| Literature DB >> 26700685 |
Ching-Po Yang1, Chi-Cheng Fu2, Ken Sugino1, Zhiyong Liu1, Qingzhong Ren1, Ling-Yu Liu1, Xiaohao Yao1, Luke P Lee3, Tzumin Lee4.
Abstract
A brain consists of numerous distinct neurons arising from a limited number of progenitors, called neuroblasts in Drosophila. Each neuroblast produces a specific neuronal lineage. To unravel the transcriptional networks that underlie the development of distinct neuroblast lineages, we marked and isolated lineage-specific neuroblasts for RNA sequencing. We labeled particular neuroblasts throughout neurogenesis by activating a conditional neuroblast driver in specific lineages using various intersection strategies. The targeted neuroblasts were efficiently recovered using a custom-built device for robotic single-cell picking. Transcriptome analysis of mushroom body, antennal lobe and type II neuroblasts compared with non-selective neuroblasts, neurons and glia revealed a rich repertoire of transcription factors expressed among neuroblasts in diverse patterns. Besides transcription factors that are likely to be pan-neuroblast, many transcription factors exist that are selectively enriched or repressed in certain neuroblasts. The unique combinations of transcription factors present in different neuroblasts may govern the diverse lineage-specific neuron fates.Entities:
Keywords: Antennal lobe; Mushroom body; Neural stem cell; RNA-seq; Transcription factor; Type II neuroblast
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Year: 2015 PMID: 26700685 PMCID: PMC4760311 DOI: 10.1242/dev.129163
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868