key: cord-0799500-93ldjyi5
authors: Chen, Yan; Li, Xue; Su, Liyao; Chen, Xu; Zhang, Shuting; Xu, Xiaoping; Zhang, Zihao; Chen, Yukun; XuHan, Xu; Lin, Yuling; Lai, Zhongxiong
title: Genome-wide identification and characterization of long non-coding RNAs involved in the early somatic embryogenesis in Dimocarpus longan Lour
date: 2018-11-06
journal: BMC Genomics
DOI: 10.1186/s12864-018-5158-z
sha: ecf90eb55cfef5b0212b52caf031abb31a1f11cc
doc_id: 799500
cord_uid: 93ldjyi5

BACKGROUND: Long non-coding RNAs (lncRNAs) are involved in variable cleavage, transcriptional interference, regulation of DNA methylation and protein modification. However, the regulation of lncRNAs in plant somatic embryos remains unclear. The longan (Dimocarpus longan) somatic embryogenesis (SE) system is a good system for research on longan embryo development. RESULTS: In this study, 7643 lncRNAs obtained during early SE in D. longan were identified by high-throughput sequencing, among which 6005 lncRNAs were expressed. Of the expressed lncRNAs, 4790 were found in all samples and 160 were specifically expressed in embryogenic callus (EC), 154 in incomplete embryogenic compact structures (ICpECs), and 376 in globular embryos (GEs). We annotated the 6005 expressed lncRNAs, and 1404 lncRNAs belonged to 506 noncoding RNA (ncRNA) families and 4682 lncRNAs were predicted to target protein-coding genes. The target genes included 5051 cis-regulated target genes (5712 pairs) and 1605 trans-regulated target genes (3618 pairs). KEGG analysis revealed that most of the differentially expressed target genes (mRNAs) of the lncRNAs were enriched in the “plant-pathogen interaction” and “plant hormone signaling” pathways during early longan SE. Real-time quantitative PCR confirmed that 20 selected lncRNAs showed significant differences in expression and that five lncRNAs were related to auxin response factors. Compared with the FPKM expression trends, 16 lncRNA expression trends were the same in qPCR. In lncRNA-miRNA-mRNA relationship prediction, 40 lncRNAs were predicted to function as eTMs for 15 miRNAs and 7 lncRNAs were identified as potential miRNA precursors. In addition, we verified the lncRNA-miRNA-mRNA regulatory relationships by transient expression of miRNAs (miR172a, miR159a.1 and miR398a). CONCLUSION: Analyses of lncRNAs during early longan SE showed that differentially expressed lncRNAs were involved in expression regulation at each SE stage, and may form a regulatory network with miRNAs and mRNAs. These findings provide new insights into lncRNAs and lay a foundation for future functional analysis of lncRNAs during early longan SE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5158-z) contains supplementary material, which is available to authorized users.

The long noncoding RNAs (lncRNAs), which are noncoding RNAs over 200 nt in length, are devoid of open reading frames (ORFs) and are mainly transcribed by RNA polymerase II (Pol II). lncRNAs are spliced and have a cap structure with a poly A tail, lncRNAs have lower expression levels of sequence conservation than protein-coding mRNAs [1] . lncRNAs come from the intergenic, intronic or coding gene regions in the sense and antisense directions. According to their genomic transcriptional positions, lncRNAs can be grouped into three classes: antisense, intronic, and intergenic. It has been reported that lncRNAs play important regulatory roles at the gene transcriptional [2] , post-transcriptional [3] , translational [4] and epigenetic [5, 6] levels, and are involved in variable cleavage, transcriptional interference, regulation of DNA methylation and protein modification. Interactions between lncRNAs and microRNAs (miRNAs) are also widespread. Cai et al. (2007) identified an endogenously expressed 23-nt miRNA derived from lncRNA H19 in human keratinocytes and neonatal mice, and demonstrated that H19 could be used as a primary miRNA precursor [7] . Moreover, some lncRNAs have miRNA-binding sites and can function as endogenous target mimics (eTMs) of miRNAs [8] . In regard to embryogenesis, some lncRNAs identified in mice were found to not only be controlled by embryonic stem cell transcription factors but also regulated by the mice embryonic development status [9] . In plants, lncRNAs have been found to regulate growth and development [10] , reproductive development [11] and stress responses [12] . However, while there have been a few reports on the regulation of lncRNAs in animal embryos, studies on lncRNAs in plant somatic embryogenesis (SE) have not been reported to date.

Longan (Dimocarpus longan Lour.) is an important fruit tree that originated in southern China and Vietnam, and has a wealth of pharmacological uses such as in antioxidants, hypoglycemic drugs and nervous system regulators [13] besides supplying fruit. Longan embryo development largely influences seed size, fruit set, fruit quality and yield. In-depth embryological studies of longan are of great significance for the longan industry [14] . A longan SE system established by Lai et al. [15] is considered an excellent model systems for woody plants SE. Recently, our laboratory has conducted systematic research on non-coding RNAs during early longan SE, mainly focusing on miRNAs. A total of 643 conserved and 29 novel miRNAs (including star strands) of 169 miRNA families were identified during longan SE [16] . The molecular mechanisms of miR167 [17] , miR390 [18] and miR160 [19] in the regulation of the auxin response factors were demonstrated in longan SE. In addition, miR159 family members [20] and miR171 [21] , which are involved in flower organ formation, were found to have the most stable expression among miRNAs at different developmental stages of longan SE [22] . In 2013, our laboratory constructed a cDNA library from a longan friable-embryogenic callus RNA sample and a large number of specific genes were identified [23] . All of these studies were focused on miRNAs and mRNAs in longan. Now, however, with the release of longan genome data from our laboratory [24] , investigation of the regulatory roles of lncRNAs in longan SE has become possible. Therefore, based on the longan SE system and Illumina HiSeq sequencing platform, we isolated and identified lncRNAs from three samples of early longan SE, i.e., embryogenic callus (EC), incomplete embryogenic compact structures (ICpECs), and globular embryos (GEs). We explored the functions of the lncRNAs and their target genes in the three samples and speculated that lncRNAs might participate in the developmental process, and then predicted the regulation of lncRNAs, miRNAs and lncRNAs during early longan SE. Finally, qPCR assays and transient overexpression or inhibition of expression techniques were used to validate key lncRNAs, miRNAs and mRNAs. The results enhance our understanding of the regulation of lncRNAs and provide valuable information for research on lncRNAs during early longan SE.

