key: cord-0012617-0axe6cu2
authors: Nandakumar, Shyama; Grushko, Olga; Buttitta, Laura A
title: Polyploidy in the adult Drosophila brain
date: 2020-08-25
journal: nan
DOI: 10.7554/elife.54385
sha: 986f9b1742bffef83795a5fb9279f5f5d98f1d8a
doc_id: 12617
cord_uid: 0axe6cu2

Long-lived cells such as terminally differentiated postmitotic neurons and glia must cope with the accumulation of damage over the course of an animal’s lifespan. How long-lived cells deal with ageing-related damage is poorly understood. Here we show that polyploid cells accumulate in the adult fly brain and that polyploidy protects against DNA damage-induced cell death. Multiple types of neurons and glia that are diploid at eclosion, become polyploid in the adult Drosophila brain. The optic lobes exhibit the highest levels of polyploidy, associated with an elevated DNA damage response in this brain region. Inducing oxidative stress or exogenous DNA damage leads to an earlier onset of polyploidy, and polyploid cells in the adult brain are more resistant to DNA damage-induced cell death than diploid cells. Our results suggest polyploidy may serve a protective role for neurons and glia in adult Drosophila melanogaster brains.

Terminally differentiated postmitotic cells such as mature neurons and glia are long-lived and must cope with the accumulation of damage over the course of an animal's lifespan. The mechanisms used by such long-lived cells to deal with aging-related damage are poorly understood. The brain of the fruit fly Drosophila melanogaster is an ideal context to examine this since the fly has a relatively short lifespan and the adult fly brain is nearly entirely postmitotic with well understood development and excellent tools for genetic manipulations.

The adult central nervous system of Drosophila melanogaster comprises~110,000 cells, most of which are generated in the larval and early pupal stages of development from various progenitor cell types (Truman and Bate, 1988; White and Kankel, 1978) . By late metamorphosis, the Drosophila pupal brain is normally completely non-cycling and negative for markers of proliferation such as thymidine analog incorporation and mitotic markers (Awasaki et al., 2008; Pahl et al., 2019; Siegrist et al., 2010) .

In the adult, very little neurogenesis and gliogenesis are normally observed (Awasaki et al., 2008; Ito and Hotta, 1992; von Trotha et al., 2009) . A population of about 40 adult neural progenitors has been reported in the optic lobe and a population of glial progenitors has been reported in the central brain (Fernández-Hernández et al., 2013; Foo et al., 2017) . Upon damage or cell loss, hallmarks of cycling have been shown to be activated, although the overall level of proliferation in the adult brain remains very low (Crocker et al., 2020; Fernandez-Hernandez et al., 2019; Fernández-Hernández et al., 2013; Foo et al., 2017; Li et al., 2020) . Thus, the brain of the adult fly is thought to be almost entirely postmitotic with most cells in G0 with a diploid (2C) DNA content. One known exception to this are the cells that constitute the 'blood-brain barrier' of Drosophila.

The 'blood-brain barrier' in Drosophila is made up of specialised cells called the Sub-perineurial glia (SPGs). These cells are very few in number and achieve growth without cell division by employing variant cell cycles termed endocycles, that involve DNA replication without karyokinesis or cytokinesis, as well as endomitotic cycles that involve DNA replication and karyokinesis without cytokinesis (Unhavaithaya and Orr-Weaver, 2012; Von Stetina et al., 2018) . The SPGs undergo these variant cell cycles to increase their size rapidly to sustain the growth of the underlying brain during larval development. The polyploidization of these cells plays an important role in maintaining their epithelial barrier function, although it remains unclear whether these cells continue to endocycle or endomitose in the adult.

Polyploidy can also confer an increased biosynthetic capacity to cells and resistance to DNA damage induced cell death (Edgar and Orr-Weaver, 2001; Lee et al., 2009; Mehrotra et al., 2008; Zhang et al., 2014) . Several studies have noted neurons and glia in the adult fly brain with large nuclei (Robinow and White, 1991; Winberg et al., 1992) and in some cases neurons and glia of other insect species in the adult CNS are known to be polyploid (Nordlander and Edwards, 1969) . Rare instances of neuronal polyploidy have been reported in vertebrates under normal conditions (Morillo et al., 2010) and even in the CNS of mammals (Ló pez-Sánchez and Frade, 2013; Shai et al., 2015) .

Polyploidization is employed in response to tissue damage and helps maintain organ size (Cohen et al., 2018; Tamori and Deng, 2013; Losick et al., 2016; Losick et al., 2013) . Therefore, polyploidy may be a strategy to deal with damage accumulated with age in the brain, a tissue with very limited cell division potential. Here we show that polyploid cells accumulate in the adult fly brain and that this proportion of polyploidy increases as the animals approach middle-age. We show that multiple types of neurons and glia which are diploid at eclosion which become polyploid specifically in the adult brain. We have found that the optic lobes of the brain contribute to most of the observed polyploidy. We also observe increased DNA damage with age, and show that inducing oxidative stress and exogenous DNA damage can lead to increased levels of polyploidy. We find that polyploid cells in the adult brain are resistant to DNA damage-induced cell death and propose a potentially protective role for polyploidy in neurons and glia in adult Drosophila melanogaster brains.

Cell ploidy often scales with cell size and biosynthetic capacity (Edgar and Orr-Weaver, 2001; Orr-Weaver, 2015) . The brain is thought to be a notable exception to this rule, where the size of postmitotic diploid neurons and glia can be highly variable. We wondered whether alterations in ploidy during late development or early adulthood may contribute to the variability in neuronal and glial cell size in the mature Drosophila brain. We therefore developed a sensitive flow cytometry assay to measure DNA content in Drosophila pupal and adult brains. Briefly, this assay involves dissociating brains with a trypsin or collagenase based solution followed by quenching the dissociation and labeling DNA with DyeCycle Violet (Grushko and Buttitta, 2015) in the same tube, to avoid cell loss from washes. Samples are then immediately run live on a flow cytometer for analysis. We employed strict gating parameters to eliminate doublets (Figure 1-figure supplement 1; Ló pez-Sánchez et al., 2017b) . This assay is sensitive enough to measure DNA content from small subsets of cells (e.g. Mz19-GFP expressing neurons) from individual pupal or adult brains (Figure 1-figure supplement 1D). Using this approach we confirmed that under normal culturing conditions, cell proliferation and DNA replication ceases in the pupal brain after 24 hr into metamorphosis (24 hr APF) (Figure 1-figure supplement 1E), and that only the previously described mushroom body neuroblasts continue to replicate their DNA and divide in late pupa (Siegrist et al., 2010) . The brains of newly eclosed adult flies are 98-99% diploid and we, like others, only rarely observe EdU incorporation during the first week of adulthood in wild-type flies under normal conditions but not later in adulthood (Figure 1-figure supplement 1F; Fernández-Hernández et al., 2013; Foo et al., 2017; Kato et al., 2009; Siegrist et al., 2010; von Trotha et al., 2009) . We were therefore surprised to find a distinct population of cells with DNA content of 4C and up to >16C appearing in brains of aged animals of various genotypes under normal culture conditions (Figure 1-figure supplement  1G ).

