Suppr超能文献

人类C6基因的结构。

Structure of the human C6 gene.

作者信息

Hobart M J, Fernie B, DiScipio R G

机构信息

MIP Unit, MRC Centre, Cambridge, U.K.

出版信息

Biochemistry. 1993 Jun 22;32(24):6198-205. doi: 10.1021/bi00075a012.

Abstract

The terminal components of the complement system (C6-C9) are related proteins, differing in size and complexity. They seem to be typical mosaic proteins, composed of modules which are homologous with parts of other proteins. Individual elements in a mosaic protein are often bounded by introns in the gene, and where they are duplicated within a polypeptide, partial gene duplication within the gene is responsible. It is often found in such genes that the intron/exon boundaries are of the class 1 type. We have examined the boundaries of 17 of the 18 exons of C6 and five of C7. When considered with published data for C9, only one of the protein elements appears to follow the conventional pattern. These data suggest a more complex evolutionary history for the genes of the terminal complement components than had been anticipated and challenge the notions both that discovery of a recognized protein module is of predictive value in relation to gene structure and that these genes evolved from the simple to the complex.

摘要

补体系统的终末成分(C6 - C9)是相关蛋白,大小和复杂性各异。它们似乎是典型的镶嵌蛋白,由与其他蛋白部分同源的模块组成。镶嵌蛋白中的各个元件通常由基因中的内含子界定,并且当它们在多肽内重复时,基因内的部分基因重复起作用。在这类基因中经常发现内含子/外显子边界属于1类。我们检查了C6的18个外显子中的17个以及C7的5个外显子的边界。结合已发表的C9数据来看,只有一个蛋白质元件似乎遵循传统模式。这些数据表明,补体终末成分的基因进化史比预期的更为复杂,并且对以下两种观念提出了挑战:一是发现一个公认的蛋白质模块对基因结构具有预测价值,二是这些基因是从简单进化到复杂的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验