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姐妹染色单体黏连性和结构在减数分裂行为中的作用。

The role of sister chromatid cohesiveness and structure in meiotic behaviour.

作者信息

Giménez-Abián J F, Clarke D J, García de la Vega C, Giménez-Martín G

机构信息

Centro de Investigaciones Biológicas, CSIC, Velázquez 144, E-28006, Madrid, Spain.

出版信息

Chromosoma. 1997 Dec;106(7):422-34. doi: 10.1007/s004120050264.

Abstract

Sister chromatid cores, kinetochores and the connecting strand between sister kinetochores were differentially silver stained to analyse the behaviour of these structures during meiosis in normal and two spontaneous desynaptic individuals of Chorthippus jucundus (Orthoptera). In these desynaptic individuals most of the chromosomes appear as univalents and orient equationally in the first meiotic division. Despite this abnormal segregation pattern, the changes in chromosome structure follow the same timing as in normal individuals and seem to be strictly phase dependent. Chromosomes in the first prometaphase have associated sister kinetochores and sister chromatid cores that lie in the chromosome midline; we propose that this promotes the initial monopolar orientation of chromosomes. However, the requirements of tension for stable attachment to the spindle force the autosomal univalents to acquire amphitelic orientation. Sister kinetochores behave in a chromosome orientation-dependent manner and, in the first metaphase, they appear to be interconnected by a strand that can be detected by silver impregnation, as seen in the second metaphase of wild-type individuals. The disappearance of the sister kinetochore-connecting strand, needed for equational chromatid segregation, however, can only take place in the second meiotic division. This connecting strand is ultimately responsible for the inability of chromosomes to segregate sister chromatids in the first anaphase.

摘要

对姐妹染色单体核心、着丝粒以及姐妹着丝粒之间的连接链进行差异银染,以分析这些结构在正常和两种自发去联会的短翅草螽(直翅目)减数分裂过程中的行为。在这些去联会个体中,大多数染色体呈现单价体状态,并在第一次减数分裂中进行均等定向。尽管存在这种异常的分离模式,但染色体结构的变化与正常个体遵循相同的时间进程,且似乎严格依赖于阶段。第一次前中期的染色体具有相连的姐妹着丝粒和位于染色体中线的姐妹染色单体核心;我们认为这促进了染色体最初的单极定向。然而,为稳定附着于纺锤体而对张力的需求迫使常染色体单价体获得双着丝粒定向。姐妹着丝粒的行为依赖于染色体的定向方式,并且在第一次中期,它们似乎通过一条可通过银染检测到的链相互连接,就像在野生型个体的第二次中期所观察到的那样。然而,姐妹着丝粒连接链的消失,这是姐妹染色单体均等分离所必需的,只能在第二次减数分裂中发生。这条连接链最终导致染色体在第一次后期无法分离姐妹染色单体。

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