Literature DB >> 8497268

The octamer/mu E4 region of the immunoglobulin heavy-chain enhancer mediates gene repression in myeloma x T-lymphoma hybrids.

L Shen1, S Lieberman, L A Eckhardt.   

Abstract

We have shown previously that the immunoglobulin heavy-chain enhancer acts as a repressor of gene transcription in hybrids between immunoglobulin-producing myelomas and a T-lymphoma line. We have now mapped this repressive activity to a 51-bp enhancer subfragment which contains the octamer and mu E4 protein-binding motifs. Even a single copy of this subfragment will repress gene expression in hybrid cells. Mutational analyses of the repressor fragment suggest that in non-B cells, a strong transcriptional repressor(s) functions through the same motifs important for gene activation in B cells. Changes in chromatin structure that accompany reporter gene repression suggest a general mechanism for prohibiting immunoglobulin heavy-chain locus activation in inappropriate cell types.

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Year:  1993        PMID: 8497268      PMCID: PMC359823          DOI: 10.1128/mcb.13.6.3530-3540.1993

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


  47 in total

1.  Extinction of expression of immunoglobulin genes in myeloma X fibroblast somatic cell hybrids.

Authors:  A Greenberg; R Ber; Z Kra-Oz; R Laskov
Journal:  Mol Cell Biol       Date:  1987-02       Impact factor: 4.272

2.  Electroporation for the efficient transfection of mammalian cells with DNA.

Authors:  G Chu; H Hayakawa; P Berg
Journal:  Nucleic Acids Res       Date:  1987-02-11       Impact factor: 16.971

3.  Identification of murine nuclear proteins that bind to the conserved octamer sequence of the immunoglobulin promoter region.

Authors:  J H Hanke; N F Landolfi; P W Tucker; J D Capra
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

4.  Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter.

Authors:  D A Melton; P A Krieg; M R Rebagliati; T Maniatis; K Zinn; M R Green
Journal:  Nucleic Acids Res       Date:  1984-09-25       Impact factor: 16.971

5.  B lineage--specific interactions of an immunoglobulin enhancer with cellular factors in vivo.

Authors:  A Ephrussi; G M Church; S Tonegawa; W Gilbert
Journal:  Science       Date:  1985-01-11       Impact factor: 47.728

6.  Cell-type specific protein binding to the enhancer of simian virus 40 in nuclear extracts.

Authors:  I Davidson; C Fromental; P Augereau; A Wildeman; M Zenke; P Chambon
Journal:  Nature       Date:  1986 Oct 9-15       Impact factor: 49.962

7.  A genetic analysis of extinction: trans-dominant loci regulate expression of liver-specific traits in hepatoma hybrid cells.

Authors:  A M Killary; R E Fournier
Journal:  Cell       Date:  1984-09       Impact factor: 41.582

8.  Identification and characterization of two functional domains within the murine heavy-chain enhancer.

Authors:  M Kiledjian; L K Su; T Kadesch
Journal:  Mol Cell Biol       Date:  1988-01       Impact factor: 4.272

9.  Cell-type-specific contacts to immunoglobulin enhancers in nuclei.

Authors:  G M Church; A Ephrussi; W Gilbert; S Tonegawa
Journal:  Nature       Date:  1985 Feb 28-Mar 6       Impact factor: 49.962

10.  Cell type-specificity elements of the immunoglobulin heavy chain gene enhancer.

Authors:  T Gerster; P Matthias; M Thali; J Jiricny; W Schaffner
Journal:  EMBO J       Date:  1987-05       Impact factor: 11.598

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  11 in total

1.  Oct1 is a switchable, bipotential stabilizer of repressed and inducible transcriptional states.

Authors:  Arvind Shakya; Jinsuk Kang; Jeffrey Chumley; Matthew A Williams; Dean Tantin
Journal:  J Biol Chem       Date:  2010-11-04       Impact factor: 5.157

2.  The chicken immunoglobulin lambda light chain gene is transcriptionally controlled by a modularly organized enhancer and an octamer-dependent silencer.

Authors:  S Bulfone-Paus; L Reiners-Schramm; R Lauster
Journal:  Nucleic Acids Res       Date:  1995-06-11       Impact factor: 16.971

3.  ETS-mediated cooperation between basic helix-loop-helix motifs of the immunoglobulin mu heavy-chain gene enhancer.

Authors:  W Dang; X H Sun; R Sen
Journal:  Mol Cell Biol       Date:  1998-03       Impact factor: 4.272

4.  A soluble transcription factor, Oct-1, is also found in the insoluble nuclear matrix and possesses silencing activity in its alanine-rich domain.

Authors:  M K Kim; L A Lesoon-Wood; B D Weintraub; J H Chung
Journal:  Mol Cell Biol       Date:  1996-08       Impact factor: 4.272

5.  Precise alignment of sites required for mu enhancer activation in B cells.

Authors:  B S Nikolajczyk; B Nelsen; R Sen
Journal:  Mol Cell Biol       Date:  1996-08       Impact factor: 4.272

6.  E47 activates the Ig-heavy chain and TdT loci in non-B cells.

Authors:  J K Choi; C P Shen; H S Radomska; L A Eckhardt; T Kadesch
Journal:  EMBO J       Date:  1996-09-16       Impact factor: 11.598

Review 7.  Negative regulation of transcription in eukaryotes.

Authors:  A R Clark; K Docherty
Journal:  Biochem J       Date:  1993-12-15       Impact factor: 3.857

8.  Kappa immunoglobulin promoters and enhancers display developmentally controlled interactions.

Authors:  R Fulton; B Van Ness
Journal:  Nucleic Acids Res       Date:  1993-10-25       Impact factor: 16.971

9.  Displacement of an E-box-binding repressor by basic helix-loop-helix proteins: implications for B-cell specificity of the immunoglobulin heavy-chain enhancer.

Authors:  T Genetta; D Ruezinsky; T Kadesch
Journal:  Mol Cell Biol       Date:  1994-09       Impact factor: 4.272

10.  Cux/CDP homeoprotein is a component of NF-muNR and represses the immunoglobulin heavy chain intronic enhancer by antagonizing the bright transcription activator.

Authors:  Z Wang; A Goldstein; R T Zong; D Lin; E J Neufeld; R H Scheuermann; P W Tucker
Journal:  Mol Cell Biol       Date:  1999-01       Impact factor: 4.272

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