Smith M A, Stobart A K, Shewry P R, Napier J A
Department of Botany, University of Bristol, UK.
Plant Mol Biol. 1994 Jun;25(3):527-37. doi: 10.1007/BF00043880.
A full-length clone encoding cytochrome b5 has been isolated from a tobacco leaf cDNA library in lambda gt11 by PCR using degenerate primers. This cDNA encodes a protein of 139 residues which exhibits a high degree of homology to other cytochrome b5s, the message for which is expressed predominantly in developing seeds and in pigmented flower tissue. In the developing tobacco seed the mRNA is abundant at very early stages (< 10 days after flowering). Southern analysis indicated that more than one gene encodes cytochrome b5 in the tobacco genome. In vitro transcription and translation studies of the cDNA indicated that the protein inserts into the ER membrane by a non-SRP-mediated pathway and that the C-terminus of the protein is required for targeting and insertion.
利用简并引物通过聚合酶链反应(PCR)从λgt11载体中的烟草叶片cDNA文库中分离出了一个编码细胞色素b5的全长克隆。该cDNA编码一个由139个氨基酸残基组成的蛋白质,它与其他细胞色素b5具有高度同源性,其信使核糖核酸(mRNA)主要在发育中的种子和有色花组织中表达。在发育中的烟草种子里,mRNA在非常早期阶段(开花后<10天)就大量存在。Southern分析表明,烟草基因组中不止一个基因编码细胞色素b5。对该cDNA的体外转录和翻译研究表明,该蛋白质通过非信号识别颗粒(SRP)介导的途径插入内质网(ER)膜,并且该蛋白质的C末端对于靶向和插入是必需的。