We performed a systematic time-course to measure accumulation of polyploid cells in the adult brain in isogenic w 1118 male and female flies cultured under standard conditions (Linford et al., 2013) . We measured the percentage of polyploid cells in individual brains from the day of eclosion until 56 days (8 weeks) at weekly intervals. Polyploid cells appear as early as 7 days into adulthood, and the proportion of polyploidy continues to rise until animals are 21 days old ( Figure 1A ). This increase in polyploidy is only observed until week 3, after which the proportion of polyploid cells observed remains variable from animal to animal, but on average, does not increase. We observe similar patterns of polyploidy accumulation in males and females ( Figure 1A ). To ensure that the polyploidy we observe is not an artefact of one particular strain, we performed similar measurements across the lifespan in other commonly used lab 'wild-type' strains Canton-S ( Figure 1B) and Oregon-R ( Figure 1C) . Interestingly, Oregon-R flies show lower levels of polyploidy in the first two weeks than w 1118 and Canton-S suggesting that different genetic backgrounds may influence polyploidy in the brain. We also performed DNA content measurements of brains from the distantly related D.americana which diverged~50 million years ago and a more closely related species, D.mauritiana, which diverged~2 million years ago ( Figure 1C ). While both species show accumulation of polyploidy, it is interesting to note that they show differences in levels of polyploidy. We next measured changes in ploidy in the D. melanogaster adult brain over time. We pooled data from multiple animals and binned polyploid cells from w 1118 brains into two categories: cells with 4C (tetraploid) DNA content measured by flow cytometry and cells with >4C DNA contentthis includes 8C, 16C and even some 32 C cells ( Figure 1D ). The majority of the polyploid cells appear to be tetraploid, and the fraction of cells exhibiting >4C DNA content increases during the first week of adulthood, but remains relatively consistent with age.

We next asked whether polyploid cells are located in a specific region of the brain. We dissected the Drosophila central nervous system (CNS) into the central brain, optic lobes, and ventral nerve cord (VNC) and measured levels of polyploidy in each region from day of eclosion to 2 weeks into adulthood ( Figure 1E ). We found that while there is a low level of polyploidy in the central brain and VNC that increases with age, most of the polyploidy comes from the optic lobes. Strikingly, by 3 weeks, over 20% of the cells in the optic lobes can exhibit polyploidy.

Since the optic lobes contribute to most of the polyploidy observed, we wondered if this phenomenon may be dependent on light. Canton-S animals reared in complete darkness did not show difference in polyploidy compared to age-matched controls raised in regular 12 hr light/12 hr dark cycles ( 

To identify which cell types in the brain are becoming polyploid, we used the binary GAL4/UAS system to drive the expression of a nuclear-localised green or red fluorescent protein (nGRP or nRFP) with cell type-specific drivers. We then measured DNA content using Dye-Cycle Violet in the GFP or RFP-positive populations.

We first examined the SPGs, as previous work from the Orr-Weaver lab identified these to be highly polyploid (Unhavaithaya and Orr-Weaver, 2012; Von Stetina et al., 2018) . When we used the SPG driver moody-GAL4, we found that the SPGs are highly polyploid (Unhavaithaya and Orr-Weaver, 2012) , but contributed to less than 5% the polyploid cells observed in mature adult brains (Figure 2-figure supplement 1A,C). Another class of cells previously shown to be polyploid in some contexts are tracheal cells that carry oxygen to tissues (Zhou et al., 2016) . Using the tracheal driver breathless-GAL4, we found that in 10 day old adult brains, tracheal cells comprise less than 3% of all polyploid cells (Figure 2-figure supplement 1B,C). Thus, 90% of the polyploid cells we observe in the brain arise from cell types not previously known to become polyploid.

The adult fly brain is thought to be composed almost entirely of neurons (90% of total population) and glia (10% of total population). First, we asked if neurons become polyploid by using a pan-neuronal driver, nSyb-GAL4 to drive UAS-nGFP ( Figure 2A ). We found that indeed, by two weeks~5-6% of cells expressing nSyb-GAL4 show >2C DNA content. Similarly, we used the pan-glial driver Repo-GAL4 and found that by 2 weeks~6-7% of glia also become polyploid in the adult brain ( Figure 2B ). Neurons outnumber glial cells in the fly brain, and we find that the relative proportions of polyploid cells reflect the total ratio of neurons vs. glia in the adult brain ( Figure 2C ). We next asked whether specific types of neurons or glia show higher levels of polyploidy. We measured the proportion of polyploid vs diploid cells in various classes of neurons ( Figure 2D ) and glia ( Figure 2E ) in 7 day old optic lobes. Interestingly, we found that most differentiated cell types we assayed in the optic lobes show some level of polyploidy by one week of age. We conclude that polyploidy arises in multiple neuronal and glial types that are initially diploid upon eclosion and become polyploid after terminal differentiation and specifically during adulthood.

We reasoned that cells in the brain could become polyploid either by re-entering the cell cycle or by undergoing cell fusion (Alvarez-Dolado and Martínez-Losa, 2011; Giordano-Santini et al., 2016; Grendler et al., 2019; Losick et al., 2013; Schoenfelder et al., 2014; Shu et al., 2018; Starnes et al., 2016) . To examine whether cell fusion occurs, we used a genetic labeling tool called CoinFLP (Bosch et al., 2015) . The CoinFLP genetic cassette contains two overlapping but exclusive Flippase Recombination Target (FRT) sites flanking a stop cassette that can be 'flipped -out' using Source data 1. Source Data for Figure 2C . Source data 2. Source Data for Figure 2D . FRT mediated recombination to give rise to cells expressing either a LexGAD driver or a GAL4 driver, which can be used to drive expression of lexA op -GFP (green) and UAS-RFP (red). In animals heterozygous for CoinFLP, a diploid cell has only one copy of the transgenic cassette which can only be 'flipped' to give rise to a cell permanently labeled with either red or green fluorescent proteins, hence the name CoinFLP. If labeling is induced in the brain early during development before eclosion, cells become stochastically and permanently labeled with either red or green fluorescent proteins. If cells fuse in the ageing brain, up to ⅓ of cells undergoing fusion could fuse a red-labeled cell with a green cell and appear yellow. We used a FLP recombinase (flippase) under the control of the eyeless promoter (ey-FLP) to label most of the cells red or green in the optic lobes early in development ( Figure 3A -B') and did not observe any double labeled (yellow) cells in young adult brains or older brains. We also expressed flippase enzyme more broadly under the control of a heat-shock promoter (hs-FLP) and labeled cells using a nuclear GFP or RFP at larval L2-L3 stages ( Figure 3C ) and measured the number of double-labeled cells in the optic lobes at on the day of eclosion or after aging at 14 days post-eclosion. We never observed more than 10-12 cells per optic lobes exhibiting double-labeling under these 'early-FLP' conditions. These double-labeled cells under the larval hs-FLP conditions likely include the SPG cells which become polyploid early in larval development and do not express ey-FLP. We conclude that very little cell fusion occurs in the adult OL, even with age.

