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酿酒酵母ANB1基因受血红素的负调控,由ROX1基因产物介导。

Negative regulation of the Saccharomyces cerevisiae ANB1 gene by heme, as mediated by the ROX1 gene product.

作者信息

Lowry C V, Lieber R H

出版信息

Mol Cell Biol. 1986 Dec;6(12):4145-8. doi: 10.1128/mcb.6.12.4145-4148.1986.

Abstract

In Saccharomyces cerevisiae the anaerobic (oxygen-repressed) ANB1 gene and a group of aerobic (oxygen-induced) genes are coordinately regulated by the ROX1 gene. We report here that heme, known as an inducer of aerobic genes, also causes inhibition of ANB1 expression. Thus, in combination with the ROX1 gene product heme has an opposite effect on the expression of anaerobic and aerobic genes. Accumulation of ANB1 mRNA was sharply decreased in anaerobic cells grown in the presence of heme. This effect must operate at the level of transcription since heme also inhibited accumulation of CYC1 mRNA from an ANB1-CYC1 fusion. Heme precursors did not appear to function either as inhibitors or as activators. Oxygen itself also had no effect on transcription of ANB1. Repression by heme cannot be attributed to the respiratory competence conferred by heme since both ANB1 and the aerobic genes tr-1 and CYC1 were regulated normally in [rho 0] mutants. The results are consistent with a classical allosteric coeffector function for heme, although more indirect explanations are tenable. A role for the ROX1 gene product in transcriptional regulation can be inferred from the observation that there was no inhibition of ANB1 expression by heme in rox1 mutants. Judging from this epistasis the rox1 phenotype is not due to a defect in heme production; this would indicate that the ROX1 factor functions by mediating the effect of heme on transcription.

摘要

在酿酒酵母中,厌氧(氧抑制)ANB1基因和一组需氧(氧诱导)基因由ROX1基因协同调控。我们在此报告,已知作为需氧基因诱导剂的血红素,也会抑制ANB1的表达。因此,与ROX1基因产物相结合,血红素对厌氧基因和好氧基因的表达具有相反的作用。在血红素存在下生长的厌氧细胞中,ANB1 mRNA的积累急剧减少。由于血红素也抑制来自ANB1 - CYC1融合体的CYC1 mRNA的积累,这种作用必定在转录水平起作用。血红素前体似乎既不发挥抑制剂的作用,也不发挥激活剂的作用。氧气本身对ANB1的转录也没有影响。血红素的抑制作用不能归因于血红素赋予的呼吸能力,因为在[rho 0]突变体中,ANB1和需氧基因tr - 1及CYC1均受到正常调控。尽管更多间接的解释也是合理的,但这些结果与血红素经典的别构效应器功能一致。从rox1突变体中血红素不抑制ANB1表达这一观察结果可以推断出ROX1基因产物在转录调控中的作用。从这种上位性判断,rox1表型并非由于血红素产生缺陷;这表明ROX1因子通过介导血红素对转录的作用来发挥功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4050/367192/36cea9a7e49a/molcellb00096-0012-a.jpg

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