Suppr超能文献

一种核抑制因子克服了衣藻两个不同核基因突变导致的叶绿体psbD基因产物合成缺陷。

A nuclear suppressor overcomes defects in the synthesis of the chloroplast psbD gene product caused by mutations in two distinct nuclear genes of Chlamydomonas.

作者信息

Wu H Y, Kuchka M R

机构信息

Department of Molecular Biology, Lehigh University, Bethlehem, PA 18015, USA.

出版信息

Curr Genet. 1995 Feb;27(3):263-9. doi: 10.1007/BF00326159.

Abstract

Mutations in two distinct nuclear genes, called NAC 1 and AC-115, of the unicellular green alga Chlamydomonas reinhardtii cause a specific and dramatic reduction in the synthesis of the chloroplast-encoded D2 polypeptide of Photosystem II. The psbD transcript which encodes the D2 protein is present in the mutant strains, but protein pulse-labeling and immunoprecipitation experiments demonstrate that the synthesis of the D2 protein does not occur normally in these cells. These phenotypes are suppressed by an extragenic nuclear suppressor isolated from a pseudorevertant of a nac 1 mutant. This suppressor is neither allele- nor gene-specific in its suppression and is able to overcome the effects of two different mutations in the NAC 1 gene, as well as a mutation in AC-115. The suppressor seems to be specific in its ability to remedy blocks in psbD mRNA translation in the chloroplast. It is not able to restore the translation of another chloroplast-encoded mRNA which is blocked by another nuclear mutation. The suppressor may identify a new nuclear gene specifically involved in the synthesis of the D2 protein in the chloroplast.

摘要

单细胞绿藻莱茵衣藻中两个不同的核基因NAC 1和AC - 115发生突变,会导致光系统II中叶绿体编码的D2多肽的合成出现特定且显著的减少。编码D2蛋白的psbD转录本在突变菌株中存在,但蛋白质脉冲标记和免疫沉淀实验表明,D2蛋白的合成在这些细胞中不能正常发生。这些表型被从nac 1突变体的假回复体中分离出的一个基因外核抑制子所抑制。该抑制子在抑制作用上既不是等位基因特异性的,也不是基因特异性的,并且能够克服NAC 1基因中两种不同突变以及AC - 115中一个突变的影响。该抑制子在补救叶绿体中psbD mRNA翻译受阻方面的能力似乎具有特异性。它无法恢复另一个被另一个核突变阻断的叶绿体编码mRNA的翻译。该抑制子可能鉴定出一个新的核基因,该基因专门参与叶绿体中D2蛋白的合成。

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