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PMID: 1401921 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Regulation of transcription of the germ-line Ig alpha constant region gene by an ATF element and by novel transforming growth factor-beta 1-responsive elements.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 149 ·No. 9 ·1992-11-01 ·Pages 2914-25

Lin YC, Stavnezer J

Abstract

Inasmuch as transcription of unrearranged, or germ-line, Ig CH genes appears to direct switch recombination, understanding the regulation of this transcription is essential for understanding the regulation of class switching. Transforming growth factor-beta 1 (TGF-beta 1) induces germ-line alpha transcripts and increases class switching to IgA in the I.29 mu B lymphoma and in Peyer's patch and splenic B cells. It has been previously demonstrated that induction of germ-line alpha transcripts by TGF-beta occurs at the transcriptional level in I.29 mu cells. We now demonstrate that the DNA segment located 5' to the initiation sites of germ-line alpha RNA drives expression of a luciferase reporter gene construct in transient transfection experiments. Full constitutive expression requires no more than 106 bp of the 5' flanking segment. By creating a series of deletion and substitution mutations, we have demonstrated that an ATF/CRE site residing within this region is very important for constitutive expression of the germ-line alpha promoter, but mutation of this motif does not diminish TGF-beta induction. Inducibility by TGF-beta requires additional sequences residing between -128 to -106 relative to the first RNA initiation site. Two copies of a tandemly repeated sequence 5' CA-CAG(G)CCAGAC 3' (termed Ig alpha TGF-beta-RE) are located in the region from -127 to -105. An oligonucleotide containing multimers of these repeats confers TGF-beta inducibility to a heterologous promoter. An additional copy of the TGF-beta-RE was identified at -41/-30 and its deletion reduces the TGF-beta response. Thus, we conclude that tandem repeats of a novel TGF-beta-RE are the positive regulatory element for the TGF-beta response. Our study provides further evidence that TGF-beta directs class switching to IgA through induction of transcription of the germ-line C alpha gene and demonstrates that TGF-beta can activate the promoter for the germ-line alpha gene.

MeSH Terms
Activating Transcription Factors Animals Base Sequence Blood Proteins/physiology Cell Line Gene Expression Regulation/physiology Genes, Immunoglobulin/physiology Immunoglobulin A/biosynthesis Immunoglobulin Constant Regions/biosynthesis Immunoglobulin alpha-Chains/biosynthesis Mice Molecular Sequence Data Mutagenesis, Site-Directed Neoplasm Proteins/physiology Oligonucleotide Probes Promoter Regions, Genetic/physiology Restriction Mapping Sequence Homology, Nucleic Acid Transcription Factors/physiology Transcription, Genetic/physiology Transfection Transforming Growth Factor beta/physiology
Chemicals
Activating Transcription Factors Blood Proteins Immunoglobulin A Immunoglobulin Constant Regions Immunoglobulin alpha-Chains Neoplasm Proteins Oligonucleotide Probes Transcription Factors Transforming Growth Factor beta
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lin Y C
Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester 01655.
Stavnezer J
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1992-11-01
Pages
2914-25
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · 1T32-AI07349 · United States
NIAID NIH HHS · AI23283 · United States
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