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环境响应性朊病毒导致酵母细胞发生可遗传的重塑。

Heritable remodeling of yeast multicellularity by an environmentally responsive prion.

机构信息

Department of Biochemistry, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, USA.

出版信息

Cell. 2013 Mar 28;153(1):153-65. doi: 10.1016/j.cell.2013.02.026.

Abstract

Prion proteins undergo self-sustaining conformational conversions that heritably alter their activities. Many of these proteins operate at pivotal positions in determining how genotype is translated into phenotype. But the breadth of prion influences on biology and their evolutionary significance are just beginning to be explored. We report that a prion formed by the Mot3 transcription factor, [MOT3(+)], governs the acquisition of facultative multicellularity in the budding yeast Saccharomyces cerevisiae. The traits governed by [MOT3(+)] involved both gains and losses of Mot3 regulatory activity. [MOT3(+)]-dependent expression of FLO11, a major determinant of cell-cell adhesion, produced diverse lineage-specific multicellular phenotypes in response to nutrient deprivation. The prions themselves were induced by ethanol and eliminated by hypoxia-conditions that occur sequentially in the natural respiro-fermentative cycles of yeast populations. These data demonstrate that prions can act as environmentally responsive molecular determinants of multicellularity and contribute to the natural morphological diversity of budding yeast.

摘要

朊病毒蛋白会经历自我维持的构象转换,从而遗传地改变它们的活性。这些蛋白质中的许多都在决定基因型如何转化为表型方面起着关键作用。但是,朊病毒对生物学的广泛影响及其进化意义才刚刚开始被探索。我们报告说,由转录因子 Mot3 形成的朊病毒 [MOT3(+)] 控制着出芽酵母酿酒酵母中兼性多细胞性的获得。[MOT3(+)] 控制的特性既涉及 Mot3 调节活性的获得,也涉及 Mot3 调节活性的丧失。FLO11 的表达依赖于 [MOT3(+)],FLO11 是细胞间黏附的主要决定因素,在营养缺乏时会产生各种谱系特异性的多细胞表型。朊病毒本身是由乙醇诱导的,由缺氧消除的,而缺氧条件是在酵母群体的自然呼吸发酵循环中顺序发生的。这些数据表明,朊病毒可以作为环境响应的多细胞性分子决定因素,并有助于出芽酵母的自然形态多样性。

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本文引用的文献

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Does the central dogma still stand?中心法则是否仍然成立?
Biol Direct. 2012 Aug 23;7:27. doi: 10.1186/1745-6150-7-27.
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Experimental evolution of multicellularity.实验进化中的多细胞性。
Proc Natl Acad Sci U S A. 2012 Jan 31;109(5):1595-600. doi: 10.1073/pnas.1115323109. Epub 2012 Jan 17.

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