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组蛋白乙酰化控制失活 X 染色体复制动力学。

Histone acetylation controls the inactive X chromosome replication dynamics.

机构信息

Department of Biology, Technische Universität Darmstadt, Darmstadt 64287, Germany.

出版信息

Nat Commun. 2011;2:222. doi: 10.1038/ncomms1218.

Abstract

In mammals, dosage compensation between male and female cells is achieved by inactivating one female X chromosome (Xi). Late replication of Xi was proposed to be involved in the maintenance of its silenced state. Here, we show a highly synchronous replication of the Xi within 1 to 2 h during early-mid S-phase by following DNA replication in living mammalian cells with green fluorescent protein-tagged replication proteins. The Xi was replicated before or concomitant with perinuclear or perinucleolar facultative heterochromatin and before constitutive heterochromatin. Ectopic expression of the X-inactive-specific transcript (Xist) gene from an autosome imposed the same synchronous replication pattern. We used mutations and chemical inhibition affecting different epigenetic marks as well as inducible Xist expression and we demonstrate that histone hypoacetylation has a key role in controlling Xi replication. The epigenetically controlled, highly coordinated replication of the Xi is reminiscent of embryonic genome replication in flies and frogs before genome activation and might be a common feature of transcriptionally silent chromatin.

摘要

在哺乳动物中,雄性和雌性细胞之间的剂量补偿是通过使一条雌性 X 染色体(Xi)失活来实现的。有人提出,Xi 的晚期复制参与了其沉默状态的维持。在这里,我们通过用绿色荧光蛋白标记的复制蛋白在活的哺乳动物细胞中追踪 DNA 复制,显示 Xi 在早-中期 S 期内 1 到 2 小时内高度同步复制。Xi 在核周或核周异染色质和组成型异染色质之前复制,或与它们同时复制。从常染色体异位表达 X 失活特异性转录物(Xist)基因会产生相同的同步复制模式。我们使用影响不同表观遗传标记的突变和化学抑制以及诱导性 Xist 表达,并证明组蛋白低乙酰化在控制 Xi 复制中起着关键作用。Xi 的这种受表观遗传控制的高度协调复制类似于果蝇和青蛙在基因组激活前的胚胎基因组复制,可能是转录沉默染色质的共同特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74a2/3072080/7ce3b2c088d2/ncomms1218-f1.jpg

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