'Late-FLP' can label polyploid cells that arise from cell cycle reentry By using a modified labeling paradigm, we can also use CoinFLP to label polyploid cells in situ ( Figure 4A ). Previous work with CoinFLP has shown that inducing 'flipping' in cells that are already polyploid results in a fraction of double labeled yellow cells (Bosch et al., 2015) . We therefore reasoned that heterozygous CoinFLP brain cells that become polyploid by replicating their genome during adulthood will contain two or more copies of the CoinFLP transgene cassette. If we label cells by activating hs-FLP late in adulthood after polyploidy appears, some polyploid cells may 'flip' one copy green and one copy red, appearing yellow. When we induce an adult FLP at one day, before polyploidy occurs, we do not observe any double-labeled cells in the optic lobe ( Figure 4B ) but when we induce an adult FLP at 30 days post-eclosion, we observe several double labeled cells ( Figure 4B ') indicating that these cells have undergone genome replication and contain at least two heterozygous copies of the CoinFLP transgenic cassette. To quantify this, we used an adult 'late-FLP' to drive nuclear GFP and RFP, and we observe around 300 double-labeled cells per optic lobes in 14 day old brains ( Figure 4C ). The presence of double-labelled nuclei in aged optic lobes suggest cells become polyploid by cell cycle re-entry and endoreduplicating DNA.

We further confirmed that the double-labeled cells visualized by microscopy are polyploid by performing DAPI intensity quantification in high-magnification images ( . CoinFLP double-labeling confirmed several types of glia identifiable by location and shape to become polyploid, such as a subset of cortex glia of the outer ( Figure 4D ) and inner ( Figure 4E ) optic chiasm and astrocyte-like glia ( Figure 4F ) in the medulla of the OL.

To test whether polyploidy in the adult optic lobes is driven by cell cycle re-entry, we used celltype specific RNA-interference (RNAi) to modulate the DNA replication licensing factors cdc6 and Geminin in postmitotic neurons. Cdc6 is an essential factor for DNA replication licensing that promotes the recruitment of the MCM complex to load the DNA replication complex , while Geminin is a replication licensing inhibitor that sequesters DNA replication licensing factors to inhibit DNA re-replication (Lutzmann et al., 2006) . Using nSyb-GAL4, we expressed UAS-cdc6 RNAi in differentiated neurons which significantly reduced levels of polyploidy by 14d ( Figure 4G ) from~25% in control optic lobes to~14% on optic lobes expressing the RNAi. We next knocked down geminin and found that we increase levels of polyploidy in the optic lobes ( Figure 4G ). This suggests that a fraction of post-mitotic neurons reactivate DNA replication to become polyploid in the adult fly brain.

To investigate whether transcriptional changes that occur with age may be associated with cell cycle reactivation and polyploidy in the brain, we performed RNA sequencing on three parts of the CNS: optic lobes, central brain and VNC from male and female Canton-S animals at different time points: Figure 3 . Very few polyploid cells arise from cell fusion in the adult brain. (A) Schematic of 'early labeling' using CoinFLP to identify potential cell fusion events. Early CoinFLP labeling will label diploid cells either with GFP or RFP. Any double-labeled cells in an older, polyploid brain will be a result of cell fusion. Representative images of 0 day (B) and 30 day polyploid optic lobes showing no double-labeled cells under 'Early-FLP' conditions when labeled using ey-FLP and membrane GFP and RFP. (C) Quantification of double labeled cells using nuclear GFP and RFP observed per brain lobe in early 'FLP' condition at 14 days. p value=0.0428 significance calculated using unpaired t-test with Welch's correction. Early 'FLP' in (C) was induced at L2-early L3 stages using hs-FLP. Scale bars = 8.3 mm. 1 day, 2 days, 7 days and 21 days post-eclosion. To infer biological processes that are affected with age, gene ontology analysis was performed using GOrilla and redundant terms were filtered using reviGO. The most significant changes observed in the optic lobes at 21d compared to 2d are shown in Figure 5A ,B. Among the most significantly upregulated groups of genes are those associated with the cell cycle, DNA damage response and DNA damage repair. The enrichment of up-regulated genes associated with the DNA damage response was also observed in the optic lobes at 7 days (Figure 5-figure supplement 1), but the enrichment and fold-induction of specific genes is stronger at day 21 ( Figure 5A) . A gene expression signature associated with DNA damage is specific to the optic lobes. However, the most significantly downregulated GO terms in the optic lobes at 21d are shared with the central brain and VNC and include metabolism, transmembrane transport and cellular respiration-associated processes ( Figure 5-figure supplement 1) .

To examine whether DNA damage is higher in the OL, we performed immunostaining against the phosphorylated histone 2A variant (pH2AV) in 1d optic lobes and central brain and 21d optic lobes and central brain ( Figure 5C -E) from Canton-S male brains. Young brains show very low levels of pH2AV in both the optic lobes and central brain ( Figure 5C ,C',E) but older brains show higher levels of pH2AV in the optic lobes compared to the central brain ( Figure 5D ,D',E).

To further understand the DNA damage and cell cycle signatures observed with age, we looked at the change in expression of specific genes involved in the DNA damage response and the cell cycle ( Figure 5F ). Recent work has identified a specific transcriptional response to induced DNA damage in the head that involved a non-canonical role for tumor suppressor protein p53 (Kurtz et al., 2019) . This signature was termed head Radiation Induced p53-Dependent or hRIPD. In addition to genes such as FANCI, loki, rad50 and xrp1 which are involved in a canonical, ionising radiation-induced DNA damage response, we also find robust upregulation of hRIPD genes Ku80, Irbp, Cht8, CG3344 and CG4734 in our RNAseq data set at 7d and 21d in optic lobes. However, these genes are not as strongly upregulated in the aged central brain or VNC and p53 itself shows only a small increase in the optic lobes at 21d ( Figure 5F ). Consistent with cell cycle re-entry in a fraction of cells in the OL, upregulation of cell cycle genes such as myc, cyclin D, orc1 is observed specifically in the optic lobes and increases with age.

