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Publication : Molecular cloning and expression analysis of rat Rgs12 and Rgs14.

First Author  Snow BE Year  1997
Journal  Biochem Biophys Res Commun Volume  233
Issue  3 Pages  770-7
PubMed ID  9168931 Mgi Jnum  J:40212
Mgi Id  MGI:87554 Doi  10.1006/bbrc.1997.6537
Citation  Snow BE, et al. (1997) Molecular cloning and expression analysis of rat Rgs12 and Rgs14. Biochem Biophys Res Commun 233(3):770-7
abstractText  We report the cloning of two novel rat regulators of G- protein signaling (RGS) cDNAs using a degenerate PCR strategy. The rRgs12 and rRgs14 cDNAs encode predicted polypeptides of 1387 and 544 amino acids, respectively, We have also identified the human orthologue of rRgs12 by alignment of cosmid sequences in the database which map the human RGS12 gene to chromosome 4p16.3. Furthermore, we identified human ESTs with high homology to rRgs14 which map to human chromosome 5qter. Northern blot analysis indicates that rRgs14 is expressed at high levels in brain, lung, and spleen, whereas rRgs12 is expressed at high levels in brain and lung and lower levels in testis, heart, and spleen. Analysis of the predicted rRGS12 and rRGS14 polypeptides indicates that they are closely related and possess regions of homology outside of the conserved RGS domain. We have also identified conserved regions in RGS12 which are similar to protein domains found in mouse rhophilin and coiled-coil proteins suggesting possible interactions with ras-like G-proteins. (C) 1997 Academic Press.
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