Fertility Cost (or Sometimes a Lack of It) in Relation to Heterozygosity for Robertsonian Rearrangements in Mammals: A Review.

IF 1.3 4区 生物学 Q4 CELL BIOLOGY
Jeremy B Searle, Jonathan J Hughes
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引用次数: 0

Abstract

Background: Robertsonian (Rb) chromosomal rearrangements are very common in mammals and are the primary basis of chromosome number variation between species. The fertility of heterozygotes has particular significance in understanding the mode of fixation of Rb rearrangements, and could have a role in the attainment of reproductive isolation by chromosomally differentiated species.

Summary: Here we survey available data on fertility of Rb heterozygotes in mammals, comparing with homozygotes, and considering effects on litter size, frequencies of anaphase I nondisjunction, germ cell death and pachytene features associated with that germ cell death. We consider both simple heterozygotes which form trivalent configurations at meiosis I and complex heterozygotes which form longer configurations due to heterozygosity for different chromosomes with monobrachial homology. Two species have a particularly wide variety of Rb heterozygotes and have been well studied: the house mouse (the western subspecies) and the common shrew. The overall data confirm that heterozygosity for a single Rb metacentric may be associated with near-normal fertility in mammals, though not in every instance. Usually infertility is not going to be a substantial hindrance to fixation of Rb fusions or fissions. Nor is infertility in simple heterozygotes for one or a few Rb metacentrics on its own likely to promote reproductive isolation. However, simple heterozygotes forming many meiotic trivalents and complex heterozygotes forming long meiotic configurations may suffer substantial infertility or sterility. Even so, heterozygous house mice and common shrews forming the very longest meiotic chains and rings may produce some young. We discuss the implications of these findings with regards the role of Rb rearrangements in speciation.

Key messages: Infertility due to Rb heterozygosity on its own may rarely hinder fixation of Rb rearrangements nor be sufficient to cause a complete interruption to gene flow between hybridizing chromosomal forms. However, this does not rule out a role for Rb rearrangements in speciation. Reinforcement is possible, and Rb rearrangements have the potential to act in synergy with genic incompatibilities to promote reproductive isolation. There can also be the contrary process of despeciation. Natural selection may respond in various ways to a given degree of infertility.

哺乳动物罗伯逊重排的杂合性与生育成本(或缺乏生育成本)的关系:综述。
背景:罗伯逊(Rb)染色体重排在哺乳动物中非常常见,是物种间染色体数目变异的主要基础。杂合子的育性对理解Rb重排的固定模式具有特殊意义,并可能在染色体分化物种实现生殖隔离方面发挥作用。摘要:本研究调查了哺乳动物Rb杂合子的育性数据,与纯合子进行了比较,并考虑了对产仔数、后期I不分离频率、生殖细胞死亡和与生殖细胞死亡相关的粗线特征的影响。我们考虑了在减数分裂I时形成三价构型的简单杂合子和由于具有单臂同源性的不同染色体的杂合性而形成较长构型的复杂杂合子。有两种物种的Rb杂合子种类特别多,已经得到了很好的研究:家鼠(西部亚种)和普通鼩鼱。总体数据证实,单个Rb稳中心的杂合性可能与哺乳动物接近正常的生育力有关;虽然不是每一个例子都是这样。通常不孕症不会成为Rb融合或分裂固定的实质性障碍。一个或几个Rb稳中心的简单杂合子本身的不育也不可能促进生殖隔离。然而,形成许多减数分裂三价的简单杂合子和形成长减数分裂构型的复杂杂合子可能遭受严重的不育或不育。即便如此,形成最长减数分裂链和环的杂合子家鼠和普通鼩鼱可能会产生一些后代。我们就Rb重排在物种形成中的作用讨论了这些发现的含义。关键信息:Rb杂合性本身导致的不育很少会阻碍Rb重排的固定,也不足以导致杂交染色体形式之间的基因流动完全中断。然而,这并不排除Rb重排在物种形成中的作用。强化是可能的,Rb重排可能与基因不相容协同作用,促进生殖隔离。也可能有相反的鄙视过程。自然选择可能以各种方式对一定程度的不孕症作出反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cytogenetic and Genome Research
Cytogenetic and Genome Research 生物-细胞生物学
CiteScore
3.10
自引率
5.90%
发文量
25
审稿时长
1 months
期刊介绍: During the last decades, ''Cytogenetic and Genome Research'' has been the leading forum for original reports and reviews in human and animal cytogenetics, including molecular, clinical and comparative cytogenetics. In recent years, most of its papers have centered on genome research, including gene cloning and sequencing, gene mapping, gene regulation and expression, cancer genetics, comparative genetics, gene linkage and related areas. The journal also publishes key papers on chromosome aberrations in somatic, meiotic and malignant cells. Its scope has expanded to include studies on invertebrate and plant cytogenetics and genomics. Also featured are the vast majority of the reports of the International Workshops on Human Chromosome Mapping, the reports of international human and animal chromosome nomenclature committees, and proceedings of the American and European cytogenetic conferences and other events. In addition to regular issues, the journal has been publishing since 2002 a series of topical issues on a broad variety of themes from cytogenetic and genome research.
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