Work in other polyploid tissues in Drosophila has shown that polyploid cells in the salivary gland can tolerate high levels of DNA double-strand breaks and resist apoptosis caused by DNA damage (Hassel et al., 2014; Mehrotra et al., 2008; Qi and Calvi, 2016; Zhang et al., 2014) . This is possible because polyploid cells in tissues such as the salivary gland have intrinsically low levels of p53 protein and also suppress the expression of pro-apoptotic genes . It has also been shown in various tissues and organisms that DNA damage can induce polyploidization (Bretscher and Fox, 2016; Donovan and Corbo, 2012; Grendler et al., 2019) . Since we observe a modest upregulation of p53 as well as a p53-dependent gene expression signature in older optic lobes, we asked if the induction of polyploidy in neurons is p53 dependent. To address this, we overexpressed wildtype (p53 WT ) or a dominant-negative allele of p53 (p53 DN ) that is unable to bind to Figure 4 continued nuclear GFP and RFP observed per brain lobe in 'late-FLP' condition. Labeling was induced 24 hr prior to dissection for both 1d and 14d using hs-FLP. P value < 0.0001 significance calculated using unpaired t-test with Welch's correction. (D-F) Representative images showing cortex glia of the outer (D) and inner (E) optic chiasm as well as astrocyte-like (F) glial nuclei that can be identified as polyploid based on position and morphology using CoinFLP 'late-FLP' labeling method. Polyploid, double-labeled glia of each type are indicated with white arrows (G) Inhibition of DNA replication licensing factor cdc6 by RNAi in neurons using the driver nsyb-GAL4 results in lower levels of polyploidy (measured by flow cytometry) in male optic lobes compared to control (GAL4 driver alone). Knockdown of replication inhibitor geminin increases levels of polyploidy in 14 day old male optic lobes. Error bars show mean ± SEM, n = 3. (Two way anova with greenhouse geisser correction for unequal SDs followed by Holm-Sidak's multiple comparisons test p values: 0.1234 = ns;<0.0332 *;<0.0021 **;<0.0002 ***; ****<0.0001) Scale bars for D-F = 20 mm. The online version of this article includes the following source data and figure supplement(s) for figure 4:

Source data 1. Source Data for Figure 4C . Figure 5 continued on next page DNA and evoke a transcriptional response in neurons using the nSyb-GAL4 driver ( Figure 6A ). We did not see a significant difference in levels of polyploidy in 7 day old brains with overexpression of either WT or mutant p53, suggesting that accumulation of polyploidy in neurons is p53-independent. We also performed cell death measurement in the brain using flow cytometry. We calculated cell death by measuring proportions of cells incorporating either Propidium Iodide (PI) or Sytox-Green ( Figure 6-figure supplement 1) . We did not see a significant difference in the proportion of dead cells in overexpression of p53 WT or p53 DN conditions compared to control ( Figure 6 -figure supplement 1B) consistent with recent work suggesting a non-canonical, non-apoptotic role for p53 in the adult Drosophila brain (Kurtz et al., 2019) .

We next asked if exogenous stress can impact levels of polyploidy in the brain. Increased oxidative stress is commonly associated with ageing (Haddadi et al., 2014; Hussain et al., 2018; Pinto and Moraes, 2015) . We first treated flies with a low dose of paraquat (PQ) to mimic oxidative stress (Bonilla et al., 2006; Dudas and Arking, 1995; Hosamani and Muralidhara, 2013; Zou et al., 2000) . w 1118 flies treated with low dose of 2 mM PQ from eclosion show increased DNA damage as well as increased polyploidy at 7d À14d ( Figure 6B ,D) but not increased cell death (Figure 6-figure supplement 1) .

We next tested whether inducing DNA damage directly affects polyploidy. We treated flies with 900mJ of UV radiation by placing flies in a UV Stratalinker at 2 days post-eclosion (Grendler et al., 2019; Kang and Bashirullah, 2014) and observed significantly increased levels of polyploidy at day seven in UV-treated flies compared to mock-treated controls ( Figure 6C ). We measured cell death using propidium-iodide (PI) incorporation (Grushko and Buttitta, 2015) and observed an acute increase in cell death 16 hr post-exposure to UV ( Figure 6E ), but no difference in cell death 5 days post-exposure. This suggests that cell death precedes accumulation of polyploidy upon induction of exogenous DNA damage.

Polyploid cells in other tissues are known to sustain high levels of DNA damage as well as resist cell death . We and others do not observe reproducible caspase-dependent cell death in the adult brain beyond the first 5 days after eclosion (Foo et al., 2017) . We measured cell death and necrosis in individual w 1118 adult brains over a time-course using PI incorporation from day one post-eclosion until day 56 (Grushko and Buttitta, 2015) . We found that newly eclosed flies exhibit a low level of dead or dying cells but from day 7 to day 56, the brain shows a relatively steady level (~5%) of dead or dying cells ( Figure 6F ) although there is variability from animal to animal. Since dead cells are cleared in the brain (Kurant, 2011) , we expect this steady rate of cell death to result in a predictable rate of cell loss in the brain with age, which closely agrees with our total cell counts performed using flow cytometry ( Figure 6-figure supplement 1) .

We next examined whether the polyploid cells in aged brains are protected from cell death. Since the numbers of dead or dying cells measured in individual brains was very small, we pooled brains from 2 week old Canton-S males to obtain a measurement of ploidy in the PI positive cells by costaining with the DNA content dye DyeCycle Violet. We found that while~7% of the diploid cells incorporate PI, less than~2.5% of polyploid cells incorporate PI ( Figure 6G ), suggesting that polyploid cells are more resistant to cell death.

To examine whether polyploid cells are resistant to cell death upon external DNA damage, we aged animals to 21 days, a time point where the OL exhibits high levels of polyploidy. We then exposed these flies to 480mJ UV to induce DNA damage and measured the levels of cell death and polyploidy from 24 hr -5 days post exposure to UV. We observe high levels of PI incorporation ( Figure 6H ,I) at 24 hr post exposure, but normal levels by 48 hr, indicating an acute response of DNA damage induced cell death in the brain. Many diploid cells die in response to this dose of UV (~24.5%). In contrast, the polyploid cells show very low levels of PI incorporation (~3.1%, Figure 6H ), suggesting that the polyploid cells in older adult brains are also resistant to DNA damage induced cell death. We next examined whether the exposure to DNA damage also altered polyploidy, as we had observed in younger animals ( Figure 6C ). At 48 hr we observed, on average, a 4% increase in polyploidy for UV exposed animals. This early increase can be almost entirely attributed to the loss of the diploid cells that are PI positive at 24 hr post exposure (a loss of 24.5% of diploid cells increases the proportion of polyploid cells from 18.9% to 23%). When comparing 48 hr to 5 days post exposure, we see no significant increase in polyploidy, suggesting that after 3 weeks of age, animals lose the ability to further increase polyploidy in response to damage. This is in contrast to our experiment in young animals, using a low dose of paraquat to cause oxidative damage ( Figure 6B,D) where we see an earlier accumulation of polyploid cells without any obvious increase in cell death ( Figure 6-figure supplement 1) .

