Natural male hybrid common shrews with a very long chromosomal multivalent at meiosis appear not to be completely sterile

IF 1.8 3区 生物学 Q3 DEVELOPMENTAL BIOLOGY Journal of experimental zoology. Part B, Molecular and developmental evolution Pub Date : 2023-12-07 DOI:10.1002/jez.b.23232
Sergey N. Matveevsky, Oxana L. Kolomiets, Nikolay A. Shchipanov, Svetlana V. Pavlova
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Abstract

Among 36 known chromosomal hybrid zones of the common shrew Sorex araneus, the Moscow–Seliger hybrid zone is of special interest because inter-racial complex heterozygotes (F1 hybrids) produce the longest meiotic configuration, consisting of 11 chromosomes with monobrachial homology (undecavalent or chain-of-eleven: CXI). Different studies suggest that such a multivalent may negatively affect meiotic progression and in general should significantly reduce fertility of hybrids. In this work, by immunocytochemical and electron microscopy methods, we investigated for the first time chromosome synapsis, recombination and meiotic silencing in pachytene spermatocytes of natural inter-racial heterozygous shrew males carrying CXI configurations. Despite some abnormalities detected in spermatocytes, such as associations of chromosomes, stretched centromeres, and the absence of recombination nodules in some arms of the multivalent, a large number of morphologically normal spermatozoa were observed. Possible low stringency of pachytene checkpoints may mean that even very long meiotic configurations do not cause complete sterility of such complex inter-racial heterozygotes.

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在减数分裂时具有很长多价染色体的天然雄性杂交鼩鼱似乎不是完全不育的。
在已知的36个普通鼩染色体杂交区中,莫斯科-塞利格杂交区特别有趣,因为种族间复杂杂合子(F1杂交)产生最长的减数分裂构型,由11条染色体组成,具有单臂同源性(十一链:CXI)。不同的研究表明,这样的多价可能会对减数分裂进程产生负面影响,并且通常会显著降低杂交种的育性。本文采用免疫细胞化学和电镜技术,首次研究了携带CXI构型的自然种间杂合雄性鼩猴粗线精母细胞的染色体突触、重组和减数分裂沉默。尽管在精母细胞中检测到一些异常,如染色体关联,着丝粒拉伸,以及在多价染色体的一些臂中没有重组结节,但仍观察到大量形态正常的精子。粗线蛋白检查点可能的低严格性可能意味着即使很长的减数分裂构型也不会导致这种复杂的种族间杂合子的完全不育。
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来源期刊
CiteScore
4.80
自引率
9.10%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Developmental Evolution is a branch of evolutionary biology that integrates evidence and concepts from developmental biology, phylogenetics, comparative morphology, evolutionary genetics and increasingly also genomics, systems biology as well as synthetic biology to gain an understanding of the structure and evolution of organisms. The Journal of Experimental Zoology -B: Molecular and Developmental Evolution provides a forum where these fields are invited to bring together their insights to further a synthetic understanding of evolution from the molecular through the organismic level. Contributions from all these branches of science are welcome to JEZB. We particularly encourage submissions that apply the tools of genomics, as well as systems and synthetic biology to developmental evolution. At this time the impact of these emerging fields on developmental evolution has not been explored to its fullest extent and for this reason we are eager to foster the relationship of systems and synthetic biology with devo evo.
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