Lin-Lee Y C, Kao F T, Cheung P, Chan L
Biochemistry. 1985 Jul 2;24(14):3751-6. doi: 10.1021/bi00335a050.
Apolipoprotein E (apoE) binds to specific cell-surface receptors and appears to be an important determinant in lipoprotein metabolism in man. Cloned human apoE cDNA (pAE155) was used as a probe in chromosome mapping studies to detect the structural gene sequences in human--Chinese hamster cell hybrids. Southern blot analysis of HincII-digested DNAs from 13 hybrids localized the gene to human chromosome 19. This observation indicates that apoE is syntenic to at least two other genes related to lipid metabolism, those for the low-density lipoprotein (LDL) receptor (the LDLR) and apoC-II. The cloned apoE cDNA was further used to detect the presence of apoE mRNA in RNA extracts of various human and baboon tissues. Northern gel analysis using the 32P-labeled pAE155 as a probe demonstrated the presence of hybridizable apoE mRNAs in human liver and in baboon liver, intestine, spleen, kidney, adrenal gland, and brain but not in baboon skeletal muscle. The apoE mRNAs appear to be intact and migrate on an agarose gel under denaturing conditions at approximately 18 S. To assay for the biological activity of the apoE mRNAs in these tissues, they were translated in a reticulocyte lysate system in vitro. Immunoprecipitation with an apoE-specific antiserum followed by sodium dodecyl sulfate gel electrophoresis and fluorography demonstrated that immunoreactive apoE with the expected apparent size was a product of translation of mRNAs from baboon liver, intestine, kidney, spleen, and brain but not that from baboon skeletal muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
载脂蛋白E(apoE)与特定的细胞表面受体结合,似乎是人类脂蛋白代谢的一个重要决定因素。克隆的人apoE cDNA(pAE155)在染色体定位研究中用作探针,以检测人-中国仓鼠细胞杂种中的结构基因序列。对13个杂种的HincII消化DNA进行的Southern印迹分析将该基因定位到人类19号染色体上。这一观察结果表明,apoE与至少另外两个与脂质代谢相关的基因同线,即低密度脂蛋白(LDL)受体(LDLR)和apoC-II的基因。克隆的apoE cDNA进一步用于检测各种人类和狒狒组织的RNA提取物中apoE mRNA的存在。使用32P标记的pAE155作为探针进行的Northern凝胶分析表明,在人肝脏以及狒狒肝脏、肠道、脾脏、肾脏、肾上腺和大脑中存在可杂交的apoE mRNA,但在狒狒骨骼肌中不存在。apoE mRNA似乎是完整的,在变性条件下在琼脂糖凝胶上迁移,大小约为18S。为了测定这些组织中apoE mRNA的生物学活性,将它们在体外网织红细胞裂解物系统中进行翻译。用apoE特异性抗血清进行免疫沉淀,然后进行十二烷基硫酸钠凝胶电泳和荧光自显影,结果表明,具有预期表观大小的免疫反应性apoE是狒狒肝脏、肠道、肾脏、脾脏和大脑中mRNA翻译的产物,而不是狒狒骨骼肌中mRNA翻译的产物。(摘要截短于250字)