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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Biochemical and Biop...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Biochemical and Biophysical Research Communications
Article . 1997 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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Dog CREM Transcription Factors: Cloning, Tissue Distribution, and Identification of New Isoforms

Authors: Uyttersprot, Nathalie; Miot, Françoise;

Dog CREM Transcription Factors: Cloning, Tissue Distribution, and Identification of New Isoforms

Abstract

CREM (cAMP Response Element Modulator) transcription factors are involved in the cAMP-dependent transcriptional regulation of CRE-containing genes. Multiple CREM transactivators and repressors are generated from a single gene by alternative splicings and use of an alternative intronic promoter. Here we report the cloning and sequencing of the full-length dog CREM cDNA, corresponding to the CREMtau alpha splice variant. Amino acid sequence identity with mouse and human orthologs reached 94.5% and 91.0% respectively. Using the RNAse Protection Assay (RPA) method with three distinct probes, we analyzed the expression of the various CREM transcripts in several dog tissues. We showed that CREM transcription factors have a restricted tissue distribution and that the ratio between activators and repressors varies considerably from one tissue to another. Moreover, we amplified, by RT-PCR, a cDNA that corresponds to two new CREM isoforms and confirmed, by RPA experiments, the presence of these mRNAs in dog thyroid and in other tissues. These transcripts result from splicing of the gamma domain and encode potential CREM transactivators (CREMtau alphagamma and CREMtau2 alphagamma).

Country
Belgium
Keywords

DNA-Binding Proteins -- biosynthesis, DNA, Complementary, Molecular Sequence Data, Sequence Homology, Polymerase Chain Reaction, Promoter Regions, Cyclic AMP Response Element Modulator, Mice, Dogs, Genetic, Repressor Proteins -- biosynthesis, Complementary, Animals, Humans, Amino Acid Sequence, Cloning, Molecular, Promoter Regions, Genetic, DNA Primers, Base Sequence, Molecular, DNA-Binding Proteins -- analysis, DNA-Binding Proteins -- chemistry, DNA, Exons, Sciences bio-médicales et agricoles, Recombinant Proteins -- biosynthesis, Introns, Recombinant Proteins, DNA-Binding Proteins, Repressor Proteins, Repressor Proteins -- chemistry, Amino Acid, Alternative Splicing, Recombinant Proteins -- chemistry, Sequence Alignment, Thyroid Gland -- metabolism, Cloning

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
10
Average
Average
Average