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NDC1:酵母纺锤体极体复制所需的核周组分。

NDC1: a nuclear periphery component required for yeast spindle pole body duplication.

作者信息

Winey M, Hoyt M A, Chan C, Goetsch L, Botstein D, Byers B

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Colorado-Boulder 80309-0347.

出版信息

J Cell Biol. 1993 Aug;122(4):743-51. doi: 10.1083/jcb.122.4.743.

Abstract

The spindle pole body (SPB) of Saccharomyces cerevisiae serves as the centrosome in this organism, undergoing duplication early in the cell cycle to generate the two poles of the mitotic spindle. The conditional lethal mutation ndc1-1 has previously been shown to cause asymmetric segregation, wherein all the chromosomes go to one pole of the mitotic spindle (Thomas, J. H., and D. Botstein. 1986. Cell. 44:65-76). Examination by electron microscopy of mutant cells subjected to the nonpermissive temperature reveals a defect in SPB duplication. Although duplication is seen to occur, the nascent SPB fails to undergo insertion into the nuclear envelope. The parental SPB remains functional, organizing a monopolar spindle to which all the chromosomes are presumably attached. Order-of-function experiments reveal that the NDC1 function is required in G1 after alpha-factor arrest but before the arrest caused by cdc34. Molecular analysis shows that the NDC1 gene is essential and that it encodes a 656 amino acid protein (74 kD) with six or seven putative transmembrane domains. This evidence for membrane association is further supported by immunofluorescent localization of the NDC1 product to the vicinity of the nuclear envelope. These findings suggest that the NDC1 protein acts within the nuclear envelope to mediate insertion of the nascent SPB.

摘要

酿酒酵母的纺锤体极体(SPB)在该生物体中充当中心体,在细胞周期早期进行复制以产生有丝分裂纺锤体的两极。条件致死突变体ndc1-1先前已被证明会导致不对称分离,即所有染色体都移向有丝分裂纺锤体的一极(Thomas, J. H., and D. Botstein. 1986. Cell. 44:65 - 76)。对处于非允许温度的突变细胞进行电子显微镜检查发现SPB复制存在缺陷。尽管可以看到复制发生,但新生的SPB未能插入核膜。亲代SPB仍保持功能,组织形成一个单极纺锤体,所有染色体可能都附着在该纺锤体上。功能顺序实验表明,NDC1功能在α因子阻断后的G1期、但在cdc34引起的阻断之前是必需的。分子分析表明,NDC1基因是必需的,它编码一种含有六个或七个推定跨膜结构域的656个氨基酸的蛋白质(74 kD)。NDC1产物在核膜附近的免疫荧光定位进一步支持了这种与膜相关的证据。这些发现表明,NDC1蛋白在核膜内起作用,介导新生SPB的插入。

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