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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1996-3-5
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pubmed:abstractText |
Development of murine proximal colon follows a complex pattern of morphological and functional differentiation. Molecular mechanisms and factors responsible for colon-specific gene expression remain to be established. In an attempt to identify some of these factors, we examined the expression of the alpha, beta, and delta isoforms of the CCAAT/enhancer binding protein (C/EBP) transcription factor gene family during murine colon development. Whereas C/EBP alpha mRNA levels are reduced during the third post-natal week, C/EBP alpha 42 and 30 kD proteins levels decrease between post-natal days 8 and 21. C/EBP beta mRNA levels increase between post-natal days 4 and 8 and remain constant subsequently, in contrast to a decrease in C/EBP beta protein levels between post-natal days 11 and 15. C/EBP delta mRNA levels increase gradually while C/EBP delta protein levels show variations during post-natal development. Changes in C/EBP DNA binding activity coincides with modifications in C/EBP isoforms expression. By indirect immunofluorescence, we show restriction of C/EBP alpha expression to differentiated surface epithelial cells during crypt formation. C/EBP alpha is predominantly nuclear with some cytoplasmic staining at all developmental stages. C/EBP beta and delta are both predominantly nuclear in crypt and differentiated surface epithelial cells, as well as in various cells of the lamina propria and muscular layers. Thus, specific C/EBP isoforms are differentially regulated during murine colon post-natal development. Differential C/EBP isoforms pattern of expression suggests a role for these transcription factors in colon-specific gene expression during development.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCAAT-Enhancer-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1058-8388
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
204
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
66-76
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8563027-Animals,
pubmed-meshheading:8563027-Animals, Newborn,
pubmed-meshheading:8563027-Base Sequence,
pubmed-meshheading:8563027-CCAAT-Enhancer-Binding Proteins,
pubmed-meshheading:8563027-Colon,
pubmed-meshheading:8563027-DNA-Binding Proteins,
pubmed-meshheading:8563027-Enhancer Elements, Genetic,
pubmed-meshheading:8563027-Gene Expression Regulation, Developmental,
pubmed-meshheading:8563027-Immunohistochemistry,
pubmed-meshheading:8563027-Isomerism,
pubmed-meshheading:8563027-Mice,
pubmed-meshheading:8563027-Mice, Inbred ICR,
pubmed-meshheading:8563027-Molecular Sequence Data,
pubmed-meshheading:8563027-Nuclear Proteins,
pubmed-meshheading:8563027-RNA, Messenger,
pubmed-meshheading:8563027-Transcription Factors
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pubmed:year |
1995
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pubmed:articleTitle |
CCAAT/enhancer binding protein isoforms expression in the colon of neonatal mice.
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pubmed:affiliation |
Département d'Anatomie et Biologie Cellulaire, Faculté de Médecine, Université de Sherbrooke, Québec, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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