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载脂蛋白B基因短片段缺失导致血浆胆固醇水平降低。

Low plasma cholesterol levels caused by a short deletion in the apolipoprotein B gene.

作者信息

Young S G, Northey S T, McCarthy B J

机构信息

Gladstone Foundation Laboratories for Cardiovascular Disease, University of California, San Francisco 94140-0608.

出版信息

Science. 1988 Jul 29;241(4865):591-3. doi: 10.1126/science.3399894.

Abstract

Familial hypobetalipoproteinemia is a syndrome in which the plasma levels of apolipoprotein B (apo-B) and cholesterol are abnormally low. A truncated species of apo-B was identified in the plasma lipoproteins of members of a kindred with familial hypobetalipoproteinemia. DNA sequencing studies on genomic clones and enzymatically amplified genomic DNA samples revealed a four-base pair deletion in the apo-B gene. This short deletion, which results in a frameshift and a premature stop codon, accounts for the truncated apo-B species and explains the low apo-B and low cholesterol levels in this family.

摘要

家族性低β脂蛋白血症是一种血浆载脂蛋白B(apo-B)和胆固醇水平异常低的综合征。在一个患有家族性低β脂蛋白血症的家族成员的血浆脂蛋白中鉴定出一种截短的apo-B。对基因组克隆和酶促扩增的基因组DNA样本进行的DNA测序研究揭示了apo-B基因中的一个四碱基对缺失。这种短缺失导致移码和过早的终止密码子,解释了截短的apo-B种类,并说明了该家族中apo-B和胆固醇水平低的原因。

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