Cell Biology of Cheating-Transmission of Centromeres and Other Selfish Elements Through Asymmetric Meiosis.

Lukáš Chmátal, Richard M Schultz, Ben E Black, Michael A Lampson
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引用次数: 21

Abstract

Mendel's First Law of Genetics states that a pair of alleles segregates randomly during meiosis so that one copy of each is represented equally in gametes. Whereas male meiosis produces four equal sperm, in female meiosis only one cell, the egg, survives, and the others degenerate. Meiotic drive is a process in which a selfish DNA element exploits female meiotic asymmetry and segregates preferentially to the egg in violation of Mendel's First Law, thereby increasing its transmission to the offspring and frequency in a population. In principle, the selfish element can consist either of a centromere that increases its transmission via an altered kinetochore connection to the meiotic spindle or a centromere-like element that somehow bypasses the kinetochore altogether in doing so. There are now examples from eukaryotic model systems for both types of meiotic drive. Although meiotic drive has profound evolutionary consequences across many species, relatively little is known about the underlying mechanisms. We discuss examples in various systems and open questions about the underlying cell biology, and propose a mechanism to explain biased segregation in mammalian female meiosis.

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不对称减数分裂中着丝粒和其他自私因子的欺骗传递的细胞生物学。
孟德尔的遗传第一定律指出,一对等位基因在减数分裂过程中随机分离,因此每个等位基因的一个拷贝在配子中是平等的。男性减数分裂产生四个相等的精子,而在女性减数分裂中,只有一个细胞,即卵子,存活下来,而其他细胞则退化。减数分裂驱动是一个过程,在这个过程中,一个自私的DNA元素利用女性减数分裂的不对称性,违反孟德尔第一定律,优先与卵子分离,从而增加其传递给后代和在群体中的频率。从原理上讲,自私元件可以是通过改变着丝粒与减数分裂纺锤体的连接来增加其传输的着丝粒,也可以是通过某种方式绕过着丝粒来增加传输的着丝粒样元件。现在真核生物模型系统中有两种减数分裂驱动的例子。尽管减数分裂驱动在许多物种中具有深远的进化影响,但对其潜在机制的了解相对较少。我们讨论了各种系统中的例子和关于潜在细胞生物学的开放问题,并提出了一种解释哺乳动物雌性减数分裂中偏隔离的机制。
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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
7
期刊介绍: Molecular biology has been providing an overwhelming amount of data on the structural components and molecular machineries of the cell and its organelles and the complexity of intra- and intercellular communication. The molecular basis of hereditary and acquired diseases is beginning to be unravelled, and profound new insights into development and evolutionary biology have been gained from molecular approaches. Progress in Molecular and Subcellular Biology summarises the most recent developments in this fascinating area of biology.
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