To investigate the regulatory roles of lncRNAs during early longan SE, lncRNAs obtained from EC, ICpEC and GE samples of longan were sequenced by Illumina HiSeq sequencing. An average of 195,823,419 original sequences were obtained per sample. From 12.69 Gb data, 45,124 transcripts were detected among the clean reads. We distinguished between mRNAs and lncRNAs based on transcriptional codes. In total, 7643 novel lncRNAs, 16,162 novel mRNAs, and 31,007 known mRNAs were identified (Additional file 1); all lncRNAs identified in our research were novel lncRNAs.

It has been reported that compared with proteincoding genes, lncRNAs are shorter and have smaller numbers of exons in plants [25] . The length and exon number distributions of the 7643 lncRNAs in all three early stages of SE were compared with those of all 47,169 predicted mRNAs. The results showed that 83.04% of lncRNAs were 0-2000 bp, 12.64% were 2000-4000 bp, and only 4.32% were > 4000 bp in length, By contrast, 7.19% of mRNAs were > 4000 bp, 65.13% were 0-2000 bp, and 25.64% were 2000-4000 bp in length (Fig. 1a) . Notably, 74.39% of lncRNAs in the early longan SE samples contained only one or two exons, whereas the number of exons in 82.41% of the mRNAs ranged from 1 to 10. In contrast to protein-coding genes, the lncRNAs had a smaller number of exons (Fig. 1b) .

RNA-Seq expression analysis revealed that among the 7643 lncRNAs and 47,169 mRNAs identified, 6005 novel lncRNAs, 15,233 novel mRNAs, and 23,886 known mRNAs were expressed in the three samples. Of the 6005 expressed lncRNAs, 5254 were detected in the EC stage, 5320 in the ICpEC stage, and 5568 in the GE stage. Additionally, 4790 lncRNAs were shared among the three samples and 160 lncRNAs were specifically expressed in EC, 154 in ICpEC, and 376 in GE. The number of lncRNAs and specific lncRNAs identified at the GE stage was the highest (Fig. 1c) .

According to the locations of the nearest protein coding genes, 3422 of the 6005 expressed lncRNAs were classified into three categories: intergenic lncRNAs without any overlap with protein-coding genes, intragenic lncRNAs positioned in protein-coding loci, and antisense lncRNAs overlapping with exons of a protein-coding transcript on the opposite strand [26, 27] . Of the 3422 lncRNAs, 93.37% were intergenic, 0.38% were intragenic, and 6.25% were antisense (Fig. 1d) .

lncRNAs are divided into distinct ncRNA families based on the evolutionarily conserved secondary structure of the RNA, the cis-acting elements of mRNA, other RNA elements, and the common ancestors of ncRNAs. We annotated 6005 lncRNAs (Additional file 2), among which 1404 lncRNAs belonged to 506 ncRNA families, with 1766 groups (a lncRNA could be annotated as belonging to multiple families). Of these 1766 groups, 53.63% were annotated as miRNA families, 25.50% as snoRNA families, and 4.99% as sRNA families. Only 5.06% were annotated as lncRNAs families, including the oxidative stress-induced adapt33 family [28, 29] , the DLX6 family involved in embryonic organogenesis [30] and the methylated KCNQ1OT1-1 family [31] . The remaining groups were annotated as the virus-associated families Corona-pk3 [32] , flavi-FSE [33] and HIV [34] .

In this study, we detected 39,119 genes encoding proteins associated with longan SE in three samples, and determined the expression levels of these genes by Fragments per Kilobase per Million (FPKM) mapped reads values. Large-scale expression profiling through FPKM values showed that the number of differentially expressed mRNAs was 3877 in EC vs. ICpEC, 7746 in ICpEC vs. GE and 9222 in EC vs. GE. Compared with EC, 5317 mRNAs were up-regulated and 3905 mRNAs were down-regulated in GE, and 2057 mRNAs were up-regulated and 1820 mRNAs were down-regulated in ICpEC. Compared with ICpEC, 4728 mRNAs were up-regulated and 3018 mRNAs were down-regulated (Fig. 2a) .

In the significant difference analysis of the 6005 lncRNAs, we found that the number of significantly differentially expressed lncRNAs in EC vs. GE was greater than that in EC vs. ICpEC and ICpEC vs. GE (Fig. 2b) . During early longan SE, 1259 and 335 lncRNAs were significantly expressed in EC vs. GE and EC vs. ICpEC, respectively. Compared with EC, 802 of 1259 lncRNAs were up-regulated and the other 457 lncRNAs were down-regulated in GE, and 229 of 335 lncRNAs were up-regulated and the other 106 lncRNAs were down-regulated in ICpEC. There were 1028 significantly differentially expressed lncRNAs in ICpEC vs. GE. Compared with ICpEC, 604 of the 1028 lncRNAs were up-regulated and the other 424 lncRNAs were down-regulated in GE.

