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首页> 外文期刊>Molecular biology reports >A novel Cdc20-related WD-repeat protein, Fzr1, is required for spore formation in Schizosaccharomyces pombe
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A novel Cdc20-related WD-repeat protein, Fzr1, is required for spore formation in Schizosaccharomyces pombe

机译:粟酒裂殖酵母中孢子形成需要新型与Cdc20相关的WD重复蛋白Fzr1。

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摘要

Ste9/Srw1, which shows sequence homology to Htc1 from budding yeast, is an activator of the anaphase-promoting complex (APC) in the fission yeast Schizosaccharomyces pombe. By homology search of the S. pombe genome, we identified the gene fzr1~+, which encodes the protein with the highest homology to Ste9 among five Cdc20-like proteins. Like Ste9, Fzr1 contains seven WD-repeats in its C-terminal region. In spite of this structural similarity, however, overproduction of either of these proteins cannot complement mutants lacking the other. fzr`~+ is transcribed exclusively during meiosis and sporulation, suggesting that it plays a role in these processes. In fact, the fzr1 disruptant formed aberrant asci, which contained only one or two mature spores, though meiotic nuclear divisions proceeded with kinetics similar to wild type, and meiotic segregation of chromosomes was normal, Structural alteration of spindle pole bodies, which is a prerequisite for the formation of the forespore membrane, occurred normally in fzr1△ during the second meiotic division. Localization of spore rim marker proteins fused to green fluorescent protein showed that nascent prespores were irregularly shaped, small in size and few in number in fzr1△ cells compared to wild-type cells. Furthermore, electron microscopy revealed that the outer layer of the spore walls was often missing in fzr1△ spores. These results show that Fzr1 is specifically involved in the assembly of the spore envelope and also in spore maturation. Fzr1, a structural homolog of the APC regulator, therefore plays an important role in spore morphogenesis.
机译:Ste9 / Srw1显示出与出芽酵母中Htc1的序列同源性,是裂殖酵母粟酒裂殖酵母后期促进复合物(APC)的激活剂。通过对粟酒裂殖酵母基因组的同源性搜索,我们确定了基因fzr1〜+,该基因编码与五个Cdc20样蛋白中与Ste9同源性最高的蛋白。与Ste9一样,Fzr1在其C端区域也包含七个WD重复序列。尽管有这种结构上的相似性,但是,这些蛋白质中任何一个的过量生产都不能补充缺少另一个的突变体。 fzr`〜+仅在减数分裂和孢子形成过程中转录,表明它在这些过程中起作用。实际上,尽管减数分裂核分裂以与野生型相似的动力学进行,并且减数分裂核分裂正常,染色体纺锤极体的结构改变是先决条件,但fzr1破坏物形成了异常的asci,仅包含一个或两个成熟的孢子。在第二次减数分裂分裂过程中,通常在fzr1△发生。与绿色荧光蛋白融合的孢子边缘标记蛋白的定位表明,与野生型细胞相比,fzr1△细胞中新生的孢子形状不规则,尺寸小,数量少。此外,电子显微镜检查显示,fzr1△孢子中常常缺少孢子壁的外层。这些结果表明,Fzr1特别参与孢子包膜的组装以及孢子的成熟。 Fzr1,APC调节剂的结构同源物,因此在孢子形态发生中起重要作用。

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