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SUMO modifications control assembly of synaptonemal complex and polycomplex in meiosis of Saccharomyces cerevisiae

机译:SUMO修饰控制酿酒酵母减数分裂中联会复合体和多复合体的装配

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摘要

The synaptonemal complex (SC) is a proteinaceous complex that apparently mediates synapsis between homologous chromosomes during meiotic prophase. In Saccharomyces cerevisiae, the Zip1 protein is the integral component of the SC. In the absence of a DNA double-strand break or the SC initiation protein Zip3, Zip1 proteins aggregate to form a polycomplex (PC). In addition, Zip1 is also responsible for DSB-independent nonhomologous centromere coupling at early meiotic prophase. We report here that Zip3 is a SUMO (small ubiquitin-related modifier) E3 ligase and that Zip1 is a binding protein for SUMO-conjugated products. Our results also suggest that at early meiotic prophase, Zip1 interacts with Zip3-independent Smt3 conjugates (e.g., Top2) to promote nonhomologous centromere coupling. At and after mid-prophase, the Zip1 protein begins to associate with Zip3-dependent Smt3 conjugates (e.g., Red1) along meiotic chromosomes in the wild-type cell to form SCs and with Smt3 polymeric chains in the zip3 mutant to form PCs.
机译:突触复合物(SC)是一种蛋白质复合物,显然在减数分裂前期介导同源染色体之间的突触。在酿酒酵母中,Zip1蛋白是SC的组成部分。在没有DNA双链断裂或SC起始蛋白Zip3的情况下,Zip1蛋白聚集形成多复合物(PC)。此外,Zip1还负责在减数分裂前期不依赖于DSB的非同源着丝粒。我们在这里报告Zip3是SUMO(小泛素相关修饰剂)E3连接酶,而Zip1是SUMO共轭产品的结合蛋白。我们的结果还表明,在减数分裂的早期,Zip1与独立于Zip3的Smt3共轭物(例如Top2)相互作用,以促进非同源着丝粒偶联。在中期前期和之后,Zip1蛋白开始与Zip3依赖性Smt3共轭物(例如Red1)沿着野生型细胞中的减数分裂染色体形成SC,并与zip3突变体中的Smt3聚合链形成PC。

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