Chan L
Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Biochimie. 1995;77(1-2):75-8. doi: 10.1016/0300-9084(96)88107-7.
Apolipoprotein (apo) B mRNA editing consists of a C-->U conversion of the first base of the codon CAA encoding glutamine 2153 in apoB mRNA to UAA, a stop codon. The cDNA for an apoB mRNA editing protein was recently cloned in rat and human. The human protein contains 236 amino acid residues and exists as a homodimer. The editing protein edits apoB mRNA in vitro only in the presence of tissue complementation factors. There is a leucine-rich motif spanning residues 173-210 of the protein which may be involved in homodimer formation and/or interaction with complementation factors. The requirements for these factors support the existence of an editosome involved in apoB mRNA editing.
载脂蛋白(apo)B信使核糖核酸(mRNA)编辑是指将apoB mRNA中编码谷氨酰胺2153的密码子CAA的第一个碱基由C转换为UAA(一个终止密码子)。最近在大鼠和人类中克隆出了apoB mRNA编辑蛋白的互补脱氧核糖核酸(cDNA)。该人类蛋白含有236个氨基酸残基,并以同源二聚体形式存在。该编辑蛋白仅在组织互补因子存在的情况下在体外编辑apoB mRNA。该蛋白的173 - 210位残基存在一个富含亮氨酸的基序,其可能参与同源二聚体的形成和/或与互补因子的相互作用。对这些因子的需求支持了参与apoB mRNA编辑的编辑体的存在。