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rdf:type |
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lifeskim:mentions |
umls-concept:C0012632,
umls-concept:C0013879,
umls-concept:C0013935,
umls-concept:C0015576,
umls-concept:C0017337,
umls-concept:C0026845,
umls-concept:C0043342,
umls-concept:C0086860,
umls-concept:C0596997,
umls-concept:C1704711,
umls-concept:C2266866
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pubmed:issue |
10
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pubmed:dateCreated |
1991-7-11
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pubmed:abstractText |
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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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2009862,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2108863,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2123467,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2133110,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2243772,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2311584,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2317864,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2501661,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2504586,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2550138,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2627887,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2632235,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2710114,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2725509,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2743976,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2769755,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2797000,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2806127,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2823106,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2828926,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2905426,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-2910853,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3036859,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3075543,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3119326,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3192074,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3194193,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3224553,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3336366,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3344222,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3405222,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3607873,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3785189,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-3816759,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-6548550,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-6888276,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2041743-6897014
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0305-1048
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
25
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2669-75
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:2041743-Actins,
pubmed-meshheading:2041743-Animals,
pubmed-meshheading:2041743-Base Sequence,
pubmed-meshheading:2041743-Binding, Competitive,
pubmed-meshheading:2041743-Cell Fractionation,
pubmed-meshheading:2041743-DNA,
pubmed-meshheading:2041743-DNA-Binding Proteins,
pubmed-meshheading:2041743-Molecular Sequence Data,
pubmed-meshheading:2041743-Multigene Family,
pubmed-meshheading:2041743-Muscle Development,
pubmed-meshheading:2041743-Nuclear Proteins,
pubmed-meshheading:2041743-Promoter Regions, Genetic,
pubmed-meshheading:2041743-Serum Response Factor,
pubmed-meshheading:2041743-Xenopus
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pubmed:year |
1991
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pubmed:articleTitle |
A family of muscle gene promoter element (CArG) binding activities in Xenopus embryos: CArG/SRE discrimination and distribution during myogenesis.
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pubmed:affiliation |
Department of Zoology, University of Cambridge, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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