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驱动蛋白-14对嗜热四膜虫有丝分裂和减数分裂过程中的染色体分离很重要。

Kinesin-14 is Important for Chromosome Segregation During Mitosis and Meiosis in the Ciliate Tetrahymena thermophila.

作者信息

Kushida Yasuharu, Takaine Masak, Nakano Kentaro, Sugai Toshiro, Vasudevan Krishna Kumar, Guha Mayukh, Jiang Yu-Yang, Gaertig Jacek, Numata Osamu

机构信息

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8572, Japan.

Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, 371-8512, Japan.

出版信息

J Eukaryot Microbiol. 2017 May;64(3):293-307. doi: 10.1111/jeu.12366. Epub 2016 Sep 23.

Abstract

Ciliates such as Tetrahymena thermophila have two distinct nuclei within one cell: the micronucleus that undergoes mitosis and meiosis and the macronucleus that undergoes amitosis, a type of nuclear division that does not involve a bipolar spindle, but still relies on intranuclear microtubules. Ciliates provide an opportunity for the discovery of factors that specifically contribute to chromosome segregation based on a bipolar spindle, by identification of factors that affect the micronuclear but not the macronuclear division. Kinesin-14 is a conserved minus-end directed microtubule motor that cross-links microtubules and contributes to the bipolar spindle sizing and organization. Here, we use homologous DNA recombination to knock out genes that encode kinesin-14 orthologues (KIN141, KIN142) in Tetrahymena. A loss of KIN141 led to severe defects in the chromosome segregation during both mitosis and meiosis but did not affect amitosis. A loss of KIN141 altered the shape of the meiotic spindle in a way consistent with the KIN141's contribution to the organization of the spindle poles. EGFP-tagged KIN141 preferentially accumulated at the spindle poles during the meiotic prophase and metaphase I. Thus, in ciliates, kinesin-14 is important for nuclear divisions that involve a bipolar spindle.

摘要

诸如嗜热四膜虫这样的纤毛虫在一个细胞内有两个不同的细胞核

进行有丝分裂和减数分裂的微核,以及进行无丝分裂的大核,无丝分裂是一种核分裂类型,不涉及双极纺锤体,但仍依赖于核内微管。通过鉴定影响微核分裂而不影响大核分裂的因子,纤毛虫为发现特别有助于基于双极纺锤体的染色体分离的因子提供了机会。驱动蛋白-14是一种保守的指向微管负端的微管马达,它使微管交联并有助于双极纺锤体的大小确定和组织。在这里,我们使用同源DNA重组来敲除嗜热四膜虫中编码驱动蛋白-14直向同源物(KIN141、KIN142)的基因。KIN141的缺失导致有丝分裂和减数分裂期间染色体分离出现严重缺陷,但不影响无丝分裂。KIN141的缺失以一种与KIN141对纺锤体极组织的贡献一致的方式改变了减数分裂纺锤体的形状。在减数分裂前期和中期I,带有增强绿色荧光蛋白(EGFP)标签的KIN141优先聚集在纺锤体极。因此,在纤毛虫中,驱动蛋白-14对于涉及双极纺锤体的核分裂很重要。

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