Monovalent and unpoised status of most genes in undifferentiated cell-enriched Drosophila testis.

Monovalent and unpoised status of most genes in undifferentiated cell-enriched Drosophila testis.
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DOI:
10.1186/gb-2010-11-4-r42
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发表时间:
2010
期刊:
影响因子:
12.3
通讯作者:
Chen X
Chen X
中科院分区:
生物学1区
文献类型:
--
作者:
Gan Q;Schones DE;Ho Eun S;Wei G;Cui K;Zhao K;Chen X

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In undifferentiated Drosophila cells, differentiation-associated genes have monovalent, not bivalent histone modifications, in contrast to differentiation-associated genes in stem cells. Increasing evidence demonstrates that stem cells maintain their identities by a unique transcription network and chromatin structure. Opposing epigenetic modifications H3K27me3 and H3K4me3 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 H3K27me3 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.
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发表时间: 2007-07-13
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影响因子: 64.5
作者:
Guenther, Matthew G.;Levine, Stuart S.;Young, Richard A.
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期刊: DEVELOPMENTAL CELL
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DOI: 10.1016/j.stem.2008.11.011
发表时间: 2009-01-09
期刊: Cell stem cell
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发表时间: 2009-05-01
影响因子: 4
作者:
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