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小须鲸重组调控因子 PRDM9 的进化。

Evolution of the recombination regulator PRDM9 in minke whales.

机构信息

Department Evolutionary Genetics, Research Group Meiotic Recombination and Genome Instability, Max Planck Institute for Evolutionary Biology, August-Thienemann Str. 2, D-24306, Plön, Germany.

Department of Zoology, University of Cambridge, Cambridge, UK.

出版信息

BMC Genomics. 2022 Mar 16;23(1):212. doi: 10.1186/s12864-022-08305-1.

Abstract

BACKGROUND

PRDM9 is a key regulator of meiotic recombination in most metazoans, responsible for reshuffling parental genomes. During meiosis, the PRDM9 protein recognizes and binds specific target motifs via its array of CH zinc-fingers encoded by a rapidly evolving minisatellite. The gene coding for PRDM9 is the only speciation gene identified in vertebrates to date and shows high variation, particularly in the DNA-recognizing positions of the zinc-finger array, within and between species. Across all vertebrate genomes studied for PRDM9 evolution, only one genome lacks variability between repeat types - that of the North Pacific minke whale. This study aims to understand the evolution and diversity of Prdm9 in minke whales, which display the most unusual genome reference allele of Prdm9 so far discovered in mammals.

RESULTS

Minke whales possess all the features characteristic of PRDM9-directed recombination, including complete KRAB, SSXRD and SET domains and a rapidly evolving array of CH-type-Zincfingers (ZnF) with evidence of rapid evolution, particularly at DNA-recognizing positions that evolve under positive diversifying selection. Seventeen novel PRDM9 variants were identified within the Antarctic minke whale species, plus a single distinct PRDM9 variant in Common minke whales - shared across North Atlantic and North Pacific minke whale subspecies boundaries.

CONCLUSION

The PRDM9 ZnF array evolves rapidly, in minke whales, with at least one DNA-recognizing position under positive selection. Extensive PRDM9 diversity is observed, particularly in the Antarctic in minke whales. Common minke whales shared a specific Prdm9 allele across subspecies boundaries, suggesting incomplete speciation by the mechanisms associated with PRDM9 hybrid sterility.

摘要

背景

PRDM9 是大多数后生动物减数分裂重组的关键调节因子,负责重排亲本基因组。在减数分裂过程中,PRDM9 蛋白通过其由快速进化的小卫星编码的 CH 锌指阵列识别和结合特定的靶标基序。到目前为止,编码 PRDM9 的基因是在脊椎动物中鉴定出的唯一物种形成基因,表现出高度的变异性,特别是在锌指阵列的 DNA 识别位置,在种内和种间都有很大的变化。在所有研究 PRDM9 进化的脊椎动物基因组中,只有一种基因组缺乏重复类型之间的可变性——北太平洋小须鲸的基因组。本研究旨在了解小须鲸中 Prdm9 的进化和多样性,小须鲸表现出迄今为止在哺乳动物中发现的最不寻常的基因组参考等位基因。

结果

小须鲸具有 PRDM9 指导重组的所有特征,包括完整的 KRAB、SSXRD 和 SET 结构域,以及一个快速进化的 CH 型锌指(ZnF)阵列,具有快速进化的证据,特别是在 DNA 识别位置,这些位置在正选择下进化。在南极小须鲸种内鉴定出了 17 种新的 PRDM9 变体,以及在普通小须鲸中存在一种独特的 PRDM9 变体——在北大西洋和北太平洋小须鲸亚种边界内共享。

结论

在小须鲸中,PRDM9 ZnF 阵列快速进化,至少有一个 DNA 识别位置受到正选择的影响。观察到广泛的 PRDM9 多样性,特别是在南极小须鲸中。普通小须鲸在亚种边界内共享一个特定的 Prdm9 等位基因,这表明种间隔离机制不完全,与 PRDM9 杂种不育有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d074/8925151/f3464513b669/12864_2022_8305_Fig1_HTML.jpg

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