The lncRNAs showed different expression trends during longan early SE according to the FPKM values. In this study, the expression of 3680 lncRNAs over time was analyzed based on their expression levels in different SE stages to identify expression trends. As shown in Fig. 2c , the expression trends of the 3680 lncRNAs in the three samples were divided into nine major categories. The expression levels of 273 lncRNAs, which accounted for 7.42% of the total lncRNAs, from the first category were lower in the ICpEC stage than in the EC and GE stages. The lncRNAs in the fifth (386 lncRNAs) and seventh (361 lncRNAs) categories were expressed at higher levels in the ICpEC stage than in the other stages. The lncRNAs in the second and fourth categories showed stable expression from the EC to ICpEC stage. The second category included 369 lncRNAs (9.89% of the total) whose expression decreased in the GE stage. The fourth category contained 688 lncRNAs (18.70% of the total) whose expression increased in the GE stage. The third and sixth categories showed two completely opposite trends: the 477 lncRNAs (12.96% of the total) classified into the third category exhibited higher expression levels in the GE stage, whereas the 340 lncRNAs (9.24% of the total) classified into the sixth category showed higher expression levels in the EC stage. The lncRNAs in the eighth and ninth categories showed stable expression from the ICpEC to the GE stage, but the 417 lncRNAs (11.33% of the total) classified into the eighth category exhibited lower expression levels in the EC stage, while the 373 lncRNAs (10.14% of the total) classified into the ninth category exhibited higher expression levels in the EC stage. The lncRNAs in the second, fourth, and eighth categories were accumulated from the EC to the GE stage, indicating that the related lncRNAs in these three categories contributed to the formation of the GE stage. The expression decrease from the EC to GE stage in the sixth and ninth categories indicated that the lncRNAs in these two categories were mainly involved in the maintenance of the EC stage. The lncRNAs in the second, fifth and seventh categories were highly expressed in the ICpEC stage, and these lncRNAs were possibly involved in ICpEC morphogenesis. The specific lncRNA data for early longan SE suggested the lncRNAs were involved in regulation at each SE stage.

The potential target genes of the lncRNAs were predicted according to their regulatory methods, which were divided into cis-and trans-regulation. Of the 6005 lncRNAs, only 4682 lncRNAs were predicted to target protein-coding genes, including 5051 cis-regulated target genes (5712 pairs) and 1605 trans-regulated target genes (3618 pairs) (Additional file 3).

Among the potential target genes (mRNAs) of the lncRNAs, 852 genes were deferentially expressed in EC vs. GE (Additional file 4), with 558 up-regulated and 294 down-regulated. There were 538 differentially expressed genes in ICpEC vs. GE, among which 384 were up-regulated and 154 were down-regulated. The number of differentially expressed genes in EC vs. ICpEC was 99, among which 34 were up-regulated and 55 were down-regulated. Gene Ontology (GO) analysis was performed to investigate the differentially expressed target genes in the EC, ICpEC and GE stages (Fig. 3) ; an FDR ≤ 0.01 was considered to indicate significant enrichment. Only the cellular component genes were enriched in EC vs. ICpEC. In ICpEC vs. GE, a total of 31, 9, and 8 genes were assigned to the biological process, cellular component, and molecular function categories, respectively. In EC vs. GE, genes in the biological process, cellular component, and molecular function categories were also enriched. In the biological process category, 32 terms including protein phosphorylation, RNA metabolic process, and transport were significantly enriched, while in the cellular component category, the top three terms were membrane, protein complex, and nucleus. In the molecular function category, kinase activity, transferase activity/ transferring phosphorus-containing terms and ATP binding were the most abundant terms.

We further categorized the 39,119 differentially expressed potential target genes (mRNAs) using Kyoto Encyclopedia of Genes and Genomes (KEGG) (Additional file 5). The results indicated that 51 potential target genes were enriched in 23 pathways in EC vs. ICpEC; the top five most enriched pathways were as follows: linoleic acid metabolism, steroid biosynthesis, aminoacyl-tRNA biosynthesis, ubiquitin mediated proteolysis, and base excision repair. In ICpEC vs. GE, 424 potential target genes were enriched in 77 pathways and the top five most enriched pathways included: plant-pathogen interactions, plant hormone signaling, glyoxylate and dicarboxylate metabolism, homologous recombination, and brassinosteroid biosynthesis. Additionally, 686 potential target genes were enriched in EC vs. GE; the EC to the GE stage is the general period of early development of longan SE. Among all 89 enriched KEGG pathways, 92 potential target genes of lncRNAs were related to "plant-pathogen interaction" and 30 target genes were related to "plant hormone signaling". The top five most enriched pathways included: plant-pathogen interaction, plant hormone signal transduction, sulfur metabolism, homologous recombination and linoleic acid metabolism. Plant-pathogen interaction, plant hormone signal transduction, homologous recombination, and linoleic acid metabolism were significantly affected during the ICpEC and GE stages compared with the EC stage. Five genes related to auxin response factors that were targeted by lncRNAs were identified: an auxin (AUX) gene targeted by LTCONS-00006334; auxin response factor (ARF) genes targeted by LTCONS-00025525, LTCONS-00030223, and LTCONS-00055024; and an auxin-responsive protein IAA (AUX/IAA) gene targeted by LTCONS-00008111. These targets of differentially expressed lncRNAs, therefore, were considered to play fundamental roles in early longan SE.

To confirm the significant differences in the expression of lncRNAs and their predicted target genes in early longan SE, 20 lncRNAs with significant differences in expression were selected from among 641 up-regulated and 316 down-regulated lncRNAs in the RNA-Seq data. Additionally, 11 potential target genes (mRNAs) and five lncRNAs related to auxin response factors were verified by qPCR in the three stages of early longan SE. Twenty-four of the lncRNAs were detected in EC, ICpEC and GE (excluding LTCONS-00027337).

