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鉴定cut8+和cek1+,一个新型蛋白激酶基因,其可弥补阻止后期的裂殖酵母突变。

Identification of cut8+ and cek1+, a novel protein kinase gene, which complement a fission yeast mutation that blocks anaphase.

作者信息

Samejima I, Yanagida M

机构信息

Department of Biophysics, Faculty of Science, Kyoto University, Japan.

出版信息

Mol Cell Biol. 1994 Sep;14(9):6361-71. doi: 10.1128/mcb.14.9.6361-6371.1994.

Abstract

The fission yeast Schizosaccharomyces pombe [corrected] temperature sensitivity cut8-563 mutation causes chromosome overcondensation and short spindle formation in the absence of sister chromatid separation. The cut8-563 mutation allows cytokinesis before the completion of anaphase, thus producing cells with a cut phenotype. The cut8+ gene product may be required for normal progression of anaphase. Diploidization occurs at the restrictive temperature, and 60 to 70% of the cells surviving after two generations are diploid. These phenotypes are reminiscent of those of budding yeast (Saccharomyces cerevisiae) ctf13 and ctf14 (ndc10) mutations. The cut8+ gene, isolated by complementation of the mutant, predicts a 262-amino-acid protein; the amino and carboxy domains are hydrophilic, while the central domain contains several hydrophobic stretches. It has a weak overall similarity to the budding yeast DBF8 gene product. DBF8 is an essential gene whose mutations result in delay in mitotic progression and chromosome instability. Anti-cut8 antibodies detect a 33-kDa polypeptide. Two multicopy suppressor genes for cut8-563 are identified. They are the cut1+ gene essential for nuclear division, and a new gene (designated cek1+) which encodes a novel protein kinase. The cek1+ gene product is unusually large (1,309 amino acids) and has a 112-amino-acid additional sequence in the kinase domain. The cek1+ gene is not an essential gene. Protein phosphorylation by cek1 may facilitate the progression of anaphase through direct or indirect interaction with the cut8 protein.

摘要

粟酒裂殖酵母(Schizosaccharomyces pombe)[已修正]的温度敏感性cut8 - 563突变在没有姐妹染色单体分离的情况下会导致染色体过度浓缩和短纺锤体形成。cut8 - 563突变允许在后期完成之前进行胞质分裂,从而产生具有cut表型的细胞。正常后期进程可能需要cut8 +基因产物。在限制温度下会发生二倍体化,两代后存活的细胞中有60%至70%是二倍体。这些表型让人联想到芽殖酵母(Saccharomyces cerevisiae)的ctf13和ctf14(ndc10)突变。通过对突变体进行互补分离得到的cut8 +基因预测有一个262个氨基酸的蛋白质;氨基和羧基结构域是亲水的,而中央结构域包含几个疏水片段。它与芽殖酵母DBF8基因产物有较弱的整体相似性。DBF8是一个必需基因,其突变会导致有丝分裂进程延迟和染色体不稳定。抗cut8抗体可检测到一种33 kDa的多肽。鉴定出了cut8 - 563的两个多拷贝抑制基因。它们是核分裂所必需的cut1 +基因,以及一个编码新型蛋白激酶的新基因(命名为cek1 +)。cek1 +基因产物异常大(1309个氨基酸),并且在激酶结构域中有一个112个氨基酸的附加序列。cek1 +基因不是必需基因。cek1介导的蛋白质磷酸化可能通过与cut8蛋白直接或间接相互作用促进后期进程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01ba/359162/72c2acac3d18/molcellb00009-0759-a.jpg

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