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Spp1,Set1 复合物的一个成员,通过将组蛋白 H3K4 甲基化位点连接到染色体轴上,促进了启动子中的减数分裂 DSB 形成。

Spp1, a member of the Set1 Complex, promotes meiotic DSB formation in promoters by tethering histone H3K4 methylation sites to chromosome axes.

机构信息

Institut Curie, Centre de Recherche, 75248 Paris, France.

出版信息

Mol Cell. 2013 Jan 10;49(1):43-54. doi: 10.1016/j.molcel.2012.11.008. Epub 2012 Dec 13.

Abstract

Meiotic chromosomes are organized into arrays of loops that are anchored to the chromosome axis structure. Programmed DNA double-strand breaks (DSBs) that initiate meiotic recombination, catalyzed by Spo11 and accessory DSB proteins, form in loop sequences in promoters, whereas the DSB proteins are located on chromosome axes. Mechanisms bridging these two chromosomal regions for DSB formation have remained elusive. Here we show that Spp1, a conserved member of the histone H3K4 methyltransferase Set1 complex, is required for normal levels of DSB formation and is associated with chromosome axes during meiosis, where it physically interacts with the Mer2 DSB protein. The PHD finger module of Spp1, which reads H3K4 methylation close to promoters, promotes DSB formation by tethering these regions to chromosome axes and activating cleavage by the DSB proteins. This paper provides the molecular mechanism linking DSB sequences to chromosome axes and explains why H3K4 methylation is important for meiotic recombination.

摘要

减数分裂染色体组织成环阵列,这些环阵列锚定在染色体轴结构上。由 Spo11 和辅助双链断裂 (DSB) 蛋白催化的、启动子中形成的、引发减数分裂重组的有丝分裂 DSB,而 DSB 蛋白位于染色体轴上。为了形成 DSB,将这两个染色体区域连接起来的机制仍然难以捉摸。在这里,我们表明 Spp1(Set1 复合物中保守的组蛋白 H3K4 甲基转移酶的成员)对于正常水平的 DSB 形成是必需的,并且在减数分裂期间与染色体轴相关,在那里它与 Mer2 DSB 蛋白发生物理相互作用。Spp1 的 PHD 指模模块可以读取靠近启动子的 H3K4 甲基化,通过将这些区域束缚在染色体轴上并激活 DSB 蛋白的切割,从而促进 DSB 的形成。本文提供了将 DSB 序列与染色体轴连接起来的分子机制,并解释了为什么 H3K4 甲基化对减数分裂重组很重要。

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