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恒河猴载脂蛋白(a)。序列、进化及合成位点。

Rhesus monkey apolipoprotein(a). Sequence, evolution, and sites of synthesis.

作者信息

Tomlinson J E, McLean J W, Lawn R M

机构信息

Department of Cardiovascular Research, Genentech, Inc., South San Francisco, California 94080.

出版信息

J Biol Chem. 1989 Apr 5;264(10):5957-65.

PMID:2925643
Abstract

Human lipoprotein(a) is a low density lipoprotein-like lipoprotein whose concentration in plasma is correlated with atherosclerosis. The characteristic protein component of lipoprotein(a) is apolipoprotein(a) (apo(a)) which is disulfide-linked to apolipoprotein B-100. Sequencing of rhesus monkey apo(a) cDNA suggests that this protein, like human apo(a), is highly similar to plasminogen. Sequence data suggests that a plasminogen-like protease activity and kringle 1-, 2-, 3-, and 5-like domains are unnecessary for apo(a) function, but a highly repeated kringle four-like domain is important. Liver is the major site of apo(a) RNA synthesis; reduced amounts of message were also found in testes and brain. Co-expression with apoB-100 and plasminogen in rhesus tissues is not mandatory.

摘要

人脂蛋白(a)是一种低密度脂蛋白样脂蛋白,其血浆浓度与动脉粥样硬化相关。脂蛋白(a)的特征性蛋白质成分是载脂蛋白(a)(apo(a)),它通过二硫键与载脂蛋白B-100相连。恒河猴apo(a) cDNA测序表明,这种蛋白质与人apo(a)一样,与纤溶酶原高度相似。序列数据表明,apo(a)功能不需要纤溶酶原样蛋白酶活性以及kringle 1、2、3和5样结构域,但高度重复的kringle 4样结构域很重要。肝脏是apo(a) RNA合成的主要部位;在睾丸和大脑中也发现了少量的信使RNA。在恒河猴组织中,apo(a)与apoB-100和纤溶酶原的共表达并非必需。

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