Pereira João Pedro, Girard Robert, Chaby Richard, Cumano Ana, Vieira Paulo
Unité du Développement des Lymphocytes, CNRS URA 1961, Institut Pasteur, 25 Rue du Docteur Roux, 75015 Paris, France.
Nat Immunol. 2003 May;4(5):464-70. doi: 10.1038/ni917. Epub 2003 Mar 31.
Defects in the gene encoding Toll-like receptor 4 (Tlr4) result in impaired responses to lipopolysaccharide (LPS), rendering mice sensitive to infections by Gram-negative bacteria. C3H/HeJ mice have a codominant allele with a mutation in Tlr4, which results in an intermediate response to LPS in F1 mice from crosses of responder and C3H/HeJ mice. Here we show that this intermediate response to LPS is due to monoallelic expression of Tlr4. Allele usage is maintained during clonal expansion, a situation that resembles allelic exclusion. In contrast, Tlr4 is deleted on the recessive C57BL/10ScCr allele and all cells from F1 mice from crosses of responder and C57BL/10ScCr mice express TLR4 protein. Thus, Tlr4 is an autosomal gene whose expression is regulated similarly to that of genes on the X chromosome.
编码Toll样受体4(Tlr4)的基因缺陷会导致对脂多糖(LPS)的反应受损,使小鼠对革兰氏阴性菌感染敏感。C3H/HeJ小鼠有一个共显性等位基因,其Tlr4发生突变,这导致来自反应者与C3H/HeJ小鼠杂交的F1小鼠对LPS产生中间反应。我们在此表明,这种对LPS的中间反应是由于Tlr4的单等位基因表达。等位基因的使用在克隆扩增过程中得以维持,这种情况类似于等位基因排斥。相比之下,隐性C57BL/10ScCr等位基因上的Tlr4被删除,来自反应者与C57BL/10ScCr小鼠杂交的F1小鼠的所有细胞都表达TLR4蛋白。因此,Tlr4是一个常染色体基因,其表达的调控方式与X染色体上的基因类似。