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减数分裂黏连蛋白在裂殖酵母减数分裂前期调节染色体压缩。

Meiotic cohesins modulate chromosome compaction during meiotic prophase in fission yeast.

作者信息

Ding Da-Qiao, Sakurai Nobuko, Katou Yuki, Itoh Takehiko, Shirahige Katsuhiko, Haraguchi Tokuko, Hiraoka Yasushi

机构信息

Cell Biology Group, Kansai Advanced Research Center, National Institute of Information and Communications Technology, Kobe 651-2492, Japan.

出版信息

J Cell Biol. 2006 Aug 14;174(4):499-508. doi: 10.1083/jcb.200605074. Epub 2006 Aug 7.

Abstract

The meiotic cohesin Rec8 is required for the stepwise segregation of chromosomes during the two rounds of meiotic division. By directly measuring chromosome compaction in living cells of the fission yeast Schizosaccharomyces pombe, we found an additional role for the meiotic cohesin in the compaction of chromosomes during meiotic prophase. In the absence of Rec8, chromosomes were decompacted relative to those of wild-type cells. Conversely, loss of the cohesin-associated protein Pds5 resulted in hypercompaction. Although this hypercompaction requires Rec8, binding of Rec8 to chromatin was reduced in the absence of Pds5, indicating that Pds5 promotes chromosome association of Rec8. To explain these observations, we propose that meiotic prophase chromosomes are organized as chromatin loops emanating from a Rec8-containing axis: the absence of Rec8 disrupts the axis, resulting in disorganized chromosomes, whereas reduced Rec8 loading results in a longitudinally compacted axis with fewer attachment points and longer chromatin loops.

摘要

减数分裂黏连蛋白Rec8是两轮减数分裂过程中染色体逐步分离所必需的。通过直接测量裂殖酵母粟酒裂殖酵母活细胞中的染色体压缩情况,我们发现减数分裂黏连蛋白在减数分裂前期染色体压缩中还有额外作用。在缺乏Rec8的情况下,染色体相对于野生型细胞的染色体解压缩。相反,黏连蛋白相关蛋白Pds5的缺失导致超压缩。尽管这种超压缩需要Rec8,但在缺乏Pds5的情况下,Rec8与染色质的结合减少,表明Pds5促进Rec8与染色体的结合。为了解释这些观察结果,我们提出减数分裂前期染色体被组织成从含Rec8的轴发出的染色质环:Rec8的缺失破坏了轴,导致染色体无序,而Rec8负载减少导致纵向压缩的轴,附着点减少且染色质环更长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fc6/2064256/1c8665df7660/jcb1740499f01.jpg

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