The work described in this study supports a model ( Figure 6K) where cells in the early adult fly brain undergo endoreplication and polyploidization in response to DNA damage and oxidative stress accumulated with age. Our data also suggest that polyploid cells are more resistant to cell death and may serve a beneficial or neuroprotective role in the ageing brain.

In this study we describe a surprising discovery, that diploid cells in the adult Drosophila brain can re-enter the cell cycle and become polyploid. We have identified several classes of neurons as well as glia that exhibit adult-onset polyploidy. We have also characterized which regions of the brain Figure 6 continued control (n = 3). Error bars are mean ± SEM, significance was calculated by performing unpaired t-test with Welch's correction for unequal SD. (D) Accumulation of polyploidy over a time course in w 1118 males on 2 mM PQ (dark green) compared to control w 1118 males (light green). Shapes show mean, bars show SEM. Significance was calculated using two way ANOVA with Greenhouse-geisser correction for unequal SDs, multiple comparisons with Holm-Sidak's test; 0.1234 = ns;<0.0332 *;<0.0021 **;<0.0002 ***. (E) Cell death measured by Propidium Iodide incorporation in animals treated with 960mJ UV at 16 hr post-exposure and 5 days post-exposure. Cell death precedes accumulation of polyploidy upon induced DNA damage. Significance was calculated using two way ANOVA with Greenhouse-geisser correction for unequal SDs, multiple comparisons with Holm-Sidak's test; 0.1234 = ns;<0.0332 *;<0.0021 **;<0.0002 ***; ****<0.0001. (F) PI incorporation shows percentage of dead/dying cells in individual brains, male and female, w 1118 at different ages post-eclosion. Significance was calculated using two way ANOVA with Greenhouse-geisser correction for unequal SDs, multiple comparisons with Holm-Sidak's test; 0.1234 = ns;<0.0332 *;<0.0021 **;<0.0002 ***; ****<0.0001 (G). Proportion of PI+ cells that are diploid (2C) and polyploid (>2C) in pooled 14 day old Canton-S male brains. (H-J) Animals were exposed to 480 mJ UV at 21 days and dissected 24 hr, 48 hr or 5d post exposure and cell death (H,I) and polyploidy (J) was measured by flow cytometry. (H) Proportion of PI+ cells that are diploid (2C) and polyploid (>2C) in pooled 21d w 1118 male OL 24 hr post-exposure to 480mJ UV. (K) Proposed Model. For (G-I) n = 3, Error bars are mean ± SEM, significance was calculated by performing Two way ANOVA, multiple comparisons with Holm-Sidak's test; 0.1234 = ns;<0.0332 *;<0.0021 **;<0.0002 ***; ****<0.0001. The online version of this article includes the following source data and figure supplement(s) for figure 6:

Source data 1. Source Data for Figure 6D . Source data 2. Source Data for Figure 6F . Source data 3. Source Data for Figure 6H . Source data 4. Source Data for Figure 6I . Source data 5. Source Data for Figure 6J . show increased polyploidy, and find that polyploidy is closely correlated with the expression of a DNA damage response signature. Other work has also shown that a small population of about 40 stem cells in the optic lobes of Drosophila respond to acute injury by generating adult-born neurons (Fernández-Hernández et al., 2013) . We considered the possibility that a fraction of cells with 4C DNA content may be in G2 and poised to undergo mitosis. We stained for G2 and mitotic cell cycle markers (phospho-histone H3 and Cyclin A) in over 100 adult brains at different ages and never observed a convincing G2 or mitotic event. However, we may have missed rare, transient cell cycle events that are captured by permanent lineage tracing approaches (Crocker et al., 2020; Fernández-Hernández et al., 2013) . Both our cell number counts and cell death measurements indicate a steady decline in cell number in the adult brain with age ( Figure 6-figure supplement 1) , and suggest that under normal ageing conditions mitoses are likely rare. Moreover, we observe hundreds to thousands of tetraploid or polyploid cells by FACS or CoinFLP, suggesting that only a very small proportion of tetraploid cells would be expected to be in G2. We suggest that multiple mechanisms are employed in this brain region to ensure proper function and tissue integrity with age.

Polyploidy in neurons has previously been reported in the mouse cerebral cortex (Ló pez-Sánchez et al., 2017a; Ló pez-Sánchez and Frade, 2013) and chick retinal ganglion cells (Morillo et al., 2010) . Whether purkinje cells in the mammalian cerebellum are polyploid has been a matter of considerable debate over the past several decades. (Brodskii et al., 1971; Del Monte, 2006; Kemp et al., 2012; Lapham, 1968; Lapham et al., 1971; Mares et al., 1973; Swartz and Bhatnagar, 1981) . Perhaps the most exaggerated examples of polyploidy are from the giant neurons in the terrestrial slug Limax (Yamagishi et al., 2011) and the sea slug Aplysia (Coggeshall et al., 1970) where giant neurons contain >100,000 copies of the diploid genome. However, in all these cases, polyploid neurons appear during development. Our study describes a novel phenomenon of adult onset and accumulation of polyploidy in the Drosophila brain under normal physiological ageing conditions.

What is the function of polyploidization in the brain?

We have shown that many cell types become polyploid in the adult brain ( Figure 2) . These cell types have distinct physiology and functions. How polyploidization affects the function of these various cell types is an exciting avenue for future research. Polyploidy can confer cell-type and context specific benefits in various tissues. In Drosophila, polyploid intestinal enterocytes (Miguel-Aliaga et al., 2018) , SPGs (Unhavaithaya and Orr-Weaver, 2012; Von Stetina et al., 2018) and cells in the wounded epithelium (Losick, 2016; Losick et al., 2013) undergo endoreduplication and do not undergo cytokinesis to maintain the integrity of the blood brain barrier and the cell-cell junctions in the epithelium respectively. One possibility is that polyploidy in neurons or glia may allow cells to compensate for cell loss while maintaining established cell-cell contacts (Unhavaithaya and Orr-Weaver, 2012) . The compound eye and optic lobes of Drosophila contain~750-800 ommatidial 'units' that form a highly organized and crystalline structure (Bates et al., 2019; Nériec and Desplan, 2016; Pecot et al., 2014) . Numerically and topographically matched cells in the medulla cortex of the optic lobes receive inputs from the lamina which in turn receives inputs from the retina (Bates et al., 2019; Pecot et al., 2014) . We observe polyploidization in multiple neuronal types found in the medulla, yet several cell types in the brain show a decline in number with age (Bates et al., 2019) . In neurons, polyploidy could play a role in helping cells increase their soma size and dendritic arbors (Morillo et al., 2010; Szaro and Tompkins, 1987) . It is possible that polyploidy allows neurons to form more presynaptic and postsynaptic connections to compensate for lost cells while maintaining the integrity of existing connections in the visual system.

