Suppr超能文献

马克斯克鲁维酵母在乙醇脱氢酶2(ADH2)下游呈现出酿酒酵母祖先的基因组组织形式。

Kluyveromyces marxianus exhibits an ancestral Saccharomyces cerevisiae genome organization downstream of ADH2.

作者信息

Ladrière J M, Georis I, Guérineau M, Vandenhaute J

机构信息

Unité de Recherche en Biologie Moléculaire, Laboratoire de Génétique Moléculaire, Facultés Universitaires Notre-Dame de la Paix, Namur, Belgium.

出版信息

Gene. 2000 Sep 5;255(1):83-91. doi: 10.1016/s0378-1119(00)00310-3.

Abstract

In Saccharomyces cerevisiae, the alcohol dehydrogenase genes ADH1 and ADH5 are part of a duplicated block of genome, thought to originate from a genome-wide duplication posterior to the divergence from the Kluyveromyces lineage. We report here the characterization of Kluyveromyces marxianus ADH2 and the five genes found in its immediate downstream region, MRPS9, YOL087C, RPB5, RIB7 and SPP381. The order of these six genes reflects the structure of the ancestral S. cerevisiae genome before the duplication that formed the blocks including ADH1 on chromosome XV and ADH5 on chromosome II, indicating these ADH genes share a direct ancestor. On the one hand, the two genes found immediately downstream of KmADH2 are located, for the first, downstream ADH5 and, for the second, downstream ADH1 in S. cerevisiae. On the other hand, the order of the paralogs included in the blocks of ADH1 and ADH5 in S. cerevisiae suggests that two of them have been inverted within one block after its formation, and that inversion is confirmed by the gene order observed in K. marxianus.

摘要

在酿酒酵母中,乙醇脱氢酶基因ADH1和ADH5是基因组重复区域的一部分,该区域被认为起源于与克鲁维酵母谱系分化后的全基因组复制。我们在此报告马克斯克鲁维酵母ADH2及其紧邻下游区域发现的五个基因MRPS9、YOL087C、RPB5、RIB7和SPP381的特征。这六个基因的排列顺序反映了酿酒酵母基因组在形成包含第十五号染色体上的ADH1和第二号染色体上的ADH5的区域的复制之前的祖先结构,表明这些ADH基因有一个直接的共同祖先。一方面,在马克斯克鲁维酵母ADH2紧邻下游发现的两个基因,第一个位于酿酒酵母中ADH5的下游,第二个位于ADH 的下游。另一方面酿酒酵母中ADH1和ADH5区域内旁系同源基因的排列顺序表明,其中两个旁系同源基因在该区域形成后在一个区域内发生了倒置,而这种倒置在马克斯克鲁维酵母中观察到的基因顺序中得到了证实。

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