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本文引用的文献

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NDT80 and the meiotic recombination checkpoint regulate expression of middle sporulation-specific genes in Saccharomyces cerevisiae.NDT80和减数分裂重组检查点调节酿酒酵母中孢子形成中期特异性基因的表达。
Mol Cell Biol. 1998 Oct;18(10):5750-61. doi: 10.1128/MCB.18.10.5750.
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Gametogenesis in yeast is regulated by a transcriptional cascade dependent on Ndt80.酵母中的配子发生受依赖于Ndt80的转录级联调控。
Mol Cell. 1998 Apr;1(5):685-96. doi: 10.1016/s1097-2765(00)80068-4.
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Analysis of a meiosis-specific URS1 site: sequence requirements and involvement of replication protein A.减数分裂特异性URS1位点的分析:序列要求及复制蛋白A的作用
Mol Cell Biol. 1997 Jul;17(7):3536-46. doi: 10.1128/MCB.17.7.3536.
4
Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters.Ume6介导的基因沉默作用涉及到一个包含Sin3共抑制因子和Rpd3组蛋白去乙酰化酶的复合物被招募到目标启动子上。
Cell. 1997 May 2;89(3):365-71. doi: 10.1016/s0092-8674(00)80217-2.
5
The CDK-activating kinase CAK1 can dosage suppress sporulation defects of smk1 MAP kinase mutants and is required for spore wall morphogenesis in Saccharomyces cerevisiae.细胞周期蛋白依赖性激酶激活激酶CAK1可以在剂量上抑制smk1丝裂原活化蛋白激酶突变体的孢子形成缺陷,并且是酿酒酵母孢子壁形态发生所必需的。
EMBO J. 1997 Mar 17;16(6):1305-17. doi: 10.1093/emboj/16.6.1305.
6
Regulation of gene expression during meiosis in Saccharomyces cerevisiae: SPR3 is controlled by both ABFI and a new sporulation control element.酿酒酵母减数分裂过程中的基因表达调控:SPR3受ABFI和一个新的孢子形成控制元件共同调控。
Mol Cell Biol. 1997 Mar;17(3):1152-9. doi: 10.1128/MCB.17.3.1152.
7
An Ssn6-Tup1-dependent negative regulatory element controls sporulation-specific expression of DIT1 and DIT2 in Saccharomyces cerevisiae.一个依赖Ssn6-Tup1的负调控元件控制酿酒酵母中DIT1和DIT2的孢子形成特异性表达。
Mol Cell Biol. 1997 Jan;17(1):123-34. doi: 10.1128/MCB.17.1.123.
8
A quantitative model for the cdc2 control of S phase and mitosis in fission yeast.裂殖酵母中 cdc2 对 S 期和有丝分裂控制的定量模型。
Trends Genet. 1996 Sep;12(9):345-50.
9
Participation of the yeast activator Abf1 in meiosis-specific expression of the HOP1 gene.酵母激活因子Abf1参与HOP1基因的减数分裂特异性表达。
Mol Cell Biol. 1996 Jun;16(6):2777-86. doi: 10.1128/MCB.16.6.2777.
10
Induction of meiosis in Saccharomyces cerevisiae depends on conversion of the transcriptional represssor Ume6 to a positive regulator by its regulated association with the transcriptional activator Ime1.酿酒酵母减数分裂的诱导取决于转录抑制因子Ume6通过与转录激活因子Ime1的调控结合而转变为正调控因子。
Mol Cell Biol. 1996 May;16(5):2518-26. doi: 10.1128/MCB.16.5.2518.

酿酒酵母减数分裂发育过程中SMK1丝裂原活化蛋白激酶基因的转录调控。

Transcriptional regulation of the SMK1 mitogen-activated protein kinase gene during meiotic development in Saccharomyces cerevisiae.

作者信息

Pierce M, Wagner M, Xie J, Gailus-Durner V, Six J, Vershon A K, Winter E

机构信息

Department of Biochemistry and Molecular Pharmacology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Mol Cell Biol. 1998 Oct;18(10):5970-80. doi: 10.1128/MCB.18.10.5970.

DOI:10.1128/MCB.18.10.5970
PMID:9742114
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC109183/
Abstract

Meiotic development (sporulation) in Saccharomyces cerevisiae is characterized by an ordered pattern of gene expression, with sporulation-specific genes classified as early, middle, mid-late, or late depending on when they are expressed. SMK1 encodes a mitogen-activated protein kinase required for spore morphogenesis that is expressed as a middle sporulation-specific gene. Here, we identify the cis-acting DNA elements that regulate SMK1 transcription and characterize the phenotypes of mutants with altered expression patterns. The SMK1 promoter contains an upstream activating sequence (UASS) that specifically interacts with the transcriptional activator Abf1p. The Abf1p-binding sites from the early HOP1 and the middle SMK1 promoters are functionally interchangeable, demonstrating that these elements do not play a direct role in their differential transcriptional timing. Timing of SMK1 expression is determined by another cis-acting DNA sequence termed MSE (for middle sporulation element). The MSE is required not only for activation of SMK1 transcription during middle sporulation but also for its repression during vegetative growth and early meiosis. In addition, the SMK1 MSE can repress vegetative expression in the context of the HOP1 promoter and convert HOP1 from an early to a middle gene. SMK1 function is not contingent on its tight transcriptional regulation as a middle sporulation-specific gene. However, promoter mutants with different quantitative defects in SMK1 transcript levels during middle sporulation show distinct sporulation phenotypes.

摘要

酿酒酵母中的减数分裂发育(孢子形成)的特点是基因表达具有有序模式,孢子形成特异性基因根据其表达时间分为早期、中期、中晚期或晚期。SMK1编码一种孢子形态发生所需的丝裂原活化蛋白激酶,它作为中期孢子形成特异性基因表达。在这里,我们鉴定了调控SMK1转录的顺式作用DNA元件,并对表达模式改变的突变体的表型进行了表征。SMK1启动子包含一个上游激活序列(UASS),它与转录激活因子Abf1p特异性相互作用。早期HOP1启动子和中期SMK1启动子中的Abf1p结合位点在功能上是可互换的,这表明这些元件在它们不同的转录时间中不发挥直接作用。SMK1表达的时间由另一个称为MSE(中期孢子形成元件)的顺式作用DNA序列决定。MSE不仅是中期孢子形成期间SMK1转录激活所必需的,也是营养生长和减数分裂早期其抑制所必需的。此外,SMK1 MSE可以在HOP1启动子的背景下抑制营养期表达,并将HOP1从早期基因转变为中期基因。SMK1的功能并不取决于其作为中期孢子形成特异性基因的严格转录调控。然而,在中期孢子形成期间SMK1转录水平具有不同定量缺陷的启动子突变体表现出不同的孢子形成表型。