Nurse cells in the egg chamber (Lilly and Spradling, 1996; Wattiaux and Tsien, 1971) , cells in the accessory gland (Box et al., 2019; Sitnik et al., 2016) , salivary gland (Edgar and Orr-Weaver, 2001 ) and fat body (Guarner et al., 2017) , on the other hand become polyploid to fulfill increased biosynthetic demands. In addition to an upregulation of DNA damage and cell cycle in the optic lobes, our RNAseq data suggest compromised metabolism with age in all parts of the brain. One of the main functions of glial cells is to provide metabolic support to neurons in the brain (Kremer et al., 2017; Schirmeier et al., 2016; Volkenhoff et al., 2015) . Polyploidization in astrocyte and cortex glial cells might also serve to increase their metabolic output and compensate for the reduced metabolic output in the ageing brain.

We observe higher levels of expression of DNA damage-associated genes in the optic lobes than in other parts of the brain ( Figure 5A ). We also see higher levels of DNA damage foci in the optic lobes than the central brain. We observe this signature even at 7 days in the OL, but it becomes stronger by 21 days (Figure 5-figure supplement 1) . This is consistent with other studies that report that signatures of ageing appear gradually over the course of an organism's lifespan and not abruptly at later chronological ages (Ben-Zvi et al., 2009; Labbadia and Morimoto, 2014; Shavlakadze et al., 2019) . We do not know whether the increased DNA damage signature we observe in the optic lobes is because the optic lobes intrinsically sustain higher levels of DNA damage or whether other parts of the brain are better equipped to resolve DNA lesions. We also see an upregulation of cell cycle-associated genes specifically in the optic lobes with age. The transcription of cell cycle genes and genes involved in the DNA damage response and repair are intimately coordinated and can be controlled by intersecting pathways. Herrup et al., 2013; Uxa et al., 2019) . Homology-directed repair of DNA lesions occurs in S and G2 phases of the cell cycle in actively dividing cells (Herrup and Yang, 2007) . In other phases of the cell cycle, and after cell cycle exit, cells have to rely on error-prone non-homologous end joining mediated repair. It is tempting to speculate that re-entering the cell cycle allows postmitotic cells to repair DNA damage better and survive.

We and others observe a steady decline in the number of cells in the adult Drosophila brain with age ( Figure 6 -figure supplement 1; Bates et al., 2019; Foo et al., 2017) . The continual loss of cells in the ageing brain may be analogous to wounding, which induces polyploidization or compensatory cellular hypertrophy in other Drosophila tissues (Bretscher and Fox, 2016; Cohen et al., 2018; Losick et al., 2013) , (Tamori and Deng, 2013) . We suggest neurons and glia in the adult brain may employ a similar strategy, to compensate for cell loss in a non-autonomous fashion. When we induce damage that does not increase cell death in young brains ( Figure 6B,D) we observe an earlier increase in polyploidy, suggesting that in younger animals polyploidy can be an adaptive response to damage. By contrast in older animals, we find that polyploidy can protect from acute cell loss. However, levels of subsequent polyploidy do not further increase in aged animals, suggesting there is a permissive window for damage-induced polyploidy during adulthood ( Figure 6 ). This may explain why levels of polyploidy plateau after 3-4 weeks of age in various strains (Figure 1 ). It will be interesting to further test the nature of this compensation for cell loss in early adulthood by performing genetic experiments to ablate specific cell types or sub-populations of cells.

Over the past two decades, several studies have reported an interesting correlation between neurodegeneration and cell cycle re-entry in neurons Frade and Ovejero-Benito, 2015; Herrup, 2012; Moh et al., 2011; Rimkus et al., 2008; Yang and Herrup, 2005) . Most of these observations are from post-mortem brains containing neurons expressing cell cycle genes or exhibiting hyperploidy (>2N DNA content). More hyperploidy is observed in brains of patients with preclinical Alzheimer's compared to age-matched controls, which has led to the hypothesis that cell cycle re-entry may precede cell death and neurodegeneration. Whether cell cycle re-entry is a cause or a consequence of neurodegeneration has been difficult to test, since both are associated with age and damage. Our data suggest that re-entry into the cell cycle may be a normal physiological response to the accumulation of damage in early adulthood and that it can serve a beneficial and protective function in neurons and glia. However, we do not know how polyploidy may impact neuronal and glial function and whether it may become detrimental over time. In geriatric animals (beyond 4 weeks) we observe increased variation in the levels of polyploidy and we note that a subset of animals also exhibit extreme levels of cell death ( Figure 6C ). It is possible that these animals represent a fraction of the aged population that exhibit neurodegeneration. Our single-animal assays will be essential to identify these outliers for further study. 

Flies were reared and aged in a protocol modified from Linford et al., 2013 . Ageing flies were collected soon after eclosion as virgin males and females and segregated into vials containing no more than 20 flies/vial. Ageing flies were flipped onto fresh Bloomington Cornmeal food every 5-7 days. A list of all fly stocks used in this study is supplied as a table in Supplementary file 2.

For pH2AV quantification, five non-overlapping Regions of Interest (ROIs) were chosen per brain region per brain. Average Intensity of pH2AV and DAPI per ROI were computed on individual channels using ImageJ. All brains were imaged at the same laser intensity and gain settings at different ages.

CoinFLP double-labeled cell counting was performed manually. Individual optic lobes were imaged at 100x magnification with 0.5 micron Z-sections. Quantification was performed by cropping 2-5 confocal Z-sections at a time, performing maximum intensity projections of each cropped image, and counting cells that showed DAPI, GFP and RFP signal overlap. Lamin staining was used to discern nuclear boundaries for DAPI Integrated Intensity measurements of 132 cells using FIJI. DAPI intensity was normalized to diploid cells (2N) measured on the same slide.

CoinFLP labeling was induced with heat shock induction. Flies were placed in plastic vials and completely submerged in 37˚C water bath for 15 min. For 'early-FLP', flies were moved back to 23˚C and dissected at day 1 or day 10. For 'late-FLP', heat shock induction was performed 24 hr prior to dissection. All incubations and culturing except heat shock was performed at 23˚C. We noted that the frequency of CoinFLP flipping resulted in a ratio of LexA:GAL4 expressing cells that is between 4:1 and 4.6:1 (Bosch et al., 2015) . We calculated the expected number of double labeled cells for 'late-FLP' in Figure 4 and Figure 4 -figure supplement 2 as follows: If flipping is complete (100% of cells flip), we would expect 80% of diploid cells to label red and~20% to label green. Only 4% of all polyploid cells will label green/green (probability of green is 0.2 therefore 0.2* 0.2 = 0.04*100), 64% red/red (probability of red is 0.8 thus, 0.8*0.8 = 0.64*100) and 32% will label green/red or red/ green and appear yellow or 'double-labeled'. If we assume that about 20% of cells in the optic lobes are tetraploid (20% of~30,000 = 6,000 cells), we can expect 1,920 cells (32% of 6,000) to label yellow per optic lobe under 100% flipping conditions. If we flip~50% of cells, we expect about 900 yellow cells per optic lobe. In our measurements the amount of flipping was variable from animal to animal and we estimate that in our samples with the lowest flipping we flip about ⅓ of cells and with our strongest flipping we label about ¾ cells.

