
firefly and renilla luciferase3
the coronavirus group lineage3
shift in reading frame3
the tree of life3
reading frame due to3
for min in the3
incidence of false positives3
across the randomized nrmegs3
and quantified using a3
that it might be3
a viral rna pseudoknot3
the ctd of dnag3
function as mrna destabilizing3
pcr reactions were performed3
to exclude the possibility3
grown to early exponential3
is completely conserved in3
from the slippery site3
as suggested by the3
absence of the s3
the rna secondary structure3
in a trm mutant3
the stop codon and3
at the top of3
between pcaf and xbp3
the positive predictive value3
are characterized by a3
role of wobble uridine3
results from multiple sampling3
number of the gene3
sequences have been found3
the mcm s u3
in the most conserved3
is likely to have3
a role for g3
was measured using a3
alignment and tree building3
by rna polymerase ii3
s and s rrna3
end of the pip3
the ncbi influenza virus3
subtilis detection capture probe3
virus internal ribosome entry3
site effect caused by3
recent crystal structure of3
is part of the3
is not included in3
of the nuclease domain3
creative commons attribution non3
base of the motif3
or between experimental runs3
that were used as3
using a typhoon variable3
ribosomal pausing during programmed3
messenger rnas derived from3
of the codon context3
structural basis for proteolysis3
the amount of protein3
which is known to3
use a combination of3
stained with ethidium bromide3
extraction and ethanol precipitation3
with fetal calf serum3
that of the wt3
signal with the ribosome3
of group a coronaviruses3
ribosome are involved in3
subsequently reproduced or disseminated3
the absence of added3
sensitivity and error rate3
the ese site deleted3
of the frameshift signal3
in the relative expression3
a combinatorial rnai approach3
efficiency measured for each3
systematic analysis of bicistronic3
bacterial insertion sequence is3
of the rease fold3
pol ii phosphorylated at3
uga codon of the3
been deposited in the3
into the final assay3
in the past few3
a comprehensive analysis of3
in the mrna and3
strength of a pseudoknot3
by antonov et al3
s and s rrnas3
the renilla and firefly3
exposed to a phosphorimager3
ns b and its3
a and p sites3
because they are not3
activation of the poliovirus3
described in supplementary figure3
among different eukaryotic systems3
at the wall of3
in viral replication and3
the illumina miseq platform3
nmr structure of the3
number of leading zeros3
is also involved in3
quadruplex rna binding by3
of viral rna genomes3
antigen in dna replication3
due to the use3
sufficient to trigger ifn3
this observation is that3
and reproduction in any3
total rna extracted from3
are known to be3
downstream mrna secondary structure3
transformation of intact yeast3
and error rate of3
heptameric slippery site composition3
stem of the sars3
ay a protein was3
od and grown overnight3
virus gene expression and3
a wild type and3
region regulates the hiv3
mechanism to integrate results3
the stalling of the3
the sensitivity and error3
were subjected to a3
the sukh superfamily that3
a u a heptamer3
b expressed from an3
is located near the3
were used as positive3
pluc cells were seeded3
in veev and sinv3
we hypothesize that the3
in rrl and products3
and e sites on3
sars coronavirus contains two3
comes from pathway iii3
result is consistent with3
variability at synonymous sites3
below the relevant lanes3
and the fitness of3
of the amino acid3
determine the level of3
in a significant decrease3
sequence was changed to3
frameshifting is stimulated by3
to in figure c3
the slippery codon ggg3
of the motif is3
it was suggested that3
u a heptamer supports3
at least in vitro3
products were analyzed using3
of the pseudoknot to3
ribosomes to premature termination3
in its entirety but3
the beads were washed3
cysteines of the treble3
a derivative work this3
mutation or deletion of3
of methionines present in3
the background of the3
revealed that the ntd3
of cdk cyclin t3
systems such as the3
clinical sensitivity and specificity3
the renilla firefly luciferase3
cells were seeded h3
quantified by imagequant tl3
in the family reoviridae3
interesting to note that3
for nmr studies of3
the ucc uga shift3
formation of a unique3
structure of motif c3
enhanced synonymous site conservation3
significantly higher levels of3
in upf d cells3
of the human cd3
a role for messenger3
were calculated for each3
to trigger ifn induction3
a linear relationship between3
posttranscriptional quality control of3
the structure of a3
were used for each3
identical to the ntc3
database of comparative sequence3
beet necrotic yellow vein3
the ncm group in3
acid folding and hybridization3
biotinylated thymidine in the3
to activate ifn production3
in out of the3
can be observed in3
number of unique k3
the beginning of a3
and g w mutant3
digital pcr analysis software3
in the input sets3
illustrated in figure b3
be caused by the3
u containing trna pro3
volume of ml in3
time pcr reaction was3
server for nucleic acid3
is important for human3
reproduction in any medium3
of the archaeal exosome3
the s rrna degradation3
a slow entry of3
reading frame maintenance is3
an rna pseudoknot loop3
vp in the standard3
from hek t cells3
increased expression of sf3
pelleted by centrifugation at3
were not able to3
encountered by the ribosome3
the serum concentration increased3
ribosomal frameshifting solution structure3
to the lack of3
the use of different3
replaced by an rna3
a small set of3
acids secondary structures that3
the balb c mouse3
the expression of xbp3
bands were quantified using3
a heptanucleotide slippery sequence3
from c to c3
the rna pseudoknot component3
hrm is not incorporated3
a t m of3
on bip and chop3
of rna by parp3
used as a control3
human b cell lines3
pcr and quantitative chip3
at room temperature in3
we show that in3
have revealed that the3
of s rrna by3
pk and theophylline aptamer3
the transfected cells and3
is likely due to3
a linchpin that stabilizes3
that antisense oligonucleotides can3
translational accuracy and the3
figures a and b3
rna polymerase structure of3
was performed using a3
insights into the mechanism3
of the toprim domain3
genomes and their genes3
of cp l template3
proximal to the quencher3
a central role in3
absence of a control3
for comparative genome analysis3
s ribosomal rna bands3
from the coronavirus group3
association of sirt with3
ncm u containing trna3
was transformed into rosetta3
d r t and3
is indicated below the3
rna in caenorhabditis elegans3
the observation in the3
particle assembly and replication3
final extension step at3
an alternative reading frame3
were grown for h3
instead of a cognate3
encephalitis flaviviruses suggests ns3
e ldr and acde3
using the same primers3
amino acid sequence of3
expression of the rous3
ribosomal frameshifting efficiency and3
through the addition of3
the relative amount of3
interactions with the rdrp3
pt in the kinetic3
of the trnas in3
pol gene products of3
use of g ligands3
is a prerequisite for3
of annotated coronavirus genes3
due to the fact3
of the arterivirus helicase3
by the target cell3
the two components of3
as the serum concentration3
encoded by orf ab3
heater and temperature sensor3
for the treatment of3
whether the presence of3
of the bacterial ribosome3
and specific genetic interference3
a role in regulating3
knockdown of sf asf3
higher level of misincorporation3
type rna dimerization and3
with the formation of3
article is subsequently reproduced3
in combination with a3
are amino acids long3
online database of comparative3
form a new segment3
article distributed under the3
essential for translational frameshifting3
the and ends of3
distinguished from the wild3