
doi: 10.1007/bf00215056
pmid: 1639442
Methylation patterns in the major histocompatibility complex (MHC) class II Eb locus have been analyzed in cell lines representative of different cell types; in particular those with phenotypes found at various stages of B cell development. A series of variant B cell lymphoma lines which serves as a model in which to investigate mechanisms regulating class II gene expression in normal peripheral B cells has been examined. Eb methylation patterns have also been determined in various healthy mouse tissues. The pattern of methylation of the Eb locus varies between different cell lines and tissue types such that hypomethylation is associated with gene expression. There appears to be a methylation pattern which is permissive for class II gene expression and which is characteristic of a variety of cell lines, but is lost in cell lines representing terminally differentiated class II nonexpressing plasma cells. Another methylation pattern has been identified which is found in cloned cell lines selected for expression of very high levels of cell surface class II product. The patterns of methylation associated with MHC class II expression involve changes in methylation sites located within the first intron and several kilobase pairs 5' of the promoter, but no changes were observed in the 3' end of the locus. Moreover, the different methylation patterns do not map to the prominent CpG rich cluster located 5' of the Eb promoter and which remains completely methylated regardless of transcriptional status.
B-Lymphocytes, Mice, Inbred BALB C, Macrophages, Genes, MHC Class II, Molecular Sequence Data, Restriction Mapping, Fluorescent Antibody Technique, DNA, Flow Cytometry, Methylation, Introns, Cell Line, Interferon-gamma, Mice, Phenotype, Gene Expression Regulation, Antigens, Surface, Animals, Cloning, Molecular
B-Lymphocytes, Mice, Inbred BALB C, Macrophages, Genes, MHC Class II, Molecular Sequence Data, Restriction Mapping, Fluorescent Antibody Technique, DNA, Flow Cytometry, Methylation, Introns, Cell Line, Interferon-gamma, Mice, Phenotype, Gene Expression Regulation, Antigens, Surface, Animals, Cloning, Molecular
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