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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.

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。

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