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PMID: 1639801 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

V(D)J recombination on minichromosomes is not affected by transcription.

The Journal of biological chemistry ·Vol. 267 ·No. 22 ·1992-08-05 ·Pages 15613-9

Hsieh CL, McCloskey RP, Lieber MR

Abstract

It has been shown previously by others that transcription is temporally correlated with the onset of V(D)J recombination at the endogenous antigen receptor loci. We have been interested in determining whether this temporal correlation indicates a causal connection between these two processes. We have compared V(D)J recombination minichromosome substrates that have transcripts running through the recombination zone with substrates that do not in a transient transfection assay. In this system, the substrates acquire a minichromosome conformation within the first several hours after transfection. We find that the substrates recombine equally well over a 100-fold range in transcriptional variation. In additional studies, we have taken substrates that have low levels of transcription and inhibited transcription further by methylating the substrate DNA or by treating the cells with a general transcription inhibitor (alpha-amanitin). Although these treatments decrease the level of expression an additional 10-100-fold, there is still no observable effect on V(D)J recombination. Based on these results, we conclude that transcription is not necessary for the V(D)J reaction mechanism and does not alter substrate structure at the DNA level or at the simplest levels of chromatin structure in a way that affects the reaction.

MeSH Terms
Abelson murine leukemia virus/genetics Animals B-Lymphocytes/immunology Cell Line, Transformed Chromosomes/physiology DNA Replication Gene Rearrangement Genes, Immunoglobulin Kinetics Luciferases/genetics,metabolism Mice Models, Genetic Plasmids Receptors, Antigen, T-Cell/genetics Recombinant Proteins/metabolism Recombination, Genetic Restriction Mapping T-Lymphocytes/immunology Transcription, Genetic Transfection
Chemicals
Receptors, Antigen, T-Cell Recombinant Proteins Luciferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hsieh C L
Department of Pathology, Stanford University School of Medicine, California 94305-5324.
McCloskey R P
Lieber M R
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-08-05
Pages
15613-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIAID NIH HHS · 5T32 AI 07290-07 · United States
NIGMS NIH HHS · GM43236 · United States
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