Suppr超能文献

内含子的进化:对人类肌营养不良蛋白基因中一个长的、易发生缺失的内含子的分析。

The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene.

作者信息

McNaughton J C, Hughes G, Jones W A, Stockwell P A, Klamut H J, Petersen G B

机构信息

Department of Biochemistry, University of Otago, Dunedin, New Zealand.

出版信息

Genomics. 1997 Mar 1;40(2):294-304. doi: 10.1006/geno.1996.4543.

Abstract

The sequence of a 112-kb region of the human dystrophin (DMD/BMD) gene encompassing the deletion prone intron 7 (110 kb) and the much shorter intron 8 (1.1 kb) has been determined. Recognizable insertion sequences account for approximately 40% of intron 7. LINE-1 and THE-1/LTR sequences occur in intron 7 with significantly higher frequency than would be expected statistically while Alu sequences are underrepresented. Intron 7 also contains numerous mammalian-wide interspersed repeats, a diverse range of medium reiteration repeats of unknown origin, and a sequence derived from a mariner transposon. By contrast, the shorter intron 8 contains no detectable insertion sequences. Dating of the LI and Alu sequences suggests that intron 7 has approximately doubled in size within the past 130 million years, and comparison with the corresponding intron from the pufferfish (Fugu rubripes) suggests that the intron has expanded some 44-fold over a period of 400 million years. The possible contribution of the insertion elements to the instability of intron 7 is discussed.

摘要

已确定人类肌营养不良蛋白(DMD/BMD)基因112kb区域的序列,该区域包含易于发生缺失的内含子7(110kb)和短得多的内含子8(1.1kb)。可识别的插入序列约占内含子7的40%。LINE-1和THE-1/LTR序列在内含子7中的出现频率显著高于统计学预期,而Alu序列的含量不足。内含子7还包含许多全哺乳动物散布重复序列、多种来源不明的中等重复序列以及源自水手转座子的序列。相比之下,较短的内含子8未检测到插入序列。对LINE-1和Alu序列的年代测定表明,内含子7在过去1.3亿年中大小大约增加了一倍,与河豚(红鳍东方鲀)的相应内含子比较表明,该内含子在4亿年的时间里扩大了约44倍。文中讨论了插入元件对内含子7不稳定性的可能贡献。

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