Literature DB >> 7610053

DNase I-hypersensitive sites in the chromatin of rat growth hormone gene locus and enhancer activity of regions with these sites.

A Aizawa1, T Yoneyama, K Kazahari, M Ono.   

Abstract

In this study, a determination was made of the chromatin structure of the rat growth hormone (GH) gene locus by DNase I sensitivity analysis using GC [GH+, prolactin (PRL)-], 235 (GH-, PRL+), GH3 (GH+, PRL+) and liver (GH-, PRL-) cells. From 7 kb upstream from the transcription start site to 19 kb downstream from the polyadenylation site, two major DNase I-hypersensitive sites (M-DHS; UIA, UIIA) and three M-DHS (DIA, DII, DIII) were found within 2 kb upstream and 7 kb downstream regions, respectively. Two minor DHS (m-DHS; UIB, UIIB) in the upstream region and one m-DHS (DIB) downstream were shown to be associated with M-DHS. Thus, a total of five M-DHS and three m-DHS were mapped on the rat GH gene locus. Among these, five (UIIB, UIA, UIB, DIB, DIA) including two (UIA, DIA) M-DHS were specific for GH-producing cells. UIIA and DIII were M-DHS only in PRL-producing 235 cells while the major hypersensitivity of DII was detected in GH-producing cells and liver cells. Assessment of the enhancing activity of the DHS regions indicated novel enhancers in one upstream and two downstream regions that function well with the GH promoter in GC cells. These enhancers, each appearing different, coincided with m-DHS but not M-DHS in GC cells, and were not activated by Pit-1. Based on these observations, the following functions of five M-DHS and three m-DHS regions were defined: enhancer; locus control region (LCR); switch region serving for conversion from GH/PRL-producing cells to PRL-producing cells; and a region having a structural function in chromatin.

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Year:  1995        PMID: 7610053      PMCID: PMC307013          DOI: 10.1093/nar/23.12.2236

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  46 in total

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Authors:  Y G Watanabe; S Daikoku
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2.  Analysis of hypersensitive sites in chromatin.

Authors:  C Wu
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Authors:  F C Bancroft
Journal:  Endocrinology       Date:  1973-04       Impact factor: 4.736

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Authors:  W L Miller; N L Eberhardt
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Authors:  T D Sargent; L L Jagodzinski; M Yang; J Bonner
Journal:  Mol Cell Biol       Date:  1981-10       Impact factor: 4.272

6.  Nucleotide sequence of cloned rat serum albumin messenger RNA.

Authors:  T D Sargent; M Yang; J Bonner
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

7.  Ontogeny of prolactin cells in neonatal rats: initial prolactin secretors also release growth hormone.

Authors:  J P Hoeffler; F R Boockfor; L S Frawley
Journal:  Endocrinology       Date:  1985-07       Impact factor: 4.736

8.  A new clonal strain of rat pituitary tumour cells: a model for non-regulated secretion of prolactin.

Authors:  M J Reymond; D D Nansel; G H Burrows; W B Neaves; J C Porter
Journal:  Acta Endocrinol (Copenh)       Date:  1984-08

9.  Ontogenesis of cells producing polypeptide hormones (ACTH, MSH, LPH, GH, prolactin) in the fetal hypophysis of the rat: influence of the hypothalamus.

Authors:  A Chatelain; J P Dupouy; M P Dubois
Journal:  Cell Tissue Res       Date:  1979-02-28       Impact factor: 5.249

10.  Chromatin structure, transcription, and methylation of the prolactin gene domain in pituitary tumors of Fischer 344 rats.

Authors:  L K Durrin; J L Weber; J Gorski
Journal:  J Biol Chem       Date:  1984-06-10       Impact factor: 5.157

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  1 in total

1.  Genomic analysis of the mouse protamine 1, protamine 2, and transition protein 2 gene cluster reveals hypermethylation in expressing cells.

Authors:  Y C Choi; A Aizawa; N B Hecht
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  1 in total

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