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全着丝粒染色体可能无法阻止莎草科中的着丝粒驱动。

Holocentric Chromosomes Probably Do Not Prevent Centromere Drive in Cyperaceae.

作者信息

Krátká Marie, Šmerda Jakub, Lojdová Kateřina, Bureš Petr, Zedek František

机构信息

Department of Botany and Zoology, Faculty of Science, Masaryk University, Brno, Czechia.

出版信息

Front Plant Sci. 2021 Feb 19;12:642661. doi: 10.3389/fpls.2021.642661. eCollection 2021.

Abstract

Centromere drive model describes an evolutionary process initiated by centromeric repeats expansion, which leads to the recruitment of excess kinetochore proteins and consequent preferential segregation of an expanded centromere to the egg during female asymmetric meiosis. In response to these selfish centromeres, the histone protein CenH3, which recruits kinetochore components, adaptively evolves to restore chromosomal parity and counter the detrimental effects of centromere drive. Holocentric chromosomes, whose kinetochores are assembled along entire chromosomes, have been hypothesized to prevent expanded centromeres from acquiring a selective advantage and initiating centromere drive. In such a case, CenH3 would be subjected to less frequent or no adaptive evolution. Using codon substitution models, we analyzed 36 CenH3 sequences from 35 species of the holocentric family Cyperaceae. We found 10 positively selected codons in the CenH3 gene [six codons in the N-terminus and four in the histone fold domain (HFD)] and six branches of its phylogeny along which the positive selection occurred. One of the positively selected codons was found in the centromere targeting domain (CATD) that directly interacts with DNA and its mutations may be important in centromere drive suppression. The frequency of these positive selection events was comparable to the frequency of positive selection in monocentric clades with asymmetric female meiosis. Taken together, these results suggest that preventing centromere drive is not the primary adaptive role of holocentric chromosomes, and their ability to suppress it likely depends on their kinetochore structure in meiosis.

摘要

着丝粒驱动模型描述了一个由着丝粒重复序列扩增引发的进化过程,这会导致过多动粒蛋白的募集,进而在雌性不对称减数分裂期间使扩增的着丝粒优先分离到卵细胞中。作为对这些自私着丝粒的响应,招募动粒成分的组蛋白CenH3会适应性进化,以恢复染色体平衡并对抗着丝粒驱动的有害影响。全着丝粒染色体的动粒沿着整条染色体组装,据推测,这种染色体可以防止扩增的着丝粒获得选择优势并启动着丝粒驱动。在这种情况下,CenH3的适应性进化频率会更低或根本不会发生适应性进化。我们使用密码子替换模型,分析了来自莎草科全着丝粒家族35个物种的36条CenH3序列。我们在CenH3基因中发现了10个正选择密码子(N端有6个密码子,组蛋白折叠域有4个),以及系统发育树中发生正选择的6个分支。其中一个正选择密码子位于着丝粒靶向结构域(CATD),该结构域直接与DNA相互作用,其突变可能在抑制着丝粒驱动方面具有重要作用。这些正选择事件的频率与具有不对称雌性减数分裂的单着丝粒分支中的正选择频率相当。综上所述,这些结果表明,防止着丝粒驱动并非全着丝粒染色体的主要适应性作用,它们抑制着丝粒驱动的能力可能取决于其在减数分裂中的动粒结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e9/7933567/c3e74d102201/fpls-12-642661-g001.jpg

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