The yeast mRNA-binding protein Cth2 post-transcriptionally modulates ergosterol biosynthesis in response to iron deficiency

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et Biophysica Acta-Gene Regulatory Mechanisms Pub Date : 2023-09-01 DOI:10.1016/j.bbagrm.2023.194959
Tania Jordá , Nicolas Rozès , María Teresa Martínez-Pastor , Sergi Puig
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Abstract

Sterol synthesis is an iron-dependent metabolic pathway in eukaryotes. Consequently, fungal ergosterol biosynthesis (ERG) is down-regulated in response to iron deficiency. In this report, we show that, upon iron limitation or overexpression of the iron-regulated mRNA-binding protein Cth2, the yeast Saccharomyces cerevisiae down-regulates the three initial enzymatic steps of ergosterol synthesis (ERG1, ERG7 and ERG11). Mechanistically, we show that Cth2 protein limits the translation and promotes the decrease in the mRNA levels of these specific ERG genes, which contain consensus Cth2-binding sites defined as AU-rich elements (AREs). Thus, expression of CTH2 leads to the accumulation of initial sterol intermediates, such as squalene, and to the drop of ergosterol levels. Changes in CTH2 expression levels disturb the response of yeast cells to stresses related to membrane integrity such as high ethanol and sorbitol concentrations. Therefore, CTH2 should be considered as a critical regulatory factor of ergosterol biosynthesis during iron deficiency.

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酵母mrna结合蛋白Cth2转录后调节麦角甾醇的生物合成以应对缺铁
甾醇合成是真核生物中依赖铁的代谢途径。因此,真菌麦角甾醇生物合成(ERG)在铁缺乏的情况下下调。在本报告中,我们发现,当铁限制或过表达铁调控的mrna结合蛋白Cth2时,酵母酵母下调麦角甾醇合成的三个初始酶促步骤(ERG1, ERG7和ERG11)。在机制上,我们发现Cth2蛋白限制了翻译并促进了这些特定ERG基因mRNA水平的降低,这些基因含有共识的Cth2结合位点,被定义为富au元件(AREs)。因此,CTH2的表达导致初始固醇中间体(如角鲨烯)的积累,并导致麦角甾醇水平的下降。CTH2表达水平的变化扰乱了酵母细胞对与膜完整性相关的应激(如高乙醇和山梨醇浓度)的反应。因此,CTH2应被认为是缺铁时麦角甾醇生物合成的关键调控因子。
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来源期刊
CiteScore
9.20
自引率
2.10%
发文量
63
审稿时长
44 days
期刊介绍: BBA Gene Regulatory Mechanisms includes reports that describe novel insights into mechanisms of transcriptional, post-transcriptional and translational gene regulation. Special emphasis is placed on papers that identify epigenetic mechanisms of gene regulation, including chromatin, modification, and remodeling. This section also encompasses mechanistic studies of regulatory proteins and protein complexes; regulatory or mechanistic aspects of RNA processing; regulation of expression by small RNAs; genomic analysis of gene expression patterns; and modeling of gene regulatory pathways. Papers describing gene promoters, enhancers, silencers or other regulatory DNA regions must incorporate significant functions studies.
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