Suppr超能文献

胆固醇结石形成的遗传分析:寻找Lith(胆结石)基因。

Genetic analysis of cholesterol gallstone formation: searching for Lith (gallstone) genes.

作者信息

Wang David Q-H, Afdhal Nezam H

机构信息

Liver Center, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, DA 601, Boston, MA 02215, USA.

出版信息

Curr Gastroenterol Rep. 2004 Apr;6(2):140-50. doi: 10.1007/s11894-004-0042-1.

Abstract

The genetics of cholesterol cholelithiasis is complex because a number of interacting genes regulate biliary cholesterol homeostasis. Quantitative trait locus (QTL) analysis is a powerful method for identifying primary rate-limiting genetic defects and discriminating them from secondary downstream lithogenic effects caused by mutations of the primary genes. The subsequent positional cloning of such genes responsible for QTLs may lead to the discovery of pathophysiologic functions of Lith (gallstone) genes. In this review, we present a map of candidate genes for Lith genes that may determine gallstone susceptibility in mice. The physical-chemical, pathophysiologic, and genetic studies of Lith genes in bile, liver, gallbladder, and intestine will be crucial for elucidating the genetic mechanisms of cholesterol gallstone disease in mice and in humans. Because exceptionally close homology exists between mouse and human genomes, the orthologous human LITH genes can often be recognized after mouse genes are identified.

摘要

胆固醇性胆结石的遗传学很复杂,因为许多相互作用的基因调节胆汁胆固醇的稳态。数量性状基因座(QTL)分析是一种强大的方法,用于识别主要的限速遗传缺陷,并将它们与由主要基因突变引起的继发性下游致石效应区分开来。随后对负责QTL的此类基因进行定位克隆可能会导致发现Lith(胆结石)基因的病理生理功能。在本综述中,我们展示了一张可能决定小鼠胆结石易感性的Lith基因候选基因图谱。对胆汁、肝脏、胆囊和肠道中Lith基因的物理化学、病理生理和遗传学研究对于阐明小鼠和人类胆固醇胆结石疾病的遗传机制至关重要。由于小鼠和人类基因组之间存在异常紧密的同源性,在鉴定出小鼠基因后,通常可以识别出直系同源的人类LITH基因。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验