ArticleNucleic acids research1991
A family of muscle gene promoter element (CArG) binding activities in Xenopus embryos: CArG/SRE discrimination and distribution during myogenesis.
Article in Nucleic acids research, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 23 citations in OpenAlex.
- Identification of novel tropomyosin 1 genes of pufferfish (Fugu rubripes) on genomic sequences and tissue distribution of their transcripts.Molecular biology reports · 2003Article
- Growth and differentiation of C2 myogenic cells are dependent on serum response factor.Molecular and cellular biology · 1996Article
- Developmental stage-specific regulation of atrial natriuretic factor gene transcription in cardiac cells.Molecular and cellular biology · 1994Article
- Functional and defective components of avian endogenous virus long terminal repeat enhancer sequences.Journal of virology · 1993Article
- Activation of a muscle-specific actin gene promoter in serum-stimulated fibroblasts.Molecular biology of the cell · 1992Article
- Serum response factor p67SRF is expressed and required during myogenic differentiation of both mouse C2 and rat L6 muscle cell lines.The Journal of cell biology · 1992Article
- CArG, CCAAT, and CCAAT-like protein binding sites in avian retrovirus long terminal repeat enhancers.Journal of virology · 1992Article
- Natural and synthetic DNA elements with the CArG motif differ in expression and protein-binding properties.Molecular and cellular biology · 1991Article
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Authors and funding
1 author at 1 institution in 1 country.
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Abstract
The CArG box is an essential promoter sequence for cardiac muscle actin gene expression in Xenopus embryos. To assess the role of the CArG motif in promoter function during Xenopus development, the DNA-binding activities present in the embryo that interact with this sequence have been investigated. A family of four Embryo CArG box1 Factors (ECFs) was separated by a 2-step fractionation procedure. These factors were distinct from the previously described C-ArG box binding activity Serum Response Factor (SRF). ECF1 was the most prominent binding activity in cardiac actin-expressing tissues, and bound the CArG box in preference to a Serum Response Element (SRE). SRF was also detectable in muscle, but it bound preferentially to an SRE. The properties of ECF3 were similar to those of ECF1, but it was much less prominent in cardiac actin-expressing tissues. The properties of the two other factors were distinctive: ECF2 was of relatively low affinity and high abundance, whilst ECF4 bound non-specifically to ends of DNA. The binding activity (or activities) that interacted with the CArG box was found to be influenced by both the concentrations of the other CArG box binding activities and the sequence of the site. Although there was no evidence for a muscle-specific CArG box binding activity, the properties of ECF1 suggest that it could play a role in the expression of the cardiac actin gene during Xenopus development.
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