Detecting coevolution of positively selected in turtles sperm-egg fusion proteins

IF 2.6 Q2 Medicine Mechanisms of Development Pub Date : 2019-04-01 DOI:10.1016/j.mod.2019.02.001
Jinxiu Dong, Hui Jiang, Lei Xiong, Jiawei Zan, Jianjun Liu, Mengli Yang, Kai Zheng, Ziming Wang, Liuwang Nie
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引用次数: 4

Abstract

Physically interacting sperm-egg proteins have been identified using gene-modified animals in some mammal species. Three proteins are essential for sperm-egg binding: Izumo1 on the sperm surface, and JUNO and CD9 on the egg surface. Most proteins linked to reproductive function evolve rapidly among species by positive selection, and have correlated evolutionary rates to compensate for changes on both the sperm and egg. Up to now, interactions between sperm and egg proteins have not been identified in non-mammalian vertebrates, such as turtles that have interspecific hybrids that can produce surviving F1 generations. To explore the potential physical interactions of sperm-egg proteins in turtle species, the coding region of Izumo1, JUNO, and CD9 homologous genes (named Tu-Izumo1, Tu-JUNO, and Tu-CD9) in six turtle species (Mauremys reevesii, M. mutica, M. sinensis, Cistoclemmys flavomarginata, Platysternon megacephalum and Chrysemys picta bellii) were identified, amplified, and sequenced, and tissue-specific expression was analyzed in M. reevesii. We constructed phylogenetic trees and analyzed the signatures of coevolution between sperm-egg protein pairs using MirrorTree Server and linear regression methods. The results showed that Tu-Izumo1, Tu-JUNO, and Tu-CD9 proteins have correlated evolutionary rates, and that the area where Tu-Izumo1 interacts with Tu-JUNO has only one positive selection site in some turtle species. These results suggest there is a potential interaction between Tu-Izumo1 and Tu-JUNO among turtles that can interbreed, and that a significantly lower positive selection in the interaction region may be one of the reasons why turtle hybrids are so common. Further studies are required to uncover Tu-Izumo1, Tu-JUNO and Tu-CD9 protein biological functions during gamete fusion.

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检测海龟精卵融合蛋白正选择的协同进化
在一些哺乳动物物种中,已经用基因修饰的动物鉴定出了物理相互作用的精卵蛋白。三种蛋白质对精子与卵子的结合至关重要:精子表面的Izumo1,卵子表面的JUNO和CD9。大多数与生殖功能相关的蛋白质通过正向选择在物种中迅速进化,并具有相关的进化速率来补偿精子和卵子的变化。到目前为止,精子和卵子蛋白之间的相互作用还没有在非哺乳动物脊椎动物中被发现,比如海龟,它们有种间杂交,可以产生存活的F1代。为探索龟种间精卵蛋白的潜在物理相互作用,对6种龟种(毛龟、毛龟、中华龟、黄颡鱼、大头Platysternon megacephalum和黄颡鱼Chrysemys picta belli)的Izumo1、JUNO和CD9同源基因(Tu-Izumo1、Tu-JUNO和Tu-CD9)进行了鉴定、扩增和测序,并对其组织特异性表达进行了分析。利用MirrorTree Server和线性回归方法构建了系统进化树,分析了精卵蛋白对的共同进化特征。结果表明,Tu-Izumo1、Tu-JUNO和Tu-CD9蛋白具有相关的进化速率,并且在某些海龟物种中,Tu-Izumo1与Tu-JUNO相互作用的区域只有一个阳性选择位点。这些结果表明,在可以杂交的海龟中,Tu-Izumo1和Tu-JUNO之间存在潜在的相互作用,而相互作用区明显较低的正选择可能是海龟杂交如此普遍的原因之一。需要进一步的研究来揭示Tu-Izumo1、Tu-JUNO和Tu-CD9蛋白在配子融合过程中的生物学功能。
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来源期刊
Mechanisms of Development
Mechanisms of Development 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
12.4 weeks
期刊介绍: Mechanisms of Development is an international journal covering the areas of cell biology and developmental biology. In addition to publishing work at the interphase of these two disciplines, we also publish work that is purely cell biology as well as classical developmental biology. Mechanisms of Development will consider papers in any area of cell biology or developmental biology, in any model system like animals and plants, using a variety of approaches, such as cellular, biomechanical, molecular, quantitative, computational and theoretical biology. Areas of particular interest include: Cell and tissue morphogenesis Cell adhesion and migration Cell shape and polarity Biomechanics Theoretical modelling of cell and developmental biology Quantitative biology Stem cell biology Cell differentiation Cell proliferation and cell death Evo-Devo Membrane traffic Metabolic regulation Organ and organoid development Regeneration Mechanisms of Development does not publish descriptive studies of gene expression patterns and molecular screens; for submission of such studies see Gene Expression Patterns.
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Editorial Board Publisher's note Outside Front Cover Regulatory functions of gga-miR-218 in spermatogonial stem cells meiosis by targeting Stra8 Improved early development potence of in vitro fertilization embryos by treatment with tubacin increasing acetylated tubulin of matured porcine oocytes
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