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解析 M-超家族 conotoxin 的进化和功能。

Characterizing the evolution and functions of the M-superfamily conotoxins.

机构信息

State Key Laboratory of Biocontrol, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, National Engineering Research Center of South China Sea Marine Biotechnology, Department of Biochemistry, College of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China.

出版信息

Toxicon. 2013 Dec 15;76:150-9. doi: 10.1016/j.toxicon.2013.09.020. Epub 2013 Sep 27.

Abstract

Conotoxins from cone snails are valuable in physiology research and therapeutic applications. Evolutionary mechanisms of conotoxins have been investigated in several superfamilies, but there is no phylogenetic analysis on M-superfamily conotoxins. In this study, we characterized identical sequences, gene structure, novel cysteine frameworks, functions and evolutionary mechanisms of M-superfamily conotoxins. Identical M-superfamily conotoxins can be found in different Conus species from the analysis of novel 467 M-superfamily conotoxin sequences and other published M-superfamily conotoxins sequences. M-superfamily conotoxin genes consist of two introns and three exons from the results of genome walking. Eighteen cysteine frameworks were identified from the M-superfamily conotoxins, and 10 of the 18 may be generated from framework III. An analysis between diet types and phylogeny of the M-superfamily conotoxins indicate that M-superfamily conotoxins might not evolve in a concerted manner but were subject to birth-and-death evolution. Codon usage analysis shows that position-specific codon conservation is not restricted to cysteines, but also to other conserved residues. By analysing primary structures and physiological functions of M-superfamily conotoxins, we proposed a hypothesis that insertions and deletions, especially insertions in the third cysteine loop, are involved in the creation of new functions and structures of the M-superfamily conotoxins.

摘要

芋螺毒素是一类具有重要生理活性的小肽,来自海洋腹足纲芋螺,已发现的超过 1200 种,具有多样的结构和功能,是研究离子通道和神经递质的重要工具,在药物开发上具有巨大的应用潜力。

从芋螺毒素的进化机制已经在几个超家族进行了研究,但尚未对 M 超家族芋螺毒素进行系统发育分析。本研究对 M 超家族芋螺毒素的特征、基因结构、新的半胱氨酸框架、功能和进化机制进行了研究。通过对新的 467 种 M 超家族芋螺毒素序列和其他已发表的 M 超家族芋螺毒素序列的分析,发现了不同 Conus 物种中的相同 M 超家族芋螺毒素。从基因组步移的结果可知,M 超家族芋螺毒素基因由两个内含子和三个外显子组成。从 M 超家族芋螺毒素中鉴定出 18 个半胱氨酸框架,其中 10 个可能来自框架 III。M 超家族芋螺毒素的饮食类型与系统发育分析表明,M 超家族芋螺毒素可能不是协同进化的,而是受到“诞生-死亡”进化的影响。密码子使用分析表明,位置特异性密码子保守性不仅限于半胱氨酸,还包括其他保守残基。通过分析 M 超家族芋螺毒素的一级结构和生理功能,我们提出了一个假设,即插入和缺失,特别是在第三半胱氨酸环中的插入,可能参与了 M 超家族芋螺毒素新功能和结构的产生。

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