Literature DB >> 12665857

Monoallelic expression of the murine gene encoding Toll-like receptor 4.

João Pedro Pereira1, Robert Girard, Richard Chaby, Ana Cumano, Paulo Vieira.   

Abstract

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.

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Year:  2003        PMID: 12665857     DOI: 10.1038/ni917

Source DB:  PubMed          Journal:  Nat Immunol        ISSN: 1529-2908            Impact factor:   25.606


  23 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-14       Impact factor: 11.205

5.  Monoallelic expression of Krt12 gene during corneal-type epithelium differentiation of limbal stem cells.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2010-04-14       Impact factor: 4.799

6.  Differentially methylated alleles in a distinct region of the human interleukin-1alpha promoter are associated with allele-specific expression of IL-1alpha in CD4+ T cells.

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Journal:  Blood       Date:  2006-06-20       Impact factor: 22.113

7.  Monoallelic expression of mouse Cd4 gene.

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Journal:  Mamm Genome       Date:  2004-08       Impact factor: 2.957

8.  FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.

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Journal:  J Clin Invest       Date:  2004-07       Impact factor: 14.808

9.  Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies.

Authors:  Juan Li; Anthony J Bench; George S Vassiliou; Nasios Fourouclas; Anne C Ferguson-Smith; Anthony R Green
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10.  RNA sequencing-based screen for reactivation of silenced alleles of autosomal genes.

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Journal:  G3 (Bethesda)       Date:  2022-02-04       Impact factor: 3.542

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