Cluster analysis of the expression patterns of the 24 lncRNAs in qPCR (Fig. 4a) and RNA-Seq (Fig. 4b) , and qPCR of nine selected lncRNAs (Fig. 4c) was performed during early longan SE. The expression patterns of the 24 lncRNAs were divided into three categories according to the timing of their highest expression level. In category I, eight lncRNAs exhibited high levels in the EC stage, but low levels in the other two stages. LTCONS-00022673, LTCONS-00057369, LTCONS-00031251 and LTCONS-00008111 showed a decrease in expression from the ICpEC to GE stage, which indicated that their expression levels decreased gradually during longan SE, while the expression levels of LTCONS-00030223, LTCONS-00006334, LTCONS-00045113 and LTCONS-00013909 did not change much from the ICpEC to GE stage. In category II, four lncRNAs had the highest expression in the ICpEC stage. The expression levels of LTCONS-00030919 and LTCONS-00045469 in the EC and GE stages were basically unchanged. The expression levels of LTCONS-00029834 and LTCONS-00055024 in the EC stage were higher than in the GE stage. In category III, the expression of the 12 lncRNAs was highest in the GE stage; the expressions of LTCONS-00038577 and LTCONS-00010999 decreased gradually from the EC to ICpEC stage, while that of LTCONS-00031272, LTCONS-00025525, LTCONS -00038201, LTCONS-00027338 and LTCONS-00031543 did not change much at the EC and ICpEC stages. The expressions of LTCONS-00053938, LTCONS-00050060, LTCONS-00022307, LTCONS-00037848 and LTCONS-00021462 increased gradually from EC to ICpEC. These results indicated that different lncRNAs might be involved in the maintenance of different stages of longan SE, i.e. the eight lncRNAs of category I could be related to maintaining the pre-embryonic status of the EC, the four lncRNAs of category II could be related to maintaining the embryogenic status of the ICpEC, and the 12 lncRNAs of category III could be related to maintaining the embryonic status of the GE.

Comparing the expression trends of the lncRNAs in qPCR (Fig. 4a) with those in RNA-Seq (Fig. 4b) showed that the expression trends of 16 of the 24 lncRNAs were the same. The inconsistencies of the other eight lncRNAs were as follows: LTCONS-00053938 showed highest expression in the GE stage and the lowest expression in the EC stage according to qPCR, but its expression was lowest in the GE stage and highest in the EC stage in RNA-Seq. The expression level of LTCONS-00010999 decreased from the EC to ICpEC to GE stage in qPCR, but increased from the EC to ICpEC to GE stage in RNA-Seq. The expression of LTCONS-00031272 in the GE stage was higher in qPCR than in RNA-Seq. For LTCONS-00030223, LTCONS-00006334 and LTCONS-00045113, the expression in qPCR was highest in the EC stage and in RNA-Seq was highest in the GE stage. The expression of LTCONS-00055024 and LTCONS-00045469 was highest in the ICpEC stage in qPCR, but highest in the GE stage in RNA-Seq.

In the qPCR analysis of 11 lncRNAs and their potential target genes (mRNAs), except for LTCONS-00013909 and the target gene MTCONS-00013943 of LTCONS-00027337, all of the lncRNAs and their target genes were detected (Fig. 4c) . According to the expression patterns of the lncRNAs and their target genes mRNAs, LTCONS-00022307, LTCONS-00045469 and LTCONS-00010999 were found to target cis mRNAs 20 kbp downstream (cis mRNA dw20k), while LTCONS-00029834, LTCONS-00022673, LTCONS-00037848 and LTCONS-00038201 were trans-acting, and LTCONS-00050060 and LTCONS-00031543 targeted cis mRNAs 10 kbp upstream (cis mRNAs up10k). Among the three cis mRNA dw20k-type lncRNAs, only LTCONS-00022307 negatively regulated its potential target genes during early longan SE; the other two lncRNAs were positive regulators. Among the four trans-acting lncRNAs, LTCONS-00022673, LTCONS-00037848 and LTCONS-00038201 had a significant positive correlation with their target genes. Of the two cis mRNAs up10k lncRNAs, LTCONS-00031543 had a positive regulatory effect on its target gene. From the above results, we deduced that the regulation of target genes by the lncRNAs did not entirely depend on the positional relationship between the lncRNAs and their target genes.

Functions of lncRNAs in the lncRNA-miRNA expression network in longan early SE There were a large number of differentially expressed miRNAs and lncRNAs in longan SE, so to study the regulatory roles of lncRNAs in longan SE, we focused on three aspects, including lncRNAs acting as eTMs for miRNAs, lncRNAs acting as precursors to miRNAs and lncRNAs as miRNA target genes.

As a new type of regulatory factor, eTMs play an important regulatory role in the process of plant cell differentiation and development [25, 35] . By binding a miRNA, an eTM blocks miRNA cleavage and thus isolates the miRNA from its target mRNAs. In the present work, 40 lncRNAs were predicted to function as eTMs for 15 miRNAs (Fig. 5b) with TAPIR. Based on their sequence conservation, these 15 miRNAs came from 15 different miRNA families, including miR403, miR406 and miR400. Because miRNAs have a significant regulatory effect on their target mRNAs, we speculated that the lncRNAs acting as eTMs for miRNAs during early longan SE could greatly affect the miRNA regulatory network.

Genome-wide studies have shown that a significant fraction of lncRNAs may function as precursors of small RNAs < 200 nucleotides (nt) in length. Of the 7643 predicted lncRNAs, seven were identified as potential miRNA precursors of three families (Table 1) . LTCONS-00010286, LTCONS-00010359 and LTCONS-00010360 might serve as precursors of the miR162 family, LTCONS-00022889 was predicted to be a precursor of the miR319 family, and LTCONS-00025684, LTCONS-00025685 and LTCONS-00032074 might serve as precursors to the miR156 family. During target gene prediction and annotation for these seven lncRNAs, only LTCONS-00025685 and LTCONS-00032074 were found to have potential target mRNAs, which were annotated as TFIID and eukaryotic initiation Factor 4A-11.

