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鱼精蛋白敲低模拟了[具体内容缺失]中[具体内容缺失]的功能。

A Protamine Knockdown Mimics the Function of in .

作者信息

Gingell Luke F, McLean Janna R

机构信息

Department of Biology and Chemistry, Bethel University, Mishawaka, Indiana, 46545.

Department of Biology and Chemistry, Bethel University, Mishawaka, Indiana, 46545

出版信息

G3 (Bethesda). 2020 Jun 1;10(6):2111-2115. doi: 10.1534/g3.120.401307.

Abstract

() is an autosomal meiotic drive system found worldwide in natural populations of This gene complex induces the preferential and nearly exclusive transmission of the chromosome in / males. This selfish propagation occurs through the interplay of the locus, its enhancers and the locus during spermatid development. The key distorter locus, , encodes a truncated but enzymatically active RanGAP (RanGTPase-activating protein), a key nuclear transport factor in the Ran signaling pathway. When encoded by , RanGAP is mislocalized to the nucleus interior, which then traps Ran inside the nucleus and disrupts nuclear import. As a result of this aberrant nuclear transport, a process known as the histone-to-protamine transition that is required for proper spermatid condensation fails to occur in / males. In this process, sperm-specific protamine proteins enter the spermatid nucleus and replace the formerly chromatin-complexed histones. Previously, we have shown that mutations affecting nuclear import and export can enhance distortion in an background, thus verifying that a defect in nuclear transport is responsible for the unequal transmission of chromosomes. Herein, we show that specifically reducing protamines induces distortion in an background, verifying that protamines are transported via the RanGAP/GEF pathway and indicating that plays a significant and unique role in the process of distortion.

摘要

()是一种常染色体减数分裂驱动系统,在全世界的自然种群中均有发现。该基因复合体在 / 雄性个体中诱导染色体的优先且几乎完全的传递。这种自私的繁殖通过精子细胞发育过程中位点、其增强子和位点之间的相互作用而发生。关键的扭曲位点编码一种截短但具有酶活性的RanGAP(Ran鸟苷三磷酸酶激活蛋白),它是Ran信号通路中的关键核转运因子。当由编码时,RanGAP会错误定位于细胞核内部,进而将Ran困在细胞核内并破坏核输入。由于这种异常的核转运,精子细胞正常浓缩所需的组蛋白到鱼精蛋白的转变过程在 / 雄性个体中无法发生。在这个过程中,精子特异性鱼精蛋白进入精子细胞核并取代先前与染色质结合的组蛋白。此前,我们已经表明影响核输入和输出的突变可以在背景中增强扭曲,从而证实核转运缺陷是染色体不平等传递的原因。在此,我们表明特异性降低鱼精蛋白会在背景中诱导扭曲,证实鱼精蛋白通过RanGAP/GEF途径转运,并表明在扭曲过程中发挥着重要且独特的作用。

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