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酵母中的碳分解代谢物阻遏不仅限于葡萄糖。

Carbon Catabolite Repression in Yeast is Not Limited to Glucose.

机构信息

School of Molecular Cell Biology & Biotechnology, Tel Aviv University, Ramat Aviv, 69978, Israel.

出版信息

Sci Rep. 2019 Apr 24;9(1):6491. doi: 10.1038/s41598-019-43032-w.

Abstract

Cells adapt their gene expression and their metabolism in response to a changing environment. Glucose represses expression of genes involved in the catabolism of other carbon sources in a process known as (carbon) catabolite repression. However, the relationships between "poor" carbon sources is less characterized. Here we show that in addition to the well-characterized glucose (and galactose) repression of ADH2 (alcohol dehydrogenase 2, required for efficient utilization of ethanol as a carbon source), ADH2 expression is also inhibited by acetate which is produced during ethanol catabolism. Thus, repressive regulation of gene expression occurs also between "poor" carbon sources. Acetate repression of ADH2 expression is via Haa1, independently from the well-characterized mechanism of AMPK (Snf1) activation of Adr1. The response to extracellular acetate is attenuated when all three acetate transporters (Ady2, Fps1 and Jen1) are deleted, but these deletions do not affect the acetate response resulting from growth with glucose or ethanol as the carbon source. Furthermore, genetic manipulation of the ethanol catabolic pathway affects this response. Together, our results show that acetate is sensed intracellularly and that a hierarchical control of carbon sources exists even for "poor" carbon sources.

摘要

细胞会根据环境变化来调整基因表达和代谢。葡萄糖通过(碳)分解代谢物阻遏作用来抑制其他碳源分解代谢相关基因的表达。然而,对于“较差”碳源之间的关系则了解较少。在这里,我们发现除了众所周知的葡萄糖(和半乳糖)对 ADH2(乙醇作为碳源的有效利用所需的醇脱氢酶 2)的抑制作用外,ADH2 的表达也受到在乙醇分解代谢过程中产生的乙酸的抑制。因此,“较差”碳源之间也存在基因表达的抑制调节。乙酸通过 Haa1 抑制 ADH2 的表达,与 AMPK(Snf1)激活 Adr1 的机制无关。当删除所有三个乙酸转运蛋白(Ady2、Fps1 和 Jen1)时,对外源乙酸的反应会减弱,但这些缺失不会影响葡萄糖或乙醇作为碳源生长时产生的乙酸反应。此外,乙醇分解代谢途径的遗传操作会影响这种反应。综上所述,我们的结果表明,乙酸是在细胞内被感知的,即使对于“较差”碳源,也存在着碳源的分层控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a9/6482301/aef639192e36/41598_2019_43032_Fig1_HTML.jpg

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