A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

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Citation Gan, Q., Schones, D.E., Ho Eun, S., Wei, G., Cui, K., Zhao, K., Chen, X. (2010). Monovalent and unpoised status of most genes in undifferentiated cell-enriched Drosophila testis.  Genome Biol. 11(4): R42. (Export to RIS)
FlyBase ID FBrf0211027
Publication Type Research paper
PubMed ID 20398323
PubMed Abstract Increasing evidence demonstrates that stem cells maintain their identities by a unique transcription network and chromatin structure. Opposing epigenetic modifications H3K27 me3 and H3K4 me3 have been proposed to label differentiation-associated genes in stem cells, progenitor and precursor cells. In addition, many differentiation-associated genes are maintained at a poised status by recruitment of the initiative RNA Polymerase II (Pol II) at their promoter regions, in preparation for lineage-specific expression upon differentiation. Previous studies have been performed using cultured mammalian embryonic stem cells. To a lesser extent, chromatin structure has been delineated in other model organisms, such as Drosophila, to open new avenues for genetic analyses.Here we use testes isolated from a Drosophila bag of marbles mutant strain, from which germ cells are in their undifferentiated status. We use these testes to study the endogenous chromatin structure of undifferentiated cells using ChIP-seq. We integrate the ChIP-seq with RNA-seq data, which measures the digital transcriptome. Our genome-wide analyses indicate that most differentiation-associated genes in undifferentiated cells lack an active chromatin mark and initiative Pol II; instead, they are associated with either the repressive H3K27 me3 mark or no detectable mark.Our results reveal that most of the differentiation-associated genes in undifferentiated-cell-enriched Drosophila testes are associated with monovalent but not bivalent modifications, a chromatin signature that is distinct from the data reported in mammalian stem or precursor cells, which may reflect cell type specificity, species specificity, or both.
DOI 10.1186/gb-2010-11-4-r42
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Language of Publication English
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Publication Type Journal
Abbreviation Genome Biol.
Title Genome Biology
Publication Year 2000-
ISBN/ISSN 1465-6906
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