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一个新的减数分裂特异性黏合蛋白复合物,涉及黏合蛋白同源配对的密码。

A new meiosis-specific cohesin complex implicated in the cohesin code for homologous pairing.

机构信息

Laboratory of Chromosome Dynamics, Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Tokyo 113-0032, Japan.

出版信息

EMBO Rep. 2011 Mar;12(3):267-75. doi: 10.1038/embor.2011.2. Epub 2011 Jan 28.

Abstract

We identify a new mammalian cohesin subunit, RAD21-like protein (RAD21L), with sequence similarity to RAD21 and REC8. RAD21L localizes along axial elements in early meiotic prophase, in a manner that is spatiotemporally different to either REC8 or RAD21. Remarkably, RAD21L and REC8 have symmetrical, mutually exclusive localization on the not-yet-synapsed homologues, implying that the cohesin patterning could provide a code for homologue recognition. RAD21 transiently localizes to axial elements after the dissociation of RAD21L and REC8 in late pachytene, a period of recombination repair. Further, we show that the removal of cohesins and synaptonemal complex during late meiotic prophase is promoted by Polo-like kinase 1, which is similar to the mitotic prophase pathway.

摘要

我们鉴定了一个新的哺乳动物黏合蛋白亚基 RAD21 样蛋白(RAD21L),它与 RAD21 和 REC8 具有序列相似性。RAD21L 在早期减数分裂前期沿着轴元件定位,其时空定位方式与 REC8 或 RAD21 都不同。值得注意的是,RAD21L 和 REC8 在尚未连接的同源物上具有对称的、相互排斥的定位,这表明黏合蛋白的模式可能为同源物识别提供了一种编码。RAD21L 和 REC8 在晚期粗线期(重组修复期)解聚后,RAD21 会短暂地定位到轴元件上。此外,我们还表明,后期减数分裂前期黏合蛋白和联会复合体的去除是由 Polo 样激酶 1 促进的,这与有丝分裂前期途径相似。

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