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DBF8, an essential gene required for efficient chromosome segregation in Saccharomyces cerevisiae.

作者信息

Houman F, Holm C

机构信息

Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.

出版信息

Mol Cell Biol. 1994 Sep;14(9):6350-60. doi: 10.1128/mcb.14.9.6350-6360.1994.

DOI:10.1128/mcb.14.9.6350-6360.1994
PMID:8065366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC359161/
Abstract

To investigate chromosome segregation in Saccharomyces cerevisiae, we examined a collection of temperature-sensitive mutants that arrest as large-budded cells at restrictive temperatures (L. H. Johnston and A. P. Thomas, Mol. Gen. Genet. 186:439-444, 1982). We characterized dbf8, a mutation that causes cells to arrest with a 2c DNA content and a short spindle. DBF8 maps to chromosome IX near the centromere, and it encodes a 36-kDa protein that is essential for viability at all temperatures. Mutational analysis reveals that three dbf8 alleles are nonsense mutations affecting the carboxy-terminal third of the encoded protein. Since all of these mutations confer temperature sensitivity, it appears that the carboxyl-terminal third of the protein is essential only at a restrictive temperature. In support of this conclusion, an insertion of URA3 at the same position also confers a temperature-sensitive phenotype. Although they show no evidence of DNA damage, dbf8 mutants exhibit increased rates of chromosome loss and nondisjunction even at a permissive temperature. Taken together, our data suggest that Dbf8p plays an essential role in chromosome segregation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5871/359161/b80b8d933fd2/molcellb00009-0753-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5871/359161/59786cc8e1c8/molcellb00009-0749-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5871/359161/b80b8d933fd2/molcellb00009-0753-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5871/359161/59786cc8e1c8/molcellb00009-0749-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5871/359161/b80b8d933fd2/molcellb00009-0753-a.jpg

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本文引用的文献

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Genetic Control of the Cell Division Cycle in Yeast: V. Genetic Analysis of cdc Mutants.酵母细胞分裂周期的遗传控制:V. cdc 突变体的遗传分析。
Genetics. 1973 Jun;74(2):267-86. doi: 10.1093/genetics/74.2.267.
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Isolation and characterization of Schizosaccharomyces pombe cutmutants that block nuclear division but not cytokinesis.裂殖酵母核分裂但不胞质分裂缺陷突变株的分离与鉴定。
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Cell cycle arrest of cdc mutants and specificity of the RAD9 checkpoint.细胞分裂周期蛋白(cdc)突变体的细胞周期停滞与RAD9检查点的特异性
酵母输入蛋白α(Srp1)在核蛋白的输入以及将蛋白酶体靶向细胞核的过程中发挥着不同的作用。
J Biol Chem. 2014 Nov 14;289(46):32339-32352. doi: 10.1074/jbc.M114.582023. Epub 2014 Oct 1.
4
Cdc48 chaperone and adaptor Ubx4 distribute the proteasome in the nucleus for anaphase proteolysis.Cdc48 伴侣蛋白和衔接蛋白 Ubx4 将蛋白酶体分配到核内进行后期蛋白酶体水解。
J Biol Chem. 2013 Dec 27;288(52):37180-91. doi: 10.1074/jbc.M113.513598. Epub 2013 Nov 13.
5
Evidence for separable functions of Srp1p, the yeast homolog of importin alpha (Karyopherin alpha): role for Srp1p and Sts1p in protein degradation.输入蛋白α(核转运蛋白α)的酵母同源物Srp1p的可分离功能的证据:Srp1p和Sts1p在蛋白质降解中的作用。
Mol Cell Biol. 2000 Aug;20(16):6062-73. doi: 10.1128/MCB.20.16.6062-6073.2000.
6
Hec1p, an evolutionarily conserved coiled-coil protein, modulates chromosome segregation through interaction with SMC proteins.Hec1p是一种进化上保守的卷曲螺旋蛋白,通过与SMC蛋白相互作用来调节染色体分离。
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9
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