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本文引用的文献

1
Physical maps of the six smallest chromosomes of Saccharomyces cerevisiae at a resolution of 2.6 kilobase pairs.酿酒酵母六条最小染色体的物理图谱,分辨率为2.6千碱基对。
Genetics. 1993 May;134(1):81-150. doi: 10.1093/genetics/134.1.81.
2
Coupling of cell identity to signal response in yeast: interaction between the alpha 1 and STE12 proteins.酵母中细胞身份与信号反应的偶联:α1蛋白与STE12蛋白之间的相互作用
Genes Dev. 1993 Aug;7(8):1584-97. doi: 10.1101/gad.7.8.1584.
3
Genetic interactions between KAR2 and SEC63, encoding eukaryotic homologues of DnaK and DnaJ in the endoplasmic reticulum.KAR2与SEC63之间的遗传相互作用,它们在内质网中编码DnaK和DnaJ的真核同源物。
Mol Biol Cell. 1993 Nov;4(11):1145-59. doi: 10.1091/mbc.4.11.1145.
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Elements of the yeast pheromone response pathway required for filamentous growth of diploids.二倍体丝状生长所需的酵母信息素反应途径的元件。
Science. 1993 Dec 10;262(5140):1741-4. doi: 10.1126/science.8259520.
5
Localization of the Kar3 kinesin heavy chain-related protein requires the Cik1 interacting protein.Kar3驱动蛋白重链相关蛋白的定位需要Cik1相互作用蛋白。
J Cell Biol. 1994 Feb;124(4):507-19. doi: 10.1083/jcb.124.4.507.
6
Nuclear congression and membrane fusion: two distinct events in the yeast karyogamy pathway.细胞核汇聚与膜融合:酵母核配途径中的两个不同事件。
J Cell Biol. 1994 Aug;126(4):911-23. doi: 10.1083/jcb.126.4.911.
7
KAR3-encoded kinesin is a minus-end-directed motor that functions with centromere binding proteins (CBF3) on an in vitro yeast kinetochore.由KAR3编码的驱动蛋白是一种向负端移动的分子马达,它与体外酵母动粒上的着丝粒结合蛋白(CBF3)共同发挥作用。
Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7212-6. doi: 10.1073/pnas.91.15.7212.
8
The karyogamy gene KAR2 and novel proteins are required for ER-membrane fusion.核融合基因KAR2和新型蛋白质是内质网膜融合所必需的。
Cell. 1994 Jul 15;78(1):87-98. doi: 10.1016/0092-8674(94)90575-4.
9
Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae.酿酒酵母中基因表达、蛋白质定位及基因敲除的大规模分析。
Genes Dev. 1994 May 1;8(9):1087-105. doi: 10.1101/gad.8.9.1087.
10
G1 cyclins CLN1 and CLN2 repress the mating factor response pathway at Start in the yeast cell cycle.G1 细胞周期蛋白CLN1和CLN2在酵母细胞周期的起始点抑制交配因子反应途径。
Genes Dev. 1994 May 1;8(9):1058-70. doi: 10.1101/gad.8.9.1058.

Kar4p,酵母信息素反应途径中一种特定于核融合的组分。

Kar4p, a karyogamy-specific component of the yeast pheromone response pathway.

作者信息

Kurihara L J, Stewart B G, Gammie A E, Rose M D

机构信息

Department of Molecular Biology, Princeton University, New Jersey 08544, USA.

出版信息

Mol Cell Biol. 1996 Aug;16(8):3990-4002. doi: 10.1128/MCB.16.8.3990.

DOI:10.1128/MCB.16.8.3990
PMID:8754797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC231395/
Abstract

Karyogamy is the process whereby two haploid nuclei fuse to form a diploid nucleus during mating in Saccharomyces cerevisiae. Here, we describe the characterization of the KAR4 gene, previously identified in a screen for new nuclear fusion-defective mutants. During mating, kar4 mutants were defective for the microtubule-dependent movement of nuclei, a phenotype identical to that of mutations in KAR3 and CIK1. Consistent with its mutant phenotype, we found that the kar4 mutation resulted in failure to induce KAR3 and CIK1 mRNA during mating. Expression of KAR3 and CIK1 under independent regulatory control suppressed the kar4 defect, indicating that KAR4 is required primarily for the induction of KAR3 and CIK1. KAR4 was also required for meiosis, during which it may regulate KAR3; however, mitotic expression of KAR3 and CIK1 during S/G2 phase was independent of KAR4. A 30-bp region upstream of KAR3 conferred both KAR4- and STE12-dependent induction by mating pheromone. This region contained one moderate and two weak matches to the consensus pheromone response element to which the Ste12p transcriptional activator binds and five repeats of the sequence CAAA(A). Overproduction of Ste12p suppressed the kar4 defect in KAR3 induction and nuclear fusion. In contrast, Ste12p-independent expression of Kar4p did not alleviate the requirement for Ste12p during KAR3 induction. We propose that Kar4p assists Ste12p in the pheromone-dependent expression of KAR3 and CIK1. KAR4 defines a novel level of regulation for the pheromone response pathway, acting at a subset of Stel2p-inducible genes required for karyogamy.

摘要

核融合是酿酒酵母在交配过程中两个单倍体细胞核融合形成二倍体细胞核的过程。在此,我们描述了KAR4基因的特征,该基因先前在筛选新的核融合缺陷突变体时被鉴定出来。在交配过程中,kar4突变体在细胞核的微管依赖性运动方面存在缺陷,这一表型与KAR3和CIK1基因突变的表型相同。与其突变表型一致,我们发现kar4突变导致在交配过程中无法诱导KAR3和CIK1 mRNA的表达。在独立调控下表达KAR3和CIK1可抑制kar4缺陷,表明KAR4主要是诱导KAR3和CIK1所必需的。减数分裂也需要KAR4,在此过程中它可能调控KAR3;然而,在S/G2期KAR3和CIK1的有丝分裂表达不依赖于KAR4。KAR3上游30 bp的区域赋予了交配信息素诱导的KAR4依赖性和STE12依赖性。该区域包含一个与Ste12p转录激活因子结合的共有信息素反应元件的中度匹配和两个弱匹配,以及序列CAAA(A)的五个重复。Ste12p的过量表达抑制了kar4在KAR3诱导和核融合方面的缺陷。相反,Kar4p的不依赖于Ste12p的表达并不能减轻KAR3诱导过程中对Ste12p的需求。我们提出Kar4p在信息素依赖性的KAR3和CIK1表达中协助Ste12p。KAR4定义了信息素反应途径的一种新的调控水平,作用于核融合所需的一部分Ste12p诱导基因。