TLR4型
空等位基因
错义突变
生物
基因
外显子
突变
信号转导
免疫系统
等位基因
受体
脂多糖
分子生物学
遗传学
免疫学
作者
Alexander Poltorak,Xiaolong He,Irina Smirnova,Mu-Ya Liu,Christophe Van Huffel,Xin Du,Dale Birdwell,Erica Alejos,Maria João Silva,Chris Galanos,Marina A. Freudenberg,Paola Ricciardi‐Castagnoli,Betsy Layton,Bruce Beutler
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1998-12-11
卷期号:282 (5396): 2085-2088
被引量:7605
标识
DOI:10.1126/science.282.5396.2085
摘要
Mutations of the gene Lps selectively impede lipopolysaccharide (LPS) signal transduction in C3H/HeJ and C57BL/10ScCr mice, rendering them resistant to endotoxin yet highly susceptible to Gram-negative infection. The codominant Lpsd allele of C3H/HeJ mice was shown to correspond to a missense mutation in the third exon of the Toll-like receptor-4 gene (Tlr4), predicted to replace proline with histidine at position 712 of the polypeptide chain. C57BL/10ScCr mice are homozygous for a null mutation of Tlr4. Thus, the mammalian Tlr4 protein has been adapted primarily to subserve the recognition of LPS and presumably transduces the LPS signal across the plasma membrane. Destructive mutations of Tlr4 predispose to the development of Gram-negative sepsis, leaving most aspects of immune function intact.
科研通智能强力驱动
Strongly Powered by AbleSci AI