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PMID: 3116083 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mutant human B cell lines deficient in class II major histocompatibility complex transcription.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 139 ·No. 7 ·1987-10-01 ·Pages 2489-95

Calman AF, Peterlin BM

Abstract

By mutagenesis and selection, two independent Ia- mutant cell lines derived from the Ia+ human B cell line Raji were isolated. One mutant failed to express detectable surface HLA-DR and HLA-DQ molecules, while the other expressed very low levels of these molecules. mRNA encoding Ia molecules was correspondingly absent or reduced in these cell lines. In contrast, levels of class I major histocompatibility complex (MHC) mRNA and protein were normal in these cells. The class II MHC genes of the mutant cells were grossly intact, suggesting that the defective expression of these genes was due to an absent or abnormal trans-acting regulatory factor. In vitro nuclear run-on transcription assays and measurement of class II MHC mRNA stability suggested that the specific defect in class II MHC gene expression in both mutant cell lines was at the level of transcription initiation.

MeSH Terms
B-Lymphocytes/immunology,metabolism Gene Expression Regulation/drug effects Histocompatibility Antigens Class II/biosynthesis Humans Interferon-gamma/pharmacology Major Histocompatibility Complex RNA, Messenger/analysis Recombinant Proteins/pharmacology Transcription Factors/deficiency,genetics Transcription, Genetic Tumor Cells, Cultured
Chemicals
Histocompatibility Antigens Class II RNA, Messenger Recombinant Proteins Transcription Factors Interferon-gamma
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Calman A F
Department of Microbiology and Immunology, University of California, San Francisco 94143.
Peterlin B M
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1987-10-01
Pages
2489-95
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIGMS NIH HHS · GM07618 · United States
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