Suppr超能文献

一种可能锚定质体类核的质体包膜DNA结合蛋白的检测与特性分析。

Detection and characterization of a plastid envelope DNA-binding protein which may anchor plastid nucleoids.

作者信息

Sato N, Albrieux C, Joyard J, Douce R, Kuroiwa T

机构信息

Laboratory of Life Science, Tokyo Gakugei University, Japan.

出版信息

EMBO J. 1993 Feb;12(2):555-61. doi: 10.1002/j.1460-2075.1993.tb05687.x.

Abstract

Chloroplast DNA (cpDNA) binds to the envelope membrane of actively dividing chloroplasts (plastids) in young pea leaves. South-western blotting was used to identify and characterize the protein involved in the binding of cpDNA to the envelope membrane. A 130 kDa protein in the inner chloroplast (plastid) envelope membrane binds specific sequences within the cpDNA. These included a 0.41 kbp sequence located upstream of the psaAB gene, a 0.57 kbp sequence located downstream of the petA gene and a 1.2 kbp sequence located within the rpoC2 gene. The protein was detected in the envelope membrane of young pea leaves in which the cpDNA had been located by fluorescence microscopy at the chloroplast periphery, whereas it was undetectable in mature leaves. We therefore propose that the 130 kDa protein is involved in the binding of cpDNA to the envelope membrane, and named it plastid envelope DNA-binding protein.

摘要

叶绿体DNA(cpDNA)与幼嫩豌豆叶片中活跃分裂的叶绿体(质体)的包膜膜结合。采用Southwestern印迹法来鉴定和表征参与cpDNA与包膜膜结合的蛋白质。叶绿体(质体)内膜中的一种130 kDa蛋白质与cpDNA内的特定序列结合。这些序列包括位于psaAB基因上游的0.41 kbp序列、位于petA基因下游的0.57 kbp序列以及位于rpoC2基因内的1.2 kbp序列。该蛋白质在幼嫩豌豆叶片的包膜膜中被检测到,通过荧光显微镜观察发现cpDNA位于叶绿体周边,而在成熟叶片中则检测不到。因此,我们认为130 kDa蛋白质参与了cpDNA与包膜膜的结合,并将其命名为质体包膜DNA结合蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76b6/413238/1a287fdacd7a/emboj00074-0186-a.jpg

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