Literature DB >> 1922039

Novel protein-DNA interactions associated with increased immunoglobulin transcription in response to antigen plus interleukin-5.

C F Webb1, C Das, S Eaton, K Calame, P W Tucker.   

Abstract

Although much has been learned about basal levels of immunoglobulin (Ig) transcription, the regulatory effects of cytokines and antigen (Ag) upon Ig expression in lymphocytes have not been fully characterized. We previously reported that Ag plus interleukin-5 (IL-5) caused increased steady-state Ig mRNA levels in Ag-specific cell lines. In this study, we have identified a region between -250 and -125 bp 5' of the Ig transcription start site that is necessary for the induction of increased mu mRNA levels by Ag plus IL-5. Mobility shift and UV cross-linking studies indicated that IL-5 plus Ag induced increased protein binding to this region. Furthermore, this sequence was found to be closely related to another A + T-rich sequence at -525 bp 5' of the transcription start site. Both sequences exhibited similar B-cell-specific and inducible protein binding. Our data suggest that treatment with IL-5 plus Ag induces several DNA-binding proteins, some of which may participate in increasing Ig transcription above basal levels by binding to sequences 5' of the octamer motif.

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Year:  1991        PMID: 1922039      PMCID: PMC361554          DOI: 10.1128/mcb.11.10.5197-5205.1991

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  42 in total

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  23 in total

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7.  Loss of Bright/ARID3a function promotes developmental plasticity.

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9.  Bruton's tyrosine kinase regulates immunoglobulin promoter activation in association with the transcription factor Bright.

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10.  Transgenic mice expressing dominant-negative bright exhibit defects in B1 B cells.

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