Suppr超能文献

利用构巢曲霉的一个异源基因拯救线粒体ATP合酶亚基8缺陷的酵母。

Rescue of yeast defective in mitochondrial ATP synthase subunit 8 by a heterologous gene from Aspergillus nidulans.

作者信息

Straffon A F, Nagley P, Devenish R J

机构信息

Department of Biochemistry, Monash University, Clayton, Victoria, Australia.

出版信息

Biochem Biophys Res Commun. 1994 Sep 30;203(3):1567-73. doi: 10.1006/bbrc.1994.2365.

Abstract

Mitochondrial ATP synthase subunit 8 of the yeast Saccharomyces cerevisiae and of the filamentous fungus Aspergillus nidulans have the same length and similar structural motifs. However, the two proteins share only 50% identical residues, with the conserved residues being concentrated in the N- and C-terminal domains. We have investigated whether it is amino acid sequence or overall structural motifs that are required for subunit 8 function. PCR was used to construct a gene encoding A. nidulans subunit 8 fused to an N-terminal cleavable mitochondrial targeting sequence. Following expression in the nucleus of a yeast strain deficient in subunit 8, the chimaeric precursor targeted the subunit 8 protein back to the mitochondrion. The A. nidulans subunit 8 was found to be able to restore growth on non-fermentable substrate at 18 degrees C and 28 degrees C, but not at 36 degrees C. Given the sequence divergence between subunit 8 of A. nidulans and that of S. cerevisiae, this finding suggests that common structural motifs are important for subunit 8 function.

摘要

酿酒酵母和构巢曲霉的线粒体ATP合酶亚基8具有相同的长度和相似的结构基序。然而,这两种蛋白质只有50%的相同残基,保守残基集中在N端和C端结构域。我们研究了亚基8功能所需的是氨基酸序列还是整体结构基序。使用PCR构建了一个编码与N端可切割线粒体靶向序列融合的构巢曲霉亚基8的基因。在缺乏亚基8的酵母菌株的细胞核中表达后,嵌合前体将亚基8蛋白靶向回到线粒体。发现构巢曲霉亚基8能够在18℃和28℃下恢复在非发酵底物上的生长,但在36℃下不能。鉴于构巢曲霉和酿酒酵母亚基8之间的序列差异,这一发现表明共同的结构基序对亚基8的功能很重要。

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