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在裂殖酵母粟酒裂殖酵母中鉴定一种新型酪蛋白激酶-1同源物。

Identification of a novel casein kinase-1 homolog in fission yeast Schizosaccharomyces pombe.

作者信息

Kitamura K, Yamashita I

机构信息

Center for Gene Science, Hiroshima University, Kagamiyama 1-4-2, Higashi-Hiroshima 739-8527, Japan.

出版信息

Gene. 1998 Jul 3;214(1-2):131-7. doi: 10.1016/s0378-1119(98)00203-0.

Abstract

Fission yeast cells lacking either the ste9+- or rum1+ function cannot enter the cell differentiation pathway upon nutritional starvation. Sterility in both mutants is suppressed by the srs1-S41 mutation. A gene encoding a novel casein kinase-1 (CK1) isoform, cki3+, was isolated as a high-copy-number suppressor gene of the srs1 mutation. Cki3 protein is structurally more related to the Cki/Yck subfamily proteins than those of the Hhp/Hrr25 subfamily. A mutant cki3 gene in which a highly conserved lysine residue in the kinase subdomain II was substituted to arginine lost the ability to recover the growth defect in the srs1 mutant, indicating that catalytic activity was necessary for suppression. Gene disruption revealed that cki3+ was dispensable for cell viability, and cells lacking functional cki3+ exhibited no characteristic phenotype. Thus, S. pombe has three highly related CK1 isoforms (Cki1, Cki2 and Cki3), but none of them has an essential function.

摘要

缺乏ste9⁺或rum1⁺功能的裂殖酵母细胞在营养饥饿时无法进入细胞分化途径。两种突变体的不育性都被srs1 - S41突变所抑制。一个编码新型酪蛋白激酶-1(CK1)同工型cki3⁺的基因被分离出来,作为srs1突变的高拷贝数抑制基因。与Hhp/Hrr25亚家族的蛋白相比,Cki3蛋白在结构上与Cki/Yck亚家族蛋白的关系更为密切。激酶亚结构域II中一个高度保守的赖氨酸残基被精氨酸取代的cki3突变基因失去了恢复srs1突变体生长缺陷的能力,这表明催化活性对于抑制是必需的。基因敲除显示cki3⁺对细胞活力并非必需,缺乏功能性cki3⁺的细胞没有表现出特征性表型。因此,粟酒裂殖酵母有三种高度相关的CK1同工型(Cki1、Cki2和Cki3),但它们都没有必需功能。

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