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Comparative Study
. 1990 Jun;87(12):4590-4.
doi: 10.1073/pnas.87.12.4590.

Regulation of the class II-associated invariant chain gene in normal and mutant B lymphocytes

Affiliations
Comparative Study

Regulation of the class II-associated invariant chain gene in normal and mutant B lymphocytes

C Doyle et al. Proc Natl Acad Sci U S A. 1990 Jun.

Abstract

The invariant chain protein is intracellularly associated with class II major histocompatibility proteins. In many cases, the expression of these molecules appears to be regulated in a similar manner. Contained within the promoter of the invariant chain gene are sequences (X and I gamma 1) that are similar to the X and Y box elements of class II genes, suggesting that these sequences might be involved in its regulation. DNase I footprinting reveals additional cis-acting elements (I gamma 2 and I gamma 3) that contain sequence similarities to NF-kappa B and/or H2TF1/KBF1 recognition sequences. A series of fusion constructs with the chloramphenicol acetyltransferase reporter gene were used to analyze the role of these sequences (I gamma 1, I gamma 2, I gamma 3, and X and Y elements) in both normal and mutant B lymphocytes. These data suggest the likelihood of multiple X box proteins in B cells, which can act as both negative and positive regulatory factors.

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References

    1. Mol Immunol. 1979 Jan;16(1):51-60 - PubMed
    1. Annu Rev Immunol. 1990;8:681-715 - PubMed
    1. Mol Cell Biol. 1982 Sep;2(9):1044-51 - PubMed
    1. Nucleic Acids Res. 1983 Mar 11;11(5):1475-89 - PubMed
    1. J Exp Med. 1983 Mar 1;157(3):1053-8 - PubMed

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