Fly brains were dissected in PBS and transferred to 1.5 mL microcentrifuge tube caps containing 100 uL of solution containing 9:1 Trypsin-EDTA: 10XPBS with 1 mL Dyecycle Violet and/or 1.12 mL PI or 1 mL Sytox green. Brains were incubated for 20 min in the microcentrifuge tube caps, triturated using low retention p200 pipette tips for 60 s then transferred into the microcentrifuge tubes containing 400 mL of the trypsin-EDTA solution with dyes and capped, and incubated further for 45 min at room temperature without agitation. After incubation, each sample was diluted with 500 mL 1XPBS and gently vortexed at speed eight before being loaded onto Attune or Attune NxT flow cytometer for flow cytometry analysis. The Attune had a laser configuration of a violet laser (VL,405nm) with six bandpass (BP) filters and a blue laser (BL,488nm) with three bandpass filters. The Attune NxT is configured with VL (6 BP filters), BL with 2 BP filters, a yellow laser (YL, 561 nm) with 3 BP filters and a red laser (RL, 637 nm) with 3 BP filters. The detection of DyeCycle Violet was performed using VL1 (Emission filter 450/40), GFP and Sytox Green using BL1 (Emission filter 530/30), RFP and PI using BL2 (Emission filter 574/24) on the Attune and YL1 (585/16) on the Attune NxT. A flow rate of 100 to 500 ml/second was used for sample acquisition and a minimum of 20,0000 events gated as 'non doublets' (Figure 1-figure supplement 1) were acquired per sample. Gating Strategy is graphed in Figure 1 -figure supplement 1. Briefly, all cells were plotted on forward vs side scatter (FSC vs. SSC), gated to eliminate debris. Subsequently, 'non-debris' were plotted on VL1(DNA) vs FSC and gated to eliminate unstained events. A third gate was applied plotting VL1(DNA)-H vs VL1(DNA)-A (voltage pulse area vs.height) to eliminate doublets. All events in gate three were further subjected to GFP/DNA/PI content analysis.

10 CNSs from Canton-S females and males raised at 25˚C on Cornmeal/Dextrose food under normal 12 h L/D cycles at ZT = 2, were dissected into optic lobes, VNC and central brain at the indicated ages with three biological replicates for each sex, age and region (72 samples total). Tissues were directly dissolved into TRIZOL-LS. (Invitrogen) and RNA was prepared as directed by the manufacturer. Total RNA (2-5 mg) was provided to the University of Michigan Sequencing Core for polyA selection and unstranded mRNA library preparation for the Illumina HiSeq4000 platform.

RNAseq analysis was performed at the U.Michigan Bioinformatics Core using the following pipeline:

1.Read files from the Sequencing Core were concatenated into single fastq files for each sample. 2. Quality of the raw reads data for each sample was checked using FastQC(version v0.11.7). 3. Adaptors and poor quality bases were trimmed from reads using bbduk from the BBTools suite (v37.90).4. Quality processed reads were aligned to the Ensembl Dm6 genome using STAR (v2.6.1a) with quantMode GeneCounts flag option set to produce gene level counts. MultiQC (v1.6a0) was run to summarize QC information for raw reads, QC processed reads, alignment, and gene count information. Differential expression analyses were carried out using DESeq2 (v1.14.1). Data were pre-filtered to remove genes with 0 counts in all samples. Normalization and differential expression was performed with DESeq2, using a negative binomial generalized linear model. Plots were generated using variations or alternative representations of native DESeq2 plotting functions, ggplot2, plotly, and other packages within the R environment.

Genes called as at least 2-fold differentially expressed between day 2 and day 21 were examined for enriched GO terms using target and background unranked lists in GOrilla and redundant GO terms were filtered using ReviGO. GO term Enrichment is presented as the -log10 of the p-value with a cutoff at p-values higher than 10^À3. The full dataset has been uploaded to GEO and can be found using the accession number: GSE153165.

Sequencing data have been deposited in GEO under accession code GSE153165.

The following dataset was generated: 

Cell fusion and tissue regeneration

Organization and postembryonic development of glial cells in the adult central brain of Drosophila

Neuronal cell types in the fly: single-cell anatomy meets singlecell genomics

Collapse of proteostasis represents an early molecular event in Caenorhabditis elegans aging

Paraquat-induced oxidative stress in Drosophila Melanogaster: effects of melatonin, glutathione, serotonin, minocycline, lipoic acid and ascorbic acid

CoinFLP: a system for efficient mosaic screening and for visualizing clonal boundaries in Drosophila

Endocycles support tissue growth and regeneration of the adultDrosophilaaccessory gland

Proliferation of Double-Strand Break-Resistant polyploid cells requires Drosophila FANCD2

Multiple increase of DNA content in purkinje cells in the ontogeny of the rat

DNA damage and cell cycle events implicate cerebellar dentate nucleus neurons as targets of Alzheimer's disease

A cytophotometric analysis of the DNA in the nucleus of the giant cell, R-2, in Aplysia

Fizzy-Related dictates A cell cycle switch during organ repair and tissue growth responses in the Drosophila hindgut

Regeneration in the adult Drosophila brain

The puzzle of ploidy of purkinje neurons

Retinal horizontal cells lacking Rb1 sustain persistent DNA damage and survive as polyploid giant cells

A coordinate upregulation of antioxidant gene activities is associated with the delayed onset of senescence in a Long-Lived strain of Drosophila

Endoreplication cell cycles

Adult neurogenesis in Drosophila

Generation of mechanosensory neurons in adult Drosophila

miR-31 mutants reveal continuous glial homeostasis in the adult Drosophila brain

Neuronal cell cycle: the neuron itself and its circumstances

Cell-cell fusion in the nervous system: alternative mechanisms of development, injury, and repair

Wound-induced polyploidization is driven by myc and supports tissue repair in the presence of DNA damage

A sensitive assay for hyperploidy and cell death in the Drosophila brain using the attune Acoustic Focusing Cytometer

E2F/DP prevents Cell-Cycle progression in endocycling fat body cells by suppressing dATM expression

Brain aging, memory impairment and oxidative stress: a study in Drosophila Melanogaster

Induction of endocycles represses apoptosis independently of differentiation and predisposes cells to genome instability

