Meta-analysis reveals that genes regulated by the Y chromosome in Drosophila melanogaster are preferentially localized to repressive chromatin.

Meta-analysis reveals that genes regulated by the Y chromosome in Drosophila melanogaster are preferentially localized to repressive chromatin.
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DOI:
10.1093/gbe/evt005
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发表时间:
2013
影响因子:
3.3
通讯作者:
Hartl DL
Hartl DL
中科院分区:
生物学2区
文献类型:
--
作者:
Sackton TB;Hartl DL

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果蝇Y染色体是一条退化的异染色质染色体,几乎没有功能基因。尽管如此,D.黑腹果蝇对X连锁和常染色体基因的调节具有实质性的反式作用。然而,目前尚不清楚这些基因是否只是代表基因组的随机子集,或者特定的功能特性是否与Y连锁变异的调控易感性相关。在这里,我们提出了一个荟萃分析四个先前发表的微阵列研究Y连锁调控变异(YRV)在D。黑腹菌我们表明,YRV基因是远远从基因组的随机子集:他们更有可能是在抑制染色质的背景下,表达组织特异性,并在不同物种内和之间的表达比非YRV基因。此外,YRV基因比非YRV基因更可能与核纤层相关联,并且通常更可能在核中彼此靠近(尽管不是沿沿着)。综上所述,这些结果表明,Y染色体上的变异在改变基因组在染色质区室中的分布方式中起作用,无论是通过DNA结合蛋白的分布变化,还是通过细胞核中基因组空间排列的变化。
The Drosophila Y chromosome is a degenerated, heterochromatic chromosome with few functional genes. Despite this, natural variation on the Y chromosome in D. melanogaster has substantial trans-acting effects on the regulation of X-linked and autosomal genes. It is not clear, however, whether these genes simply represent a random subset of the genome or whether specific functional properties are associated with susceptibility to regulation by Y-linked variation. Here, we present a meta-analysis of four previously published microarray studies of Y-linked regulatory variation (YRV) in D. melanogaster. We show that YRV genes are far from a random subset of the genome: They are more likely to be in repressive chromatin contexts, be expressed tissue specifically, and vary in expression within and between species than non-YRV genes. Furthermore, YRV genes are more likely to be associated with the nuclear lamina than non-YRV genes and are generally more likely to be close to each other in the nucleus (although not along chromosomes). Taken together, these results suggest that variation on the Y chromosome plays a role in modifying how the genome is distributed across chromatin compartments, either via changes in the distribution of DNA-binding proteins or via changes in the spatial arrangement of the genome in the nucleus.
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期刊: GENETICS
影响因子: 3.3
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影响因子: 11.1
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