molecular evolution and functional divergence of the cytochrome p450 3 (cyp3) family in actinopterygii (ray-finned fish)分子进化和功能分化的细胞色素p450 3(cyp3)家庭辐鳍鱼纲(鳍刺类鱼).pdfVIP

molecular evolution and functional divergence of the cytochrome p450 3 (cyp3) family in actinopterygii (ray-finned fish)分子进化和功能分化的细胞色素p450 3(cyp3)家庭辐鳍鱼纲(鳍刺类鱼).pdf

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molecular evolution and functional divergence of the cytochrome p450 3 (cyp3) family in actinopterygii (ray-finned fish)分子进化和功能分化的细胞色素p450 3(cyp3)家庭辐鳍鱼纲(鳍刺类鱼)

Molecular Evolution and Functional Divergence of the Cytochrome P450 3 (CYP3) Family in Actinopterygii (Ray- Finned Fish) Jun Yan1,2, Zhonghua Cai1,2* 1 Departments of Biological Science and Biotechnology, Tsinghua University, Beijing, People’s Republic of China, 2 Graduate School at Shenzhen, Tsinghua University, Shenzhen, People’s Republic of China Abstract Background: The cytochrome P450 (CYP) superfamily is a multifunctional hemethiolate enzyme that is widely distributed from Bacteria to Eukarya. The CYP3 family contains mainly the four subfamilies CYP3A, CYP3B, CYP3C and CYP3D in vertebrates; however, only the Actinopterygii (ray-finned fish) have all four subfamilies and detailed understanding of the evolutionary relationship of Actinopterygii CYP3 family members would be valuable. Methods and Findings: Phylogenetic relationships were constructed to trace the evolutionary history of the Actinopterygii CYP3 family genes. Selection analysis, relative rate tests and functional divergence analysis were combined to interpret the relationship of the site-specific evolution and functional divergence in the Actinopterygii CYP3 family. The results showed that the four CYP3 subfamilies in Actinopterygii might be formed by gene duplication. The first gene duplication event was responsible for divergence of the CYP3B/C clusters from ancient CYP3 before the origin of the Actinopterygii, which corresponded to the fish-specific whole genome duplication (WGD). Tandem repeat duplication in each of the homologue clusters produced stable CYP3B, CYP3C, CYP3A and CYP3D subfamilies. Acceleration of asymmetric evolutionary rates and purifying selection together were the main force for the production of new subfamilies and functional divergence in the new subset after gene duplication, whereas positive selection was detected only in th

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