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酿酒酵母细胞壁厌氧重塑过程中控制DAN/TIR甘露糖蛋白基因表达的调控机制。

Regulatory mechanisms controlling expression of the DAN/TIR mannoprotein genes during anaerobic remodeling of the cell wall in Saccharomyces cerevisiae.

作者信息

Abramova N E, Cohen B D, Sertil O, Kapoor R, Davies K J, Lowry C V

机构信息

Center for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12203, USA.

出版信息

Genetics. 2001 Mar;157(3):1169-77. doi: 10.1093/genetics/157.3.1169.

Abstract

The DAN/TIR genes of Saccharomyces cerevisiae encode homologous mannoproteins, some of which are essential for anaerobic growth. Expression of these genes is induced during anaerobiosis and in some cases during cold shock. We show that several heme-responsive mechanisms combine to regulate DAN/TIR gene expression. The first mechanism employs two repression factors, Mox1 and Mox2, and an activation factor, Mox4 (for mannoprotein regulation by oxygen). The genes encoding these proteins were identified by selecting for recessive mutants with altered regulation of a dan1::ura3 fusion. MOX4 is identical to UPC2, encoding a binucleate zinc cluster protein controlling expression of an anaerobic sterol transport system. Mox4/Upc2 is required for expression of all the DAN/TIR genes. It appears to act through a consensus sequence termed the AR1 site, as does Mox2. The noninducible mox4Delta allele was epistatic to the constitutive mox1 and mox2 mutations, suggesting that Mox1 and Mox2 modulate activation by Mox4 in a heme-dependent fashion. Mutations in a putative repression domain in Mox4 caused constitutive expression of the DAN/TIR genes, indicating a role for this domain in heme repression. MOX4 expression is induced both in anaerobic and cold-shocked cells, so heme may also regulate DAN/TIR expression through inhibition of expression of MOX4. Indeed, ectopic expression of MOX4 in aerobic cells resulted in partially constitutive expression of DAN1. Heme also regulates expression of some of the DAN/TIR genes through the Rox7 repressor, which also controls expression of the hypoxic gene ANB1. In addition Rox1, another heme-responsive repressor, and the global repressors Tup1 and Ssn6 are also required for full aerobic repression of these genes.

摘要

酿酒酵母的DAN/TIR基因编码同源甘露糖蛋白,其中一些对厌氧生长至关重要。这些基因的表达在厌氧状态下以及某些情况下在冷休克期间被诱导。我们发现几种血红素应答机制共同作用来调节DAN/TIR基因的表达。第一种机制利用两个阻遏因子Mox1和Mox2以及一个激活因子Mox4(用于氧对甘露糖蛋白的调节)。通过筛选dan1::ura3融合基因调控改变的隐性突变体,鉴定出了编码这些蛋白质的基因。MOX4与UPC2相同,编码一种双核锌簇蛋白,控制厌氧甾醇转运系统的表达。Mox4/Upc2是所有DAN/TIR基因表达所必需的。它似乎通过一个称为AR1位点的共有序列起作用,Mox2也是如此。不可诱导的mox4Δ等位基因对组成型的mox1和mox2突变是上位性的,这表明Mox1和Mox2以血红素依赖的方式调节Mox4的激活。Mox4中一个假定的阻遏结构域的突变导致DAN/TIR基因的组成型表达,表明该结构域在血红素阻遏中起作用。MOX4的表达在厌氧和冷休克细胞中均被诱导,因此血红素也可能通过抑制MOX4的表达来调节DAN/TIR的表达。事实上,在需氧细胞中异位表达MOX4导致DAN1的部分组成型表达。血红素还通过Rox7阻遏因子调节一些DAN/TIR基因的表达,Rox7也控制缺氧基因ANB1的表达。此外,另一个血红素应答阻遏因子Rox1以及全局阻遏因子Tup1和Ssn6也是这些基因完全需氧阻遏所必需的。

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