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普通鼩鼱(Sorex araneus L.,鼩鼱科,真盲缺目)两个染色体种族雄性杂种中的染色体联会与重组

Chromosome Synapsis and Recombination in Male Hybrids between Two Chromosome Races of the Common Shrew (Sorex araneus L., Soricidae, Eulipotyphla).

作者信息

Belonogova Nadezhda M, Polyakov Andrei V, Karamysheva Tatyana V, Torgasheva Anna A, Searle Jeremy B, Borodin Pavel M

机构信息

Institute of Cytology and Genetics, Russian Academy of Sciences, Siberian Department, Novosibirsk 630090, Russia.

Novosibirsk State University, Department of Cytology and Genetics, Novosibirsk 630090, Russia.

出版信息

Genes (Basel). 2017 Oct 20;8(10):282. doi: 10.3390/genes8100282.

Abstract

Hybrid zones between chromosome races of the common shrew () provide exceptional models to study the potential role of chromosome rearrangements in the initial steps of speciation. The Novosibirsk and Tomsk races differ by a series of Robertsonian fusions with monobrachial homology. They form a narrow hybrid zone and generate hybrids with both simple (chain of three chromosomes) and complex (chain of eight or nine) synaptic configurations. Using immunolocalisation of the meiotic proteins, we examined chromosome pairing and recombination in males from the hybrid zone. Homozygotes and simple heterozygotes for Robertsonian fusions showed a low frequency of synaptic aberrations (<10%). The carriers of complex synaptic configurations showed multiple pairing abnormalities, which might lead to reduced fertility. The recombination frequency in the proximal regions of most chromosomes of all karyotypes was much lower than in the other regions. The strong suppression of recombination in the pericentromeric regions and co-segregation of race specific chromosomes involved in the long chains would be expected to lead to linkage disequilibrium between genes located there. Genic differentiation, together with the high frequency of pairing aberrations in male carriers of the long chains, might contribute to maintenance of the narrow hybrid zone.

摘要

普通鼩鼱()染色体族之间的杂交带为研究染色体重排在物种形成初始阶段的潜在作用提供了绝佳模型。新西伯利亚族和托木斯克族因一系列具有单臂同源性的罗伯逊融合而有所不同。它们形成了一个狭窄的杂交带,并产生具有简单(三条染色体的链)和复杂(八条或九条染色体的链)联会构型的杂种。利用减数分裂蛋白的免疫定位,我们研究了杂交带雄性个体的染色体配对和重组情况。罗伯逊融合的纯合子和简单杂合子显示出较低的联会畸变频率(<10%)。具有复杂联会构型的个体表现出多种配对异常,这可能导致生育力下降。所有核型的大多数染色体近端区域的重组频率远低于其他区域。着丝粒周围区域重组的强烈抑制以及长链中涉及的种族特异性染色体的共分离预计会导致位于那里的基因之间的连锁不平衡。基因分化,以及长链雄性携带者中高频率的配对畸变,可能有助于维持狭窄的杂交带。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e402/5664132/c210e95eda13/genes-08-00282-g001.jpg

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