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一对假定的蛋白激酶基因(YPK1和YPK2)是酿酒酵母细胞生长所必需的。

A pair of putative protein kinase genes (YPK1 and YPK2) is required for cell growth in Saccharomyces cerevisiae.

作者信息

Chen P, Lee K S, Levin D E

机构信息

Department of Biochemistry, Johns Hopkins University, School of Public Health, Baltimore, MD 21205.

出版信息

Mol Gen Genet. 1993 Jan;236(2-3):443-7. doi: 10.1007/BF00277146.

Abstract

Probes derived from cDNAs encoding isozymes of rat protein kinase C (PKC) were used to screen the genome of the budding yeast Saccharomyces cerevisiae. We reported previously the isolation of the yeast PKC1 gene, a homolog of the alpha, beta, and gamma subspecies of mammalian PKC. Here we report the isolation and genetic characterization of a pair of previously described genes (YPK1 and YPK2) which are predicted to encode protein kinases that share 90% amino acid identity with each other and 44-46% identity with various isozymes of PKC throughout their putative catalytic domains. Deletion of YPK2 resulted in no apparent phenotypic defect, but loss of YPK1 resulted in slow growth. Cells deleted for both YPK1 and YPK2 were defective in vegetative growth, indicating that the protein kinases predicted to be encoded by these genes are functionally overlapping and play an essential role in the proliferation of yeast cells. The YPK1 gene was mapped to the left arm of chromosome XI and YPK2 was mapped to the right arm of chromosome XIII.

摘要

用源自编码大鼠蛋白激酶C(PKC)同工酶的cDNA探针筛选出芽酵母酿酒酵母的基因组。我们之前报道了酵母PKC1基因的分离,它是哺乳动物PKC的α、β和γ亚类的同源物。在此我们报道一对先前描述基因(YPK1和YPK2)的分离及遗传特征,这两个基因预计编码的蛋白激酶在其假定的催化结构域彼此具有90%的氨基酸同一性,与PKC的各种同工酶具有44 - 46%的同一性。缺失YPK2未导致明显的表型缺陷,但缺失YPK1导致生长缓慢。同时缺失YPK1和YPK2的细胞在营养生长方面存在缺陷,这表明预计由这些基因编码的蛋白激酶在功能上有重叠,并且在酵母细胞增殖中起重要作用。YPK1基因定位于染色体XI的左臂,YPK2基因定位于染色体XIII的右臂。

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