遗传 ›› 2010, Vol. 32 ›› Issue (1): 87-94.

• 研究报告 • 上一篇    

CVNH 结构域进化分析及选择压力检测

齐小琼,高磊,王艇   

  1. 中国科学院武汉植物园
  • 收稿日期:2009-05-27 修回日期:2009-08-25 出版日期:2010-01-20 发布日期:2010-01-20
  • 通讯作者: 齐小琼 E-mail:tingwang@wbgcas.cn

Phylogenetic analysis and detections of selective pressure on the CVNH domains

  • Received:2009-05-27 Revised:2009-08-25 Online:2010-01-20 Published:2010-01-20

摘要:

蓝藻抗病毒蛋白-N(Cyanovirin-N,CV-N)具有广谱抗病毒活性;其同源物构成 CVNH 蛋白家族,并且家族成员的抗人类免疫缺陷病毒结构域在进化上非常保守。本研究通过重建基因树对 CVNH 结构域的“零散分布”特点作了更为细致的了解,发现在黑曲霉、费氏曲菌、产黄青霉、粗糙脉孢霉、蓝杆藻和水蕨等物种中该结构域存在多份拷贝。在此基础上,分别采用机理式模型和 MEC 模型对 CVNH 结构域序列位点进行适应性进化分析,结果显示:(1)两类模型均未检测到统计上显著的正选择位点;(2)净化选择对 CVNH 起主导作用;(3)MEC 模型更适合所研究数据。进一步使用“支-特异”模型和“支-位点”模型对蓝杆菌菌株7822和7424的祖先分支进行检测,发现该分支经历过适应性进化,并且鉴定出6 个正选择位点(34L、63L、13H、76C、78K 和 80I)。这些结果对后续的 CVNH 功能验证和借助基因工程手段改良蛋白的抗病毒活性具重要意义。

关键词: 蓝藻抗病毒蛋白-N, 基因复制, 净化选择, 适应性进化, CVNH 基因家族

Abstract:

Cyanovirin-N (CV-N) is a novel protein with broad-spectrum antiviral activity. Its homologs constitute a protein family named CVNH (Cyanovirin-N homology), all possessing the evolutionarily conserved anti-HIV (Human immunodeficiency virus) domain. In this research, more details about the patchy organism distribution of CVNH domain have been revealed by reconstructing gene trees. And duplicated CVNH sequences have also been identified in a wide range of species including Aspergillus niger, Neosartorya fischeri NRRL 181, Penicillium chrysogenum Wisconsin 54-1255, Neurospora crassa, Cyanothece sp. PCC and Ceratopteris richardii. Besides these findings, both the mechanistic and mechanistic-empirical combination (MEC) models were used to analyze the adaptive evolution of amino acid sites in the CVNH domain. Our results showed that: (i) neither model reveals significant sites undergoing positive selection; (ii) purifying selection has played a dominant role during CVNH evolution; and (iii) the MEC model better fits the CVNH data set. Furthermore, the ancestral branch leading to Cyanothece sp. PCC 7822 and 7424 were examined by using “branch-specific” and “branch-site” models. Six positively selected sites (34L, 63L, 13H, 76C, 78K and 80I) were identified on the branch. This research provides a basis for future functional test of CVNHs as well as enhancing their antiviral activity through genetic modification.

Key words: CVNH family, cyanovirin-N, gene duplication, purifying selection, adaptive evolution