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减数分裂II期阻滞之后的染色体错向会导致不分离。

Chromosome malorientations after meiosis II arrest cause nondisjunction.

作者信息

Janicke Marie A, Lasko Loren, Oldenbourg Rudolf, LaFountain James R

机构信息

Department of Biological Sciences, State University of New York at Buffalo, Amherst, NY 14260, USA.

出版信息

Mol Biol Cell. 2007 May;18(5):1645-56. doi: 10.1091/mbc.e06-10-0963. Epub 2007 Feb 21.

Abstract

This study investigated the basis of meiosis II nondisjunction. Cold arrest induced a fraction of meiosis II crane fly spermatocytes to form (n + 1) and (n - 1) daughters during recovery. Live-cell liquid crystal polarized light microscope imaging showed nondisjunction was caused by chromosome malorientation. Whereas amphitely (sister kinetochore fibers to opposite poles) is normal, cold recovery induced anaphase syntely (sister fibers to the same pole) and merotely (fibers to both poles from 1 kinetochore). Maloriented chromosomes had stable metaphase positions near the equator or between the equator and a pole. Syntelics were at the spindle periphery at metaphase; their sisters disconnected at anaphase and moved all the way to a centrosome, as their strongly birefringent kinetochore fibers shortened. The kinetochore fibers of merotelics shortened little if any during anaphase, making anaphase lag common. If one fiber of a merotelic was more birefringent than the other, the less birefringent fiber lengthened with anaphase spindle elongation, often permitting inclusion of merotelics in a daughter nucleus. Meroamphitely (near amphitely but with some merotely) caused sisters to move in opposite directions. In contrast, syntely and merosyntely (near syntely but with some merotely) resulted in nondisjunction. Anaphase malorientations were more frequent after longer arrests, with particularly long arrests required to induce syntely and merosyntely.

摘要

本研究调查了减数分裂II不分离的基础。冷阻滞诱导一部分减数分裂II的大蚊精母细胞在恢复过程中形成(n + 1)和(n - 1)的子细胞。活细胞液晶偏振光显微镜成像显示,不分离是由染色体错向引起的。虽然双定向(姐妹动粒纤维连接到相反两极)是正常的,但冷恢复诱导后期出现同向(姐妹纤维连接到同一极)和单着丝粒定向(纤维从一个动粒连接到两极)。错向的染色体在赤道附近或赤道与一极之间的中期位置稳定。同向染色体在中期位于纺锤体周边;它们的姐妹染色单体在后期分离并一直移动到一个中心体,因为它们强烈双折射的动粒纤维缩短。单着丝粒定向染色体的动粒纤维在后期几乎没有缩短,导致后期滞后很常见。如果单着丝粒定向染色体的一根纤维比另一根纤维双折射更强,那么双折射较弱的纤维会随着后期纺锤体的延长而延长,这通常会使单着丝粒定向染色体包含在子核中。近双定向(接近双定向但有一些单着丝粒定向)导致姐妹染色单体向相反方向移动。相比之下,同向和近同向(接近同向但有一些单着丝粒定向)会导致不分离。较长时间的阻滞之后后期错向更频繁,诱导同向和近同向需要特别长的阻滞时间。

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