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MDS1是mck1突变体的剂量抑制因子,编码糖原合酶激酶3的假定酵母同源物。

MDS1, a dosage suppressor of an mck1 mutant, encodes a putative yeast homolog of glycogen synthase kinase 3.

作者信息

Puziss J W, Hardy T A, Johnson R B, Roach P J, Hieter P

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

Mol Cell Biol. 1994 Jan;14(1):831-9. doi: 10.1128/mcb.14.1.831-839.1994.

DOI:10.1128/mcb.14.1.831-839.1994
PMID:8264650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358431/
Abstract

The yeast gene MCK1 encodes a serine/threonine protein kinase that is thought to function in regulating kinetochore activity and entry into meiosis. Disruption of MCK1 confers a cold-sensitive phenotype, a temperature-sensitive phenotype, and sensitivity to the microtubule-destabilizing drug benomyl and leads to loss of chromosomes during growth on benomyl. A dosage suppression selection was used to identify genes that, when present at high copy number, could suppress the cold-sensitive phenotype of mck1::HIS3 mutant cells. Several unique classes of clones were identified, and one of these, designated MDS1, has been characterized in some detail. Nucleotide sequence data reveal that MDS1 encodes a serine/threonine protein kinase that is highly homologous to the shaggy/zw3 kinase in Drosophila melanogaster and its functional homolog, glycogen synthase kinase 3, in rats. The presence of MDS1 in high copy number rescues both the cold-sensitive and the temperature-sensitive phenotypes, but not the benomyl-sensitive phenotype, associated with the disruption of MCK1. Analysis of strains harboring an mds1 null mutation demonstrates that MDS1 is not essential during normal vegetative growth but appears to be required for meiosis. Finally, in vitro experiments indicate that the proteins encoded by both MCK1 and MDS1 possess protein kinase activity with substrate specificity similar to that of mammalian glycogen synthase kinase 3.

摘要

酵母基因MCK1编码一种丝氨酸/苏氨酸蛋白激酶,该激酶被认为在调节动粒活性和进入减数分裂过程中发挥作用。MCK1的破坏会导致冷敏感表型、温度敏感表型以及对微管破坏药物苯菌灵敏感,并导致在苯菌灵上生长时染色体丢失。采用剂量抑制选择法来鉴定那些在高拷贝数存在时能够抑制mck1::HIS3突变细胞冷敏感表型的基因。鉴定出了几类独特的克隆,其中一个被命名为MDS1的克隆已经得到了较为详细的表征。核苷酸序列数据显示,MDS1编码一种丝氨酸/苏氨酸蛋白激酶,它与果蝇中的蓬松/zw3激酶及其在大鼠中的功能同源物糖原合酶激酶3高度同源。高拷贝数的MDS1能够挽救与MCK1破坏相关的冷敏感和温度敏感表型,但不能挽救苯菌灵敏感表型。对携带mds1无效突变的菌株进行分析表明,MDS1在正常营养生长过程中不是必需的,但在减数分裂过程中似乎是必需的。最后,体外实验表明,MCK1和MDS1编码的蛋白质都具有蛋白激酶活性,其底物特异性与哺乳动物糖原合酶激酶3相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a934/358431/8f5aa2bfdf70/molcellb00001-0862-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a934/358431/8f5aa2bfdf70/molcellb00001-0862-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a934/358431/8f5aa2bfdf70/molcellb00001-0862-a.jpg

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