Some of the lncRNAs responding to early longan SE might be regulated as targets by miRNAs. The "psRNA-Target" program (expectation ≤5) was used to predict the possible roles of miRNA targets among the 7643 lncRNAs (Additional file 6). In total, 1765 lncRNAs were predicted to be targets of 85 miRNAs in 74 families. One lncRNA could be targeted by multiple miRNAs. For example, LTCONS-00000242 was targeted by miRNAs belonging to six different families. Conversely, one miRNA could also target multiple lncRNAs, e.g. Dlo-miR1436 was predicted to target 182 different lncRNAs. Based on the above predictions, a miRNA targeting regulatory network for the lncRNAs was constructed (Fig. 5a) , and it was speculated that a large number of lncRNAs were regulated as targets of miR-NAs during early longan SE.

Studies have shown that auxin plays a regulatory role in plant embryogenesis and regulates embryo development via the regulation of auxin-responsive transcription [36, 37] . In KEGG enrichment analysis of the 39,119 differentially expressed potential target genes during the early development of longan SE, 30 differentially expressed genes (5.33% of genes annotated to the pathway) in EC vs. GE, 2 differentially expressed genes (2.67%) in EC vs. ICpEC, and 31 differentially expressed genes (8.33%) in ICpEC vs. GE were enriched in the phytohormone signaling pathway. Five target genes in the auxin signaling pathway were identified by lncRNA target gene prediction, including ARF4 targeted by LTCONS-00025525, IAA6 and AUX22 targeted by LTCONS-00008111, ABF targeted by LTCONS-00030223 and LTCONS-00055024, and AUX2 targeted by LTCONS-00006334 (Fig. 5c) .

To profile the expression patterns of the lncRNAs associated with auxin response factors, five lncRNAs, their target genes (auxin response factors) and the corresponding miRNAs were analyzed by qPCR in EC, ICpEC and GE (Fig. 6) . Although there were some differences in expression levels, the qPCR and RNA-Seq data showed the same changes trends. The qPCR results showed that LTCONS-00025225 regulated ARF4 and LTCONS-00055024 regulated ABF5-1, both of which were cis mRNA up10k types and were highly expressed in GE. LTCONS-00006334 regulated AUX2 and LTCONS-00008111 regulated IAA6/AUX22, and these target genes were cis mRNA dw20k types. LTCONS-00030223 regulated ABF5-5, which was an overlapping cis mRNA, and both were highly expressed in EC. While there was a negative regulatory relationship between LTCONS-00006334 and its target gene, the other four lncRNAs positively regulated their target genes. Thus, lncRNAs with different modes of action were involved in the auxin signaling pathway, with different potential target genes and corresponding differential expression patterns in different stages of longan SE, which indicated that lncRNAs were involved in the auxin signaling pathway through complex regulatory mechanisms.

In summary, the lncRNA-miRNA-mRNA regulatory network in the auxin signaling pathway was constructed from lncRNAs, miRNAs and mRNAs, and verified by qPCR of five lncRNAs and related miRNAs (Additional file 7). The results showed that only related miRNAs were differentially expressed during the early development of longan SE, including Dlo-miR157d, which was related to LTCONS-00025525 targeting ARF4, Dlo-miR482a and Dlo-miR482a, which were related to LTCONS-00030223 targeting ABF5-5, and miR172a, Dlo-miR417, Dlo-miR162a * , and Dlo-miR806a, which were associated with LTCONS-00055024 targeting ABF5-1. The remaining miRNAs showed no significant difference during early longan SE.

Overexpression and inhibition of miR172a, miR159a.1 and miR398a in longan embryogenic callus After predicting the relationships between lncRNAs, miR-NAs and mRNAs, three networks of miRNAs closely Fig. 5 Prediction of lncRNA-miRNA-mRNA relationships in early longan SE. a In total, 1765 lncRNAs were predicted as targets of 85 miRNAs by psRNATarget (expectation ≤5). b Forty lncRNAs were predicted to function as eTMs for 15 miRNAs by TAPIR. c Five lncRNAs involved in auxin response factor mRNA and miRNA networks. The black arrows indicate relationships between lncRNAs and miRNAs and the red arrows indicate relationships between lncRNAs and mRNAs related to SE (miR172a, miR159a.1 and miR398a) were selected for qPCR verification in longan. In the miR172a network, LTCONS-00042843 targeted Dlo-018542.1 and acted on miR172a as an eTM (Fig. 7a) . The expression of Dlo-miR172a tended to be stable during the early stages of longan SE with no significant changes. However, the expressions of LTCONS-00042843 and Dlo-018542.1 was significantly different in ICpEC and GE compared with the EC stage. LTCONS-00042843 had the highest expression level at the ICpEC stage, while Dlo-018542.1 had the highest expression level at the GE stage (Fig. 7b) . Expression comparisons between LTCONS-00042843 and Dlo-018542.1 under overexpression and inhibition of miR172a in longan EC were conducted, and the results showed that the expression of LTCONS-00042843 and Dlo-018542.1 decreased when Dlo-miR172a was overexpressed but increased when Dlo-miR172a expression was inhibited compared with the control check (CK) (Fig. 7c) , which was consistent with the predicted relationships among lncRNAs, mRNAs and miRNAs in longan SE. and indicated that inter-regulation among them might exist.

In the miR159a.1 network (Additional file 8), LTCONS-00046326 was predicted to be a Dlo-miR159a.1 target gene and to act as an eTM for Dlo-miR529d, and both Dlo-017525.1 and Dlo-028266.1 were predicted to be target genes of LTCONS-00046326. Surprisingly, both overexpression and inhibition of Dlo-miR159a.1 promoted the expression of the target gene LTCONS-00046326, implying the existence of a complicated regulatory network of lncRNA, miRNA and mRNA.

