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亨廷顿蛋白缺失在黏菌盘基网柄菌中有多种效应。

Deficiency of huntingtin has pleiotropic effects in the social amoeba Dictyostelium discoideum.

机构信息

Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America.

出版信息

PLoS Genet. 2011 Apr;7(4):e1002052. doi: 10.1371/journal.pgen.1002052. Epub 2011 Apr 28.

Abstract

Huntingtin is a large HEAT repeat protein first identified in humans, where a polyglutamine tract expansion near the amino terminus causes a gain-of-function mechanism that leads to selective neuronal loss in Huntington's disease (HD). Genetic evidence in humans and knock-in mouse models suggests that this gain-of-function involves an increase or deregulation of some aspect of huntingtin's normal function(s), which remains poorly understood. As huntingtin shows evolutionary conservation, a powerful approach to discovering its normal biochemical role(s) is to study the effects caused by its deficiency in a model organism with a short life-cycle that comprises both cellular and multicellular developmental stages. To facilitate studies aimed at detailed knowledge of huntingtin's normal function(s), we generated a null mutant of hd, the HD ortholog in Dictyostelium discoideum. Dictyostelium cells lacking endogenous huntingtin were viable but during development did not exhibit the typical polarized morphology of Dictyostelium cells, streamed poorly to form aggregates by accretion rather than chemotaxis, showed disorganized F-actin staining, exhibited extreme sensitivity to hypoosmotic stress, and failed to form EDTA-resistant cell-cell contacts. Surprisingly, chemotactic streaming could be rescued in the presence of the bivalent cations Ca(2+) or Mg(2+) but not pulses of cAMP. Although hd(-) cells completed development, it was delayed and proceeded asynchronously, producing small fruiting bodies with round, defective spores that germinated spontaneously within a glassy sorus. When developed as chimeras with wild-type cells, hd(-) cells failed to populate the pre-spore region of the slug. In Dictyostelium, huntingtin deficiency is compatible with survival of the organism but renders cells sensitive to low osmolarity, which produces pleiotropic cell autonomous defects that affect cAMP signaling and as a consequence development. Thus, Dictyostelium provides a novel haploid organism model for genetic, cell biological, and biochemical studies to delineate the functions of the HD protein.

摘要

亨廷顿蛋白是一种大型热休克蛋白,最初在人类中被发现,其氨基末端附近的多聚谷氨酰胺延伸导致功能获得机制,导致亨廷顿病(HD)中选择性神经元丢失。人类和基因敲入小鼠模型的遗传证据表明,这种功能获得涉及亨廷顿蛋白正常功能的某些方面的增加或失调,但仍知之甚少。由于亨廷顿蛋白具有进化保守性,因此研究其在具有短生命周期的模型生物中的缺乏对其正常生化功能的影响是一种强有力的方法,该模型生物包含细胞和多细胞发育阶段。为了促进对亨廷顿蛋白正常功能的详细研究,我们生成了 Dictyostelium discoideum 中 HD 的同源物 hd 的 null 突变体。缺乏内源性亨廷顿蛋白的 Dictyostelium 细胞具有活力,但在发育过程中没有表现出 Dictyostelium 细胞典型的极化形态,通过 accretion 而不是趋化性较差地流到聚集物中,显示出 F-肌动蛋白染色紊乱,对低渗应激极度敏感,并且无法形成 EDTA 抗性细胞-细胞接触。令人惊讶的是,在存在二价阳离子 Ca(2+)或 Mg(2+)的情况下可以挽救趋化性流,但不能挽救 cAMP 脉冲。尽管 hd(-)细胞完成了发育,但发育过程被延迟并且异步进行,产生了具有圆形、有缺陷的孢子的小子实体,这些孢子在玻璃状子实体中自发萌发。当与野生型细胞形成嵌合体时,hd(-)细胞无法填充 slug 的前孢子区。在 Dictyostelium 中,亨廷顿蛋白缺乏与生物体的存活兼容,但使细胞对低渗透压敏感,这会产生多效性细胞自主缺陷,影响 cAMP 信号传导,并因此影响发育。因此,Dictyostelium 为遗传、细胞生物学和生物化学研究提供了一种新型单倍体生物模型,以描绘 HD 蛋白的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24b1/3084204/6123f9d8bd90/pgen.1002052.g001.jpg

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