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Mpt5p, a Stress Tolerance- and Lifespan-Promoting PUF Protein in Saccharomyces cerevisiae, Acts Upstream of the Cell Wall Integrity Pathway▿

机译:Mpt5p是酿酒酵母中一种耐压力和延长寿命的PUF蛋白,在细胞壁完整性通路的上游起作用▿

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摘要

Pumilio family (PUF) proteins affect specific genes by binding to, and inhibiting the translation or stability of, their transcripts. The PUF domain is required and sufficient for this function. One Saccharomyces cerevisiae PUF protein, Mpt5p (also called Puf5p or Uth4p), promotes stress tolerance and replicative life span (the maximum number of doublings a mother cell can undergo before entering into senescence) by an unknown mechanism thought to partly overlap with, but to be independent of, the cell wall integrity (CWI) pathway. Here, we found that mpt5Δ mutants also display a short chronological life span (the time cells stay alive in saturated cultures in synthetic medium), a defect that is suppressed by activation of CWI signaling. We found that Mpt5p is an upstream activator of the CWI pathway: mpt5Δ mutants display the appropriate phenotypes and genetic interactions, display low basal activity of the pathway, and are defective in activation of the pathway upon thermal stress. A set of mRNAs that specifically bind to Mpt5p was recently reported. One such putative target, LRG1, encodes a GTPase-activating protein for Rho1p that directly links Mpt5p to CWI signaling: Lrg1p inhibits CWI signaling, LRG1 mRNA contains a consensus Mpt5p-binding site in its putative 3′ untranslated region, loss of Lrg1p suppresses the temperature sensitivity and CWI signaling defects of mpt5Δ mutants, and LRG1 mRNA abundance is inhibited by Mpt5p. We conclude that Mpt5p is required for normal replicative and chronological life spans and that the CWI pathway is a key and direct downstream target of this PUF protein.
机译:Pumilio家族(PUF)蛋白通过与转录物结合并抑制其转录或稳定性来影响特定基因。 PUF域是必需的,并且对于此功能而言已足够。一种酿酒酵母PUF蛋白Mpt5p(也称为Puf5p或Uth4p)可通过一种未知的机制来提高压力耐受性和复制寿命(母细胞进入衰老之前可经历的最大倍增次数),该机制被认为部分重叠,但独立于细胞壁完整性(CWI)途径。在这里,我们发现mpt5Δ突变体还显示出较短的时间寿命(时间细胞在合成培养基中的饱和培养物中存活),该缺陷可通过激活CWI信号来抑制。我们发现Mpt5p是CWI途径的上游激活剂:mpt5Δ突变体显示适当的表型和遗传相互作用,显示该途径的低基础活性,并且在热胁迫下在激活该途径方面存在缺陷。最近报道了一组与Mpt5p特异性结合的mRNA。一种这样的推定靶标LRG1编码Rho1p的GTPase激活蛋白,该蛋白直接将Mpt5p连接到CWI信号传导:Lrg1p抑制CWI信号传导,LRG1 mRNA在其推定的3'非翻译区中包含一个共有Mpt5p结合位点,Lrg1p的缺失抑制了CWI信号传导。 Mpt5p突变体的温度敏感性和CWI信号缺陷,以及LRG1 mRNA的丰度受到Mpt5p的抑制。我们得出结论,正常复制和按时间顺序排列的生命周期需要Mpt5p,并且CWI途径是该PUF蛋白的关键和直接下游靶标。

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