In the miR398a network (Additional file 9), Dlo-miR398a acted on the target genes LTCONS-00032074 and LTCONS-00039356, which in turn acted as eTMs for Dlo-miR157d and Dlo-miR406, respectively. Using primers targeting different sites, it was found that the expression level of LTCONS-00039356, a target gene of Dlo-miR398a, was not significantly different from that of CK under overexpression and inhibition of Dlo-miR398a in longan EC; however, LTCONS-00039356, as an eTM of Dlo-miR157d and Dlo-miR406, showed significantly different expression compared with CK. There was a significant change in response tendencies with overexpression and inhibition of Dlo-miR398a in longan EC, but Dlo-miR157d and Dlo-miR406 showed no significant response trends in the same material. The above results shows that lncRNAs bound to miRNAs at different binding sites and had different expression in the same material.

Longan may require a large amount of lncRNA to initiate GE formation

Many researchers have focused on lncRNAs in recent years, and remarkable progress has been made, especially in human and animals [38] . Conversely, studies on lncRNAs in plants are still in their infancy, and most have focused on crops such as model plants [11, 39] and rice [40] . In total, 74.39% of the lncRNAs involved in the early stages of longan SE had only one or two exons, which might account for their low expression levels. The conservation of lncRNAs among species is poor, which also hinders research on lncRNAs. It has been reported that lncRNAs play a regulatory roles by acting on protein-coding genes [44, 45] . Therefore, differential enrichment analysis of the target genes (protein-coding genes) of lncRNAs during early longan SE provided valuable information. In this study, the plant-pathogen interaction, plant hormone signaling, sulfur metabolism and various kinds of amino acid metabolism pathways were revealed to be closely related to early longan SE. Of the top five most enriched pathways, three were commonly enriched in EC vs. GE and ICpEC vs. GE, and the number of differentially expressed lncRNAs in ICpEC vs. GE was 4.55 times that in EC vs. ICpEC. These results indicate that similar molecular mechanisms are active between the pre-embryonic EC and the embryogenic ICpEC, and the main change leading to GE formation occurs in the ICpEC to GE stages. Thus, it can be seen that the molecular mechanisms of embryo formation can change dramatically. Previous studies reported that the plant-pathogen interaction pathway was enriched in lncRNAs [46] , miR-NAs [47, 48] and gene transcripts [23] , which suggested the importance of plant-pathogen interactions in the embryonic developmental network in longan and other plants. Plant hormones play important roles in plant growth and SE in plants [49] . In a study of SE of Hevea seeds, it was found that an excess of auxin and cytokinin inhibited the embryogenic ability of callus [50] . Zhu et al. studied the effects of plant hormones on SE and plant regeneration in cassava (Manihot esculenta Crantz) [51] . The phytohormone signal transduction pathway includes auxin, kinetin, gibberellin and abscisic acid, among which auxin is an important factor in plant SE, e.g. it regulates embryonic development by regulating ARF-mediated transcription [36, 37] , and Aux/IAAs also participate in the regulation of auxin by inhibiting ARF-mediated transcription [52] . Our laboratory has studied related genes including TIF1 [53] , DlARF8 [17] , ARF3/4 [18] and ARF10, − 16, and − 17 [19] that regulate the auxin response. In the KEGG enrichment results, it seemed that longan had begun to establish disease resistance mechanisms and other metabolic components based on hormones in the GE stage. This change not only involved a large number of mRNAs, but also a large number of lncRNAs that participate in the molecular regulation and morphogenesis of the GE stage by regulating target genes (mRNA). lncRNAs regulate the expression of target genes in cis or trans through a variety of mechanisms. Previous studies have shown that cis regulation by lncRNAs includes enhancer activity [54] and insulator functions [55] . A common method of trans-regulation is the upregulation of target gene expression by forming dimers with neighboring mRNAs that increase mRNA stability [56, 57] . In this study, the locations of 14 pairs of lncRNAs and their target mRNAs were verified by qPCR analysis. Ten pairs of cis-regulated mRNAs and lncRNAs were identified, including seven pairs that had positively regulated and three pairs that had negatively regulated genes. Four pairs of trans-regulated mRNAs and lncRNAs were found in longan SE, including three pairs with positive regulatory relationships and one pair with a negative regulatory relationship. The target genes of the five lncRNAs associated with auxin response factors were cis-regulated, which implied that the lncRNAs associated with auxin response factors mainly function as cis-acting regulators during early longan SE.

lncRNAs acting as eTMs for miRNAs may be an important regulatory mechanism during longan early SE lncRNAs were observed to function as eTMs for miR-NAs, revealing a new mechanism for the regulating of miRNAs by lncRNAs in plants. lncRNAs bind to miR-NAs as endogenous trapping targets of miRNAs and reduce the miRNAs' function to inhibit target expression. In Arabidopsis, the lncRNAs IPS1 bound to ath-miR399 and a three-nucleotide bulge was formed between the 10th and 11th positions of the 5 'end to prevent the cleavage of IPS1 by ath-miR399 [11] . In addition, miR160a* largely interacted with its predicted eTMs during the GE and EC stages [19] , and the interaction between miR172 and eTMs could delay flowering and eliminate top-of-the-range benefits [58, 59] . MiRNAs and their predicted eTMs have also been reported during longan SE: miR167 cleaved the DlARF8 mRNA during longan SE [17] , and an eTM down-regulated miR167, and the regulation of miR160 and its predicted eTM were involved in hormone signaling in longan [19] .

In our study, 40 lncRNAs were predicted to function as eTMs for 15 miRNAs and four lncRNAs were validated as eTMs of four miRNAs (Dlo-miR172a, Dlo-miR529d, Dlo-miR157d, and Dlo-miR406). LTCONS-00042843, LTCONS-00046326, LTCONS-00032074, and LTCONS-00039356 were respectively identified as eTMs for Dlo-miR172a, Dlo-miR529d, Dlo-miR157d, and Dlo-miR406. Additionally, the qPCR results showed that LTCONS-00042843 and LTCONS-00046326 inhibited the expression of Dlo-miR172a and Dlo-miR529d, respectively. Our study is the first to discover that lncRNAs act as eTMs of miR172a and miR529d in the EC stage in longan.

