Rec8凝聚素复合物的乙酰化调节减数分裂过程中的还原染色体分离。

IF 3.3 2区 生物学 Q1 BIOLOGY Life Science Alliance Pub Date : 2024-04-04 DOI:10.26508/lsa.202402606
Ziqiang Li, Yu Liu, Andrew W Jones, Yoshinori Watanabe
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引用次数: 0

摘要

在裂殖酵母有丝分裂过程中,乙酰转移酶 Eso1 在建立姐妹染色单体内聚力和正确的染色体分离方面发挥着关键作用。Eso1 在凝聚素亚基 Psm3 的两个保守赖氨酸残基 K105 和 K106 上对凝聚素复合物进行乙酰化。虽然 Eso1 也有助于减数分裂过程中的还原染色体分离,但其潜在的分子机制仍然难以捉摸。在这里,我们纯化了定位于中心粒的减数分裂特异性 Rec8 凝聚素复合物,并在 Psm3-K1013 处发现了一种新的乙酰化,这种乙酰化主要依赖于减数分裂动核因子 meikin(Moa1)。我们的分子遗传学分析表明,Psm3-K1013乙酰化与Psm3-K105和K106的典型乙酰化相互配合,在减数分裂过程中建立还原染色体分离中起着至关重要的作用。
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Acetylation of Rec8 cohesin complexes regulates reductional chromosome segregation in meiosis.
For establishing sister chromatid cohesion and proper chromosome segregation in mitosis in fission yeast, the acetyltransferase Eso1 plays a key role. Eso1 acetylates cohesin complexes, at two conserved lysine residues K105 and K106 of the cohesin subunit Psm3. Although Eso1 also contributes to reductional chromosome segregation in meiosis, the underlying molecular mechanisms have remained elusive. Here, we purified meiosis-specific Rec8 cohesin complexes localized at centromeres and identified a new acetylation at Psm3-K1013, which largely depends on the meiotic kinetochore factor meikin (Moa1). Our molecular genetic analyses indicate that Psm3-K1013 acetylation cooperates with canonical acetylation at Psm3-K105 and K106, and plays a crucial role in establishing reductional chromosome segregation in meiosis.
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来源期刊
Life Science Alliance
Life Science Alliance Agricultural and Biological Sciences-Plant Science
CiteScore
5.80
自引率
2.30%
发文量
241
审稿时长
10 weeks
期刊介绍: Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.
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