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Publication : Mouse C-reactive protein. Generation of cDNA clones, structural analysis, and induction of mRNA during inflammation.

First Author  Whitehead AS Year  1990
Journal  Biochem J Volume  266
Issue  1 Pages  283-90
PubMed ID  2310378 Mgi Jnum  J:10359
Mgi Id  MGI:58811 Doi  10.1042/bj2660283
Citation  Whitehead AS, et al. (1990) Mouse C-reactive protein. Generation of cDNA clones, structural analysis, and induction of mRNA during inflammation. Biochem J 266(1):283-90
abstractText  A full-length C-reactive protein (CRP) cDNA clone has been isolated from a CBA/J-strain-mouse acute-phase liver library. The 1614-nucleotide cDNA specifies mRNA 5' and 3' untranslated regions of 81 and 858 bases respectively that flank 675 bases encoding mouse pre-CRP. The derived amino acid sequence predicts a 19-residue leader peptide followed by a 206-residue mature mouse CRP that shows considerable sequence identity with both human and rabbit CRP. Northern-blot analysis of mouse liver CRP mRNA concentrations after inflammatory stimuli and comparison with hepatic induction of mRNA for the major mouse acute-phase protein serum amyloid P component established that CRP, a major acute-phase reactant in human and rabbit, is a minor acute-phase reactant in mouse. The size and organization of the mouse CRP mRNA 5' and 3' untranslated regions are significantly different from those of human and rabbit CRP mRNA and may have implications for its anomalous minimal induction during acute inflammation.
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