The circadian clock of fruit flies is blind after elimination of all known photoreceptors

The contributions of unscheduled neuronal cell cycle events to the death of neurons in alzheimer s disease

The role of ATM and DNA damage in neurons: upstream and downstream connections

Cell cycle regulation in the postmitotic neuron: oxymoron or new biology

Acute exposure of Drosophila melanogaster to paraquat causes oxidative stress and mitochondrial dysfunction

Inhibition of oxidative stress in cholinergic projection neurons fully rescues aging-associated olfactory circuit degeneration in Drosophila

Proliferation pattern of postembryonic neuroblasts in the brain of Drosophila melanogaster dev

Multiple functions for Mcm2-7 ATPase motifs during replication initiation

A steroid-controlled global switch in sensitivity to apoptosis during Drosophila development

Neuronal programmed cell death induces glial cell division in the adult Drosophila brain

Purkinje cell fusion and binucleate heterokaryon formation in multiple sclerosis cerebellum

The Glia of the adult Drosophila nervous system

Keeping the CNS clear: glial phagocytic functions in Drosophila

Drosophila p53 directs nonapoptotic programs in postmitotic tissue

Proteostasis and longevity: when does aging really begin? F1000Prime Reports 6:7

Tetraploid DNA content of purkinje neurons of human cerebellar cortex

Postnatal development of tetraploid DNA content in the purkinje neuron of the rat: an aspect of cellular differentiation

Endoreplication: polyploidy with purpose

A Toll-receptor map underlies structural brain plasticity

The Drosophila endocycle is controlled by cyclin E and lacks a checkpoint ensuring S-phase completion

Measurement of lifespan in Drosophila melanogaster

Neuronal tetraploidization in the cerebral cortex correlates with reduced cognition in mice and precedes and recapitulates alzheimer's-associated neuropathology

Flow cytometric quantification, isolation, and subsequent epigenetic analysis of tetraploid neurons

Genetic evidence for p75NTR-dependent tetraploidy in cortical projection neurons from adult mice

Polyploidization and cell fusion contribute to wound healing in the adult Drosophila epithelium

Wound-Induced polyploidy is required for tissue repair

Wound-Induced polyploidization: regulation by hippo and JNK signaling and conservation in mammals

A Cdt1-geminin complex licenses chromatin for DNA replication and prevents rereplication during S phase in xenopus

A cytochemical and autoradiographic study of nuclear DNA in mouse purkinje cells

Endocycling cells do not apoptose in response to DNA rereplication genotoxic stress

Anatomy and physiology of the digestive tract of Drosophila melanogaster

Cell cycle deregulation in the neurons of Alzheimer's disease. Results and Problems in Cell Differentiation

Somatic tetraploidy in specific chick retinal ganglion cells induced by nerve growth factor

From the eye to the brain: development of the Drosophila visual system

Postembryonic brain development in the monarch butterfly,Danaus Plexippus plexippus, L. : I. cellular events during brain morphogenesis

When bigger is better: the role of polyploidy in organogenesis

E93 integrates neuroblast intrinsic state with developmental time to terminate MB neurogenesis via autophagy

Sequential axon-derived signals couple target survival and layer specificity in the Drosophila visual system

Mechanisms linking mtDNA damage and aging

Different cell cycle modifications repress apoptosis at different steps independent of developmental signaling in Drosophila mol

Mutations in string/ CDC25 inhibit cell cycle re-entry and neurodegeneration in a Drosophila model of ataxia telangiectasia

Characterization and spatial distribution of the ELAV protein during Drosophila Melanogaster development

Axon ensheathment and metabolic supply by glial cells in Drosophila

Indispensable premitotic endocycles promote aneuploidy in the Drosophila rectum

Physiology of layer 5 pyramidal neurons in mouse primary visual cortex: coincidence detection through bursting

Age-Related gene expression signature in rats demonstrate early, late, and linear transcriptional changes from multiple tissues

Endoreplication: the good, the bad, and the ugly

Inactivation of both foxo and reaper promotes long-term adult neurogenesis in Drosophila curr

The female Post-Mating response requires genes expressed in the secondary cells of the male accessory gland in Drosophila Melanogaster

Multi-nucleate retinal pigment epithelium cells of the human macula exhibit a characteristic and highly specific distribution

Are CNS neurons polyploid? A critical analysis based upon cytophotometric study of the DNA content of cerebellar and olfactory bulbar neurons of the bat

Effect of tetraploidy on dendritic branching in neurons and glial cells of the frog, xenopus laevis

Tissue repair through cell competition and compensatory cellular hypertrophy in postmitotic epithelia

Spatial and temporal patterns of neurogenesis in the central nervous system of Drosophila melanogaster dev

Polyploidization of Glia in neural development links tissue growth to blood-brain barrier integrity

DREAM and RB cooperate to induce gene repression and cell-cycle arrest in response to p53 activation

Glial glycolysis is essential for neuronal survival in Drosophila

Variant cell cycles regulated by notch signaling control cell size and ensure a functional blood-brain barrier

Cell proliferation in the Drosophila adult brain revealed by clonal analysis and bromodeoxyuridine labelling

Age effects on the variation of RNA synthesis in the nurse cells in Drosophila exp

Patterns of cell division and cell movement in the formation of the imaginal nervous system in Drosophila melanogaster

Generation and early differentiation of glial cells in the first optic ganglion of Drosophila melanogaster

DNA endoreplication in the brain neurons during body growth of an adult slug

Loss of neuronal cell cycle control in ataxia-telangiectasia: a unified disease mechanism

Low levels of p53 protein and chromatin silencing of p53 target genes repress apoptosis in Drosophila endocycling cells

Failure to burrow and tunnel reveals roles for Jim Lovell in the growth and endoreplication of the Drosophila Larval Tracheae

Genome-wide study of aging and oxidative stress response in Drosophila Melanogaster

We would like to thank members of the Buttitta and Cheng-Yu Lee labs for helpful discussions and suggestions. We also thank Yiqin Ma, Kerry Flegel, Chelsea Yu, Emily Lerner, Ashley Francis, Andrew White and Emily Rozich for help with experiments. We would also like to thank the Neuroscience and Drosophila research communities at UM for their support for providing fly stocks, particularly the labs of Cheng-Yu Lee, Monica Dus, Catherine Collins, Josie Clowney, Trisha Wittkopp, Scott Pletcher and Orie Shafer. We acknowledge support from the Bioinformatics Core and Chris Sifuentes of the University of Michigan Medical School's Biomedical Research Core Facilities. This study was funded by NIH R21 AG047931, NIH R01 GM127367, ACS Scholar Award RSG-15-161-01-DDC. SN was supported in part by the Barbour Scholarship (University of Michigan). 

Source or reference Identifiers

Genetic reagent (D. melanogaster) w 1118 ;+;GMR-30B06-GAL4