首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Expression of genes encoding peroxisomal proteins in Saccharomyces cerevisiae is regulated by different circuits of transcriptional control
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Expression of genes encoding peroxisomal proteins in Saccharomyces cerevisiae is regulated by different circuits of transcriptional control

机译:酿酒酵母中编码过氧化物酶体蛋白的基因的表达受转录控制的不同途径调控

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In Saccharomyces cerevisiae induction of the FOX3 gene, encoding peroxisomal 3-oxoacyl-CoA thiolase, by growth on oleate as sole carbon source, is exerted via the cis-acting DNA element designated oleate response element (ORE) (Einerhand et al. (1991) Eur. J. Biochem. 200, 113-122). The transcription factor(s) binding to this upstream activation site (UAS) are still unknown, however. Induction of another peroxisomal enzyme, citrate synthase (CIT2) is dependent on the products of two genes called RTG1 and RTG2 (Liao and Butow (1993) Cell 72, 61-71). In the present study we have investigated whether RTG1 controls other genes coding for peroxisomal proteins, and whether such control takes place via the ORE. A number of genes coding for a variety of peroxisomal proteins such as: thiolase and catalase (peroxisomal matrix proteins), PAS3p (a peroxisomal membrane protein) and PAS10p (a protein involved in the import of peroxisomal proteins) were studied in their response to RTG1. Although the RTG1 and 2 products proved to be required for the increase in number and volume of peroxisomes upon induction by oleate, the single promoter output of the chosen set of genes remained practically unchanged in a rtg1 mutant strain. In addition gel retardation experiments indicated that RTG1 does not bind to the ORE. The behavior of genes coding for the various proteins also varied during repression, derepression and induction, indicating that probably a number of proteins are involved in tuning the output of each gene to cellular demand.
机译:在酿酒酵母中,通过在油酸盐上生长作为唯一碳源,通过编码油酸反应元件(ORE)来诱导编码过氧化物酶体3-氧代酰基-CoA硫解酶的FOX3基因(Einerhand等(1991)。 Eur.J.Biochem.200,113-122)。然而,与该上游激活位点(UAS)结合的转录因子仍然未知。另一过氧化物酶体酶柠檬酸合酶(CIT2)的诱导取决于称为RTG1和RTG2的两个基因的产物(Liao and Butow(1993)Cell 72,61-71)。在本研究中,我们研究了RTG1是否控制其他编码过氧化物酶体蛋白的基因,以及这种控制是否通过ORE进行。研究了编码多种过氧化物酶体蛋白的许多基因,例如硫解酶和过氧化氢酶(过氧化物酶体基质蛋白),PAS3p(过氧化物酶体膜蛋白)和PAS10p(过氧化物酶体蛋白的进口蛋白)对RTG1的反应。 。尽管RTG1和2产物被证明是油酸诱导过氧化物酶体数量和体积增加所必需的,但所选基因组的单启动子输出在rtg1突变菌株中实际上保持不变。另外,凝胶阻滞实验表明RTG1不与ORE结合。编码各种蛋白质的基因的行为在阻抑,抑制和诱导过程中也发生变化,这表明可能在调节每种基因的输出以适应细胞需求方面涉及多种蛋白质。

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