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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1990-3-28
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J05240,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M31104,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M31105,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32726,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32727,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32728,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32729,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32730,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32731,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32732
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pubmed:abstractText |
The structure of the 42-kilobase (kb) long chicken progesterone receptor (cPR) gene and of all six transcripts that are detectable on Northern blots was determined. The first of 8 exons encodes the N-terminal region A/B which is highly divergent among different species and contains a constitutive transcription activation function. The DNA (DBD)- and hormone-binding domains (HBD) are assembled from 2 and 5 exons, respectively, with the individual "zinc fingers" of the DBD encoded by separate exons. In addition to the previously described 4.5-kb cPR mRNA species, alternative polyadenylation, splicing variation, and "5'-truncation" lead to the generation of 5 further mRNAs. Most importantly, this 5'-truncation produces, by an as yet unidentified mechanism, an abundant transcript which encodes form A but not form B of cPR. Lack of splicing at the exon 2 splice-donor and polyadenylation due to a signal site in the second intron generates a previously undetected 3.4-kb mRNA species. The corresponding cDNA was sequenced in its entirety and shown to encode only region A/B and the N-terminal "finger" of the DBD. Alternative polyadenylation upstream of the signal site for the 4.5-kb mRNA is responsible for the appearance of a 3.3-kb mRNA. The longest cPR mRNA (8.2 kb) originates from a transcription termination point more than 3 kb downstream of the 4.5-kb mRNA 3'-end. Finally, the primary sequence of more than 2 kb upstream sequences of the cPR gene, containing several consensus hexamer progestin/glucocorticoid receptor-binding sites (PRE/GRE and putative Sp1 binding motifs, is discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
5
|
pubmed:volume |
265
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3967-74
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2303488-Amino Acid Sequence,
pubmed-meshheading:2303488-Animals,
pubmed-meshheading:2303488-Base Sequence,
pubmed-meshheading:2303488-Blotting, Northern,
pubmed-meshheading:2303488-Cell Nucleus,
pubmed-meshheading:2303488-Chickens,
pubmed-meshheading:2303488-DNA,
pubmed-meshheading:2303488-Exons,
pubmed-meshheading:2303488-Genes,
pubmed-meshheading:2303488-Genetic Variation,
pubmed-meshheading:2303488-Molecular Sequence Data,
pubmed-meshheading:2303488-RNA, Messenger,
pubmed-meshheading:2303488-RNA Splicing,
pubmed-meshheading:2303488-Receptors, Progesterone,
pubmed-meshheading:2303488-Restriction Mapping,
pubmed-meshheading:2303488-Sequence Homology, Nucleic Acid,
pubmed-meshheading:2303488-Transcription, Genetic
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pubmed:year |
1990
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pubmed:articleTitle |
Characterization of multiple mRNAs originating from the chicken progesterone receptor gene. Evidence for a specific transcript encoding form A.
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pubmed:affiliation |
Laboratoire de Génétique Moléculaire des Eucaryotes du Centre National de la Recherche Scientifique, Faculté de Médicine, Strasbourg, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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