Multiple regulatory mechanisms may exist among lncRNA, miRNA and mRNA during early SE in longan

In addition to the above lncRNAs acting as eTMs for miRNAs, lncRNAs may also interact with miRNAs as miRNAs precursors and act as miRNAs target genes. During the early stages of longan SE, only seven lncRNAs were predicted to be precursors of miRNAs (miR156 family, miR319 family and miR162 family). In longan SE, members of the Dlo-miR156 family were associated with different developmental stages of early embryo cultures [16] , and Dlo-miR162 regulated specific stages of SE through multiple miRNAs [60] . miR319b.1 was significantly accumulated at the cotyledon stage in lily SE [61] . In addition, miR156 regulated rice seed and pollen development [62] , miR319 affected leaf development in Arabidopsis [63] and participated in rice stress responses [64] , and miR162 might be involved in gene expression regulation and cotyledon formation during germination in Asteraceae. Functional annotation of target genes predicted for the lncRNAs suggested that Dlo-015497.1 and Dlo-019109.1 might be involved in transcriptional initiation as transcription initiation factors. Based on the functions of miRNAs and mRNAs in longan and other plants, we speculate that some lncRNAs are involved in regulation of gene expression by acting as miRNA precursors during early longan SE.

In the present work, based on miRNA target prediction, 1765 lncRNAs were predicted to be targets of 85 miRNAs of 74 families. Thus, the majority of lncRNAs regulation might be achieved via miRNAs during early longan SE, and lncRNAs might indirectly regulate the expression of mRNAs by regulating the number of miR-NAs. Five lncRNAs related to the auxin response factors selected for miRNA target prediction, and seven miR-NAs (lncRNAs as miRNA target genes) were predicted to be involved in the action of lncRNAs. Notably, both lncRNAs and t protein-coding genes could act on the same miRNA at the same time. For example, LTCONS-00030223 and MTCONS-00030224 are both target genes for Dlo-miR810b, Dlo-miR482a, Dlo-miR417 and Dlo-miR172a, and MTCONS-00030224 was predicted to be a target gene for LTCONS-00030223. Additionally, LTCONS-00055024 was a target gene for three miRNAs (Dlo-miR160a, Dlo-miR1774b and Dlo-miR806a). Studies have shown that dlo-miR160a targets DlARF10, − 16 and − 17 [19] . The target gene MTCONS-00055015 (ABF-5) of LTCONS-00055024 also regulates hormone signal transduction. Therefore, we speculate that LTCONS-00055024, MTCONS-00055015 and Dlo-miR160a might exist in a regulatory network.

To verify the relationships among lncRNAs, miRNAs and mRNAs during the early development of longan SE, qPCR was performed on Dlo-miR172a, Dlo-miR159a.1 and Dlo-miR398a. Through qPCR analysis of the EC samples with Dlo-miR172a, Dlo-miR159a.1 and Dlo-miR398a overexpression and inhibition, we found regulatory interactions of Dlo-miR172a and the corresponding lncRNA and mRNA during early SE in longan. However, the regulating relationshipS among Dlo-miR398a, Dlo-miR159a.1 and the corresponding mRNAs and lncRNAs were complicated and needed to be further explored.

In this study, 6005 expressed lncRNAs were identified during the early stage of SE in longan. The number of lncRNAs specifically expressed in the GE stage was much greater than that in the EC stage and the ICpEC stage. We speculate that the GE stage requires more lncRNAs to regulate. The most highly enriched KEGG pathways were plant-pathogen interactions and phytohormone signaling. qPCR verification of five ARFrelated lncRNAs and their target genes (mRNA) suggested that lncRNAs tend to positively regulate target genes in the early stages of longan SE. In lncRNA-miRNA-mRNA relationship predictions, some lncRNAs were predicted to function as eTMs for miR-NAs and some were identified as potential miRNA precursors. In addition, we verified the lncRNA-miRNA-mRNA regulatory relationships by transient expression, and speculate that they comprise a regulatory network. Our results contribute to the understanding of lncRNA regulation in plant SE.

Synchronized embryogenic cultures at different developmental stages, consisting of friable-embryogenic callus (EC), incomplete compact pro-embryogenic cultures (ICpEC) and globular embryos (GE) were obtained following previously published methods for longan [15, 65] . The plant materials were stored at − 80°C for later use.

RNA samples were extracted from the three abovementioned cultures using Trizol reagent (Invitrogen, Carlsbad, CA, USA). The RNA was detected with an Agilent 2100 detection kit and the NanoDrop assay. The integrity of RNA was detected by 1.0% non-denaturing agarose gel electrophoresis. After the quality and concentration were checked, cDNA strands were synthesized with random primers and reverse transcriptase from the TruSeq® Stranded kit, and double-stranded cDNA was synthesized and amplified by using DNA polymerase I and RNaseH to obtain cDNA libraries. Raw reads were obtained using the Illumina HiSeq sequencing platform, and low-quality reads (quality Q ≤ 10 bases accounted for > 50% of the entire read), adapter contamination, and reads with a high content of N (containing an N ratio > 10%) were removed to get clean reads.

The clean reads were aligned to the longan reference genome [24] using the alignment software HISAT [66] for transcript assembly, and transcripts with lower expression (FPKM ≤0.5) and lengths below 200 bp were filtered out. The transcripts were identified as mRNAs or lncRNAs by using the software programs CPC [67] , txCdsPredict and CNCI [68] , and the Pfam database [69] . Inter-sample differential analysis of the obtained lncRNAs was carried out using the differential analysis method PossionDis [70] (fold change ≥2.00 and FDR ≤ 0.001), and by comparing the expression of the samples, genes with insignificant changes in expression were excluded and genes with significant differences were retained. The lncRNAs families were analyzed with NFERNAL [71] , which annotates lncRNAs to families by aligning them to the Rfam database. The expression of the three samples was analyzed as a time series according to previous studies [72, 73] .

