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A chromosomal gene required for killer plasmid expression, mating, and spore maturation in Saccharomyces cerevisiae.酿酒酵母中杀伤质粒表达、交配和孢子成熟所需的一种染色体基因。
Proc Natl Acad Sci U S A. 1976 Jun;73(6):2061-5. doi: 10.1073/pnas.73.6.2061.
2
Two chromosomal genes required for killing expression in killer strains of Saccharomyces cerevisiae.酿酒酵母杀伤菌株中杀伤表达所需的两个染色体基因。
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Twenty-six chromosomal genes needed to maintain the killer double-stranded RNA plasmid of Saccharomyces cerevisiae.维持酿酒酵母杀伤性双链RNA质粒需要26个染色体基因。
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An α-mating-type-specific mutation causing specific defect in sexual agglutinability in the yeast Saccharomyces cerevisiae.一个α-交配型特异性突变导致酵母酿酒酵母中性凝集能力的特定缺陷。
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Viruses and prions of Saccharomyces cerevisiae.酿酒酵母的病毒和朊病毒。
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The requirement for the highly conserved G-1 residue of Saccharomyces cerevisiae tRNAHis can be circumvented by overexpression of tRNAHis and its synthetase.高度保守的酿酒酵母 tRNAHis 的 G-1 残基要求可以通过过量表达 tRNAHis 和其合成酶来规避。
RNA. 2010 May;16(5):1068-77. doi: 10.1261/rna.2087510. Epub 2010 Apr 1.
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Structural basis for the kexin-like serine protease from Aeromonas sobria as sepsis-causing factor.嗜水气单胞菌中类克新丝氨酸蛋白酶作为败血症致病因素的结构基础。
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本文引用的文献

1
Genetic Mapping in Saccharomyces IV. Mapping of Temperature-Sensitive Genes and Use of Disomic Strains in Localizing Genes.酵母的遗传图谱 IV. 温度敏感基因的图谱绘制以及在定位基因中的二倍体菌株的使用。
Genetics. 1973 May;74(1):33-54. doi: 10.1093/genetics/74.1.33.
2
Periodic density fluctuation during the yeast cell cycle and the selection of synchronous cultures.酵母细胞周期中的周期性密度波动与同步培养物的选择。
J Bacteriol. 1970 Dec;104(3):1280-5. doi: 10.1128/jb.104.3.1280-1285.1970.
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Mitosis in the yeast Lipomyces lipofer.产脂油脂酵母中的有丝分裂。
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4
Isolation of beta-dihydroequilin and alpha-dihydroequilenin from the urine of pregnant mares.从怀孕母马尿液中分离出β-二氢马萘雌酮和α-二氢马萘雌烯酮。
Nature. 1956 Apr 21;177(4512):753. doi: 10.1038/177753a0.
5
Sporulation of yeast harvested during logarithmic growth.对数生长期收获的酵母的孢子形成。
J Bacteriol. 1969 May;98(2):831-2. doi: 10.1128/jb.98.2.831-832.1969.
6
The inheritance of the killer character in yeast.酵母中杀伤特性的遗传
Genet Res. 1969 Feb;13(1):71-83. doi: 10.1017/s0016672300002743.
7
Studies on the nature of the killer factor produced by Saccharomyces cerevisiae.酿酒酵母产生的杀伤因子的性质研究。
J Gen Microbiol. 1968 Apr;51(1):115-26. doi: 10.1099/00221287-51-1-115.
8
DNA synthesis during yeast sporulation: genetic control of an early developmental event.酵母孢子形成过程中的DNA合成:早期发育事件的遗传控制
Science. 1970 Apr 24;168(3930):493-4. doi: 10.1126/science.168.3930.493.
9
Genetic control of the cell division cycle in yeast. IV. Genes controlling bud emergence and cytokinesis.酵母细胞分裂周期的遗传控制。IV. 控制芽出现和胞质分裂的基因。
Exp Cell Res. 1971 Dec;69(2):265-76. doi: 10.1016/0014-4827(71)90223-0.
10
Genes controlling meiosis and spore formation in yeast.控制酵母减数分裂和孢子形成的基因。
Genetics. 1974 Sep;78(1):215-25. doi: 10.1093/genetics/78.1.215.

酿酒酵母中杀伤质粒表达、交配和孢子成熟所需的一种染色体基因。

A chromosomal gene required for killer plasmid expression, mating, and spore maturation in Saccharomyces cerevisiae.

作者信息

Leibowitz M J, Wickner R B

出版信息

Proc Natl Acad Sci U S A. 1976 Jun;73(6):2061-5. doi: 10.1073/pnas.73.6.2061.

DOI:10.1073/pnas.73.6.2061
PMID:778853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC430448/
Abstract

"Killer" strains of Saccharomyces cerevisiae are those that harbor a double-stranded RNA plasmid and secrete a toxin that kills only strains not carrying this plasmid (sensitives). Two chromosomal genes (kex1 and kex2) are required for the secretion of toxin by plasmid-carrying strains. The kex2 gene, which maps at a site distinct from the mating-type locus, is also required for normal mating by alpha strains and meiotic sporulation in all strains. Strains that are alpha mating-type and kex2 fail to secrete the pheromone alpha-factor or to respond to the alpha-factor II pheromone which causes a morphological change, but they do respond to alpha-factor I which causes G1 arrest in alpha cells. Strains that are alpha mating-type and kex2 show no defect in mating; pheromone secretion, or response to alpha-factor. Diploids that are homozygous for the kex2 mutation, unlike wildtype or heterozygous diploids, fail to undergo sporulation, with the defect occurring in the final spore maturation stage. These same defects in the sexual cycle are present in all kex2 mutants independent of the presence of the "killer" plasmid.

摘要

酿酒酵母的“杀手”菌株是那些携带双链RNA质粒并分泌一种毒素的菌株,这种毒素只会杀死不携带该质粒的菌株(敏感菌株)。携带质粒的菌株分泌毒素需要两个染色体基因(kex1和kex2)。kex2基因定位于与交配型位点不同的位置,α菌株正常交配以及所有菌株减数分裂产孢也需要该基因。α交配型且kex2缺陷的菌株无法分泌信息素α因子,也无法对引起形态变化的α因子II信息素作出反应,但它们对引起α细胞G1期停滞的α因子I有反应。α交配型且kex2缺陷的菌株在交配、信息素分泌或对α因子的反应方面没有缺陷。与野生型或杂合二倍体不同,kex2突变纯合的二倍体无法进行孢子形成,缺陷发生在最终的孢子成熟阶段。所有kex2突变体在有性生殖周期中都存在这些相同的缺陷,与“杀手”质粒的存在无关。