Literature DB >> 1316911

Positive and negative regulatory DNA elements including a CCArGG box are involved in the cell type-specific expression of the human muscle dystrophin gene.

H Gilgenkrantz1, J P Hugnot, M Lambert, P Chafey, J C Kaplan, A Kahn.   

Abstract

The muscle-specific promoter of the dystrophin gene is active in skeletal, cardiac, and smooth muscles and is specifically stimulated during differentiation of myoblasts into multinucleated myotubes. An 850-base pair (bp) DNA fragment upstream from the cap site is able to confer a partial muscle specificity to a reporter gene. The region between -850 and -140 bp includes nonspecific negative and positive regulatory sequences. A continuous stretch of 140 bp upstream from the cap site exhibits a striking conservation between rodents and human (93% homology) and still retains muscle preference of expression. It contains two putative binding sites for factors involved in regulation of other muscle-specific genes, a CCArGG box and an E box. This latter element, however, is unable to confer the ability to be transactivated by MyoD1 to the dystrophin promoter. The -140-bp promoter fragment exhibits antagonist effects contributed by one inhibiting sequence (nucleotide -140/-96), active in all cell types, and one activating region, from nucleotide -96 to the cap site, sufficient to confer a muscle preference of expression, in which the CCArGG box seems to play a major role.

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Year:  1992        PMID: 1316911

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  10 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-09-25       Impact factor: 16.971

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-10-11       Impact factor: 16.971

3.  A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs.

Authors:  H J Klamut; L O Bosnoyan-Collins; R G Worton; P N Ray
Journal:  Nucleic Acids Res       Date:  1997-04-15       Impact factor: 16.971

4.  Growth and differentiation of C2 myogenic cells are dependent on serum response factor.

Authors:  M Soulez; C G Rouviere; P Chafey; D Hentzen; M Vandromme; N Lautredou; N Lamb; A Kahn; D Tuil
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

5.  Striking conservation of the brain-specific region of the dystrophin gene.

Authors:  J P Hugnot; H Gilgenkrantz; M Jeanpierre; J Chelly; J C Kaplan; A Kahn
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

6.  Soybean nodulin-26 gene encoding a channel protein is expressed only in the infected cells of nodules and is regulated differently in roots of homologous and heterologous plants.

Authors:  G H Miao; D P Verma
Journal:  Plant Cell       Date:  1993-07       Impact factor: 11.277

7.  hMEF2C gene encodes skeletal muscle- and brain-specific transcription factors.

Authors:  J C McDermott; M C Cardoso; Y T Yu; V Andres; D Leifer; D Krainc; S A Lipton; B Nadal-Ginard
Journal:  Mol Cell Biol       Date:  1993-04       Impact factor: 4.272

8.  Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.

Authors:  F Muntoni; M A Melis; A Ganau; V Dubowitz
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

9.  Serum response factor and protein-mediated DNA bending contribute to transcription of the dystrophin muscle-specific promoter.

Authors:  F Galvagni; M Lestingi; E Cartocci; S Oliviero
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

10.  Localization of dystrophin gene transcripts during mouse embryogenesis.

Authors:  D Houzelstein; G E Lyons; J Chamberlain; M E Buckingham
Journal:  J Cell Biol       Date:  1992-11       Impact factor: 10.539

  10 in total

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