The potential target genes of the lncRNAs were predicted according to their regulatory methods, which were divided into cis-and trans-acting. The basic principle for the prediction of cis target genes is that the functions of lncRNAs are related to the protein coding genes near their coordinates [74] . Therefore, the neighboring mRNAs of lncRNAs were screened as target genes. Trans regulation is not dependent on positional relationships, and is predicted by calculating the binding energies [75] . To better understand the functions of the lncRNAs and their corresponding target genes, NT, NR, KOG, KEGG, and SwissProt annotations were assigned to the assembled novel and known mRNAs using Blast [76] or Diamond [77] , Gene ontology (GO) annotations were assigned using Blast2GO [78] and NR, and InterPro annotations were assigned using InterProScan5 [79] . An FDR ≤ 0.01 was used to indicate significant enrichment.

Some lncRNAs can form miRNA precursors through intracellular shearing [80] . To identify lncRNAs as miRNA precursors during the early development of longan SE, the lncRNAs were aligned to miRBase [81] using Blast [77] (http://blast.ncbi.nlm.nih.gov/Blast.cgi). When looking for potential miRNA precursors, lncRNAs with miRNA precursor alignments greater than 90% were selected and considered precursor of lncRNAs. To predict lncRNAs as the target genes of miRNAs, the longan lncRNAs and miRNAs data were submitted to "psRNA-Target" (http://plantgrn.noble.org/psRNATarget/) [82] with expectation ≤5. lncRNAs were predicted as eTMs for miRNAs and target trapping was identified by TAPIR (http://bioinformatics.psb.ugent.be/webtools/tapir/) [83] , The Cytoscape_v3.5.1 software was used for network mapping of lncRNAs and related miRNAs and mRNAs.

The 20 lncRNAs with the most significant differences were screened in four length intervals (0-500 bp, 500-1000 bp, 1000-1500 bp and 1500-2000 bp) of significant lncRNAs from the EC to GE stage, and specific primers were designed according to the obtained gene sequences. cDNA synthesis of cDNA was performed according to SMART™ RACE cDNA Amplification Kit and TransScript miRNA First-Strand cDNA Synthesis SuperMix Instruction Manual. Ten-fold dilutions of cDNAs from longan somatic embryos at three stages were used as templates for qRT-PCR amplification on a Roche LightCycler 480 instrument (Roche Applied Science, Switzerland). The gene qRT-PCR was carried out using a SYBR premix Ex Taq™ kit (TaKaRa) with a 20 μL reaction system containing, 10 μL SYBR, 1 μL cDNA template, 0.8 μL each of forward and reverse primers and 7.4 μL of ddH 2 O. The procedure was as follows: 95°C predenaturation 30 s, 95°C denaturation 10 s, 60°C annealing 30 s, 72°C extension 15 s, 40 cycles. miRNA qPCR using TransStart Tip Green qPCR SuperMix, the reaction system was 20 μL, the application of Tip 10 μL, cDNA template 1 μL, specific and universal primers 0.8 μL, ddH2O 7.4 μL, procedures: 95°C predenaturation for 30 s and 40 cycles of 95°C denaturation for 10 s, 60°C annealing for 30 s, and 72°C extension for 15 s. miRNA qPCR was performed using TransStart Tip Green qPCR SuperMix in a 20 μL reaction system containing 10 μL Tip Green SuperMix, 1 μL cDNA template, 0.8 μL specific and universal primers, and 7.4 μL ddH2O. The procedure was: 95°C denaturation for 30 s and 40 cycles of 95°C denaturation for 10 s, 60°C annealing for 30 s, and 72°C extension for 10 s. The 2 −ΔΔCt method was used to calculate expression values. The primers used for qPCR are listed in Additional file 9.

Heat maps of lncRNAs were produced using the online website Omicshare (http://www.omicshare.com). The heat maps were generated by Z-core processing of qPCR and RNA-Seq expression, which was the expression of each gene minus the mean of the gene in all samples and divided by the standard deviation.

Overexpression (agomir) and expression-inhibiting (antagomir) vectors of Dlo-miR172a, Dlo-miR159a.1 and Dlo-miR398a were synthesized by GenePharma. The Lipofectamine™ 2000 Transfection Reagent was used as a transfection reagent to transfer overexpression and

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Thanks to all the research workers at the Institute of Horticultural Biotechnology for their contribution to our study. We thank Robbie Lewis, MSc, from Liwen Bianji, Edanz Group China (www.liwenbianji.cn/ac), for editing a draft of this manuscript. 

All data presented in this study are provided either in the manuscript or additional files.

expression-inhibiting carriers into longan calli [84] . The processing system was: 445 μL MS, 30 μL transfection agent and 25 μL carriers (overexpression or inhibition of expression). Dlo-miR172a, Dlo-miR159a.1 and Dlo-miR398a overexpression and inhibition of expression materials were obtained after 24 h dark culture.

Additional file 1: Authors' contributions ZXL and YLL designed and coordinated the research, and helped to draft the manuscript. YC participated in its design, carried out the experimental work and wrote the manuscript. XL helped to draft the manuscript. LYS, XC, STZ, ZHZ, and YKC prepared the materials. YLL, ZXL, and YC analysed the data. XXH, YLL and ZXL revised the paper. All authors read and approved the final version of the manuscript. All authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.Ethics approval and consent to participate Experimental materials provided by the Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University, Fuzhou, Fujian, China.

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The authors declare that they have no competing interests.

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