Literature DB >> 2547524

Role of the octamer motif in hybrid cell extinction of immunoglobulin gene expression: extinction is dominant in a two enhancer system.

H Yu1, B Porton, L Y Shen, L A Eckhardt.   

Abstract

We have shown previously that genes activated by the immunoglobulin heavy chain (IgH) enhancer or promoter in mouse myeloma cells are extinguished upon fusion of the myeloma with a mouse T cell lymphoma. Here we show that the conserved octamer sequence shared by the IgH enhancer and promoter, when multimerized to form a tissue-specific enhancer, can also render a gene extinguishable under the same experimental conditions. Extinction, however, is not correlated with either absence of the tissue-specific transcription factor OTF-2 or loss of its ability to bind the octamer sequence. It was also found that extinction mediated by the IgH enhancer is dominant to transcriptional activation by the SV40 enhancer. We propose, therefore, that the T cell-negative regulator responsible for IgH gene extinction does not simply prevent IgH enhancer activation but interferes with gene expression more directly, perhaps by disrupting the transcription complex established as a result of tissue-specific enhancer activation.

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Year:  1989        PMID: 2547524     DOI: 10.1016/0092-8674(89)90425-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  33 in total

1.  Variegated expression of the endogenous immunoglobulin heavy-chain gene in the absence of the intronic locus control region.

Authors:  D Ronai; M Berru; M J Shulman
Journal:  Mol Cell Biol       Date:  1999-10       Impact factor: 4.272

2.  Oct2 transactivation from a remote enhancer position requires a B-cell-restricted activity.

Authors:  A Annweiler; M Müller-Immerglück; T Wirth
Journal:  Mol Cell Biol       Date:  1992-07       Impact factor: 4.272

3.  Interaction of basal positive and negative transcription elements controls repression of the proximal rat prolactin promoter in nonpituitary cells.

Authors:  S M Jackson; C A Keech; D J Williamson; A Gutierrez-Hartmann
Journal:  Mol Cell Biol       Date:  1992-06       Impact factor: 4.272

4.  Identification of USF as the ubiquitous murine factor that binds to and stimulates transcription from the immunoglobulin lambda 2-chain promoter.

Authors:  L A Chang; T Smith; P Pognonec; R G Roeder; H Murialdo
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

5.  Silencing of the expression of the immunoglobulin kappa gene in non-B cells.

Authors:  J W Pierce; A M Gifford; D Baltimore
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

6.  Common factor 1 is a transcriptional activator which binds in the c-myc promoter, the skeletal alpha-actin promoter, and the immunoglobulin heavy-chain enhancer.

Authors:  K J Riggs; K T Merrell; G Wilson; K Calame
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

7.  Extinction of insulin gene expression in hybrids between beta cells and fibroblasts is accompanied by loss of the putative beta-cell-specific transcription factor IEF1.

Authors:  D Leshkowitz; M D Walker
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

8.  Extinction of Oct-3/4 gene expression in embryonal carcinoma x fibroblast somatic cell hybrids is accompanied by changes in the methylation status, chromatin structure, and transcriptional activity of the Oct-3/4 upstream region.

Authors:  E Ben-Shushan; E Pikarsky; A Klar; Y Bergman
Journal:  Mol Cell Biol       Date:  1993-02       Impact factor: 4.272

9.  Direct and indirect mechanisms of repression participate in suppression of T-cell-specific gene expression in T x L-cell hybrids.

Authors:  L Shurman; R Laskov; Y Bergman
Journal:  Gene Expr       Date:  1996

10.  Identification of a pancreatic beta-cell insulin gene transcription factor that binds to and appears to activate cell-type-specific expression: its possible relationship to other cellular factors that bind to a common insulin gene sequence.

Authors:  J Whelan; S R Cordle; E Henderson; P A Weil; R Stein
Journal:  Mol Cell Biol       Date:  1990-04       Impact factor: 4.272

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