A gene expression atlas of embryonic neurogenesis in Drosophila reveals complex spatiotemporal regulation of lncRNAs.
Alexandra L McCorkindalePhilipp WahleSascha WernerIrwin JungreisPeter MenzelChinmay J ShuklaRúben Lopes Pereira AbreuRafael A IrizarryIrmtraud M MeyerManolis KellisRobert P ZinzenPublished in: Development (Cambridge, England) (2019)
Cell type specification during early nervous system development in Drosophila melanogaster requires precise regulation of gene expression in time and space. Resolving the programs driving neurogenesis has been a major challenge owing to the complexity and rapidity with which distinct cell populations arise. To resolve the cell type-specific gene expression dynamics in early nervous system development, we have sequenced the transcriptomes of purified neurogenic cell types across consecutive time points covering crucial events in neurogenesis. The resulting gene expression atlas comprises a detailed resource of global transcriptome dynamics that permits systematic analysis of how cells in the nervous system acquire distinct fates. We resolve known gene expression dynamics and uncover novel expression signatures for hundreds of genes among diverse neurogenic cell types, most of which remain unstudied. We also identified a set of conserved long noncoding RNAs (lncRNAs) that are regulated in a tissue-specific manner and exhibit spatiotemporal expression during neurogenesis with exquisite specificity. lncRNA expression is highly dynamic and demarcates specific subpopulations within neurogenic cell types. Our spatiotemporal transcriptome atlas provides a comprehensive resource for investigating the function of coding genes and noncoding RNAs during crucial stages of early neurogenesis.
Keyphrases
- gene expression
- single cell
- dna methylation
- rna seq
- poor prognosis
- genome wide
- spinal cord injury
- cell therapy
- cerebral ischemia
- neural stem cells
- drosophila melanogaster
- long non coding rna
- public health
- binding protein
- stem cells
- brain injury
- induced apoptosis
- subarachnoid hemorrhage
- bone marrow
- cell death
- oxidative stress
- long noncoding rna
- genome wide analysis
- bioinformatics analysis