Literature DB >> 3167985

Extinction of growth hormone expression in somatic cell hybrids involves repression of the specific trans-activator GHF-1.

A McCormick1, D Wu, J L Castrillo, S Dana, J Strobl, E B Thompson, M Karin.   

Abstract

Growth hormone (GH) expression in pituitary-derived cells has been attributed to the presence of a positive trans-activator, GHF-1, which binds to two sites on the GH promoter. Somatic cell hybridization of non-GH-expressing L cells with pituitary-derived GH3 cells usually results in extinction of GH production. While previous studies showed that extinction occurs at the level of GH transcription, the exact mechanism remained elusive. We therefore characterized two parental cell lines and three hybrids, two of which extinguish GH expression and one in which GH is reexpressed after loss of mouse chromosomal material. Using in vivo transfections, in vitro transcription, DNAase I footprints, and immunoblotting experiments, no evidence for a direct repressor of GH transcription was found. Rather, extinction of GH expression in fibroblast x pituitary hybrids was accompanied by loss of GHF-1 protein and mRNA expression, suggesting that extinction occurs by repression of this trans-activator.

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Year:  1988        PMID: 3167985     DOI: 10.1016/0092-8674(88)90061-x

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


  19 in total

1.  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

2.  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

3.  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

4.  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

5.  Hormonal regulation of TSE1-repressed genes: evidence for multiple genetic controls in extinction.

Authors:  M J Thayer; R E Fournier
Journal:  Mol Cell Biol       Date:  1989-07       Impact factor: 4.272

6.  Binding of a pancreatic nuclear protein is correlated with amylase enhancer activity.

Authors:  G Howard; P R Keller; T M Johnson; M H Meisler
Journal:  Nucleic Acids Res       Date:  1989-10-25       Impact factor: 16.971

7.  Hepatocyte nuclear factor-4 prevents silencing of hepatocyte nuclear factor-1 expression in hepatoma x fibroblast cell hybrids.

Authors:  G A Bulla
Journal:  Nucleic Acids Res       Date:  1997-06-15       Impact factor: 16.971

8.  Tse-2: a trans-dominant extinguisher of albumin gene expression in hepatoma hybrid cells.

Authors:  A C Chin; R E Fournier
Journal:  Mol Cell Biol       Date:  1989-09       Impact factor: 4.272

9.  Extinction and activation of the thyroglobulin promoter in hybrids of differentiated and transformed thyroid cells.

Authors:  I M Bonapace; M Sanchez; S Obici; A Gallo; S Garofalo; R Gentile; S Cocozza; E V Avvedimento
Journal:  Mol Cell Biol       Date:  1990-03       Impact factor: 4.272

10.  Selective disruption of growth hormone transcription machinery by viral infection.

Authors:  J C de la Torre; M B Oldstone
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

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