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Publication : Molecular cloning and characterization of mouse cardiac triadin isoforms.

First Author  Hong CS Year  2001
Journal  Gene Volume  278
Issue  1-2 Pages  193-9
PubMed ID  11707337 Mgi Jnum  J:72914
Mgi Id  MGI:2153979 Doi  10.1016/s0378-1119(01)00718-1
Citation  Hong CS, et al. (2001) Molecular cloning and characterization of mouse cardiac triadin isoforms. Gene 278(1-2):193-9
abstractText  Triadin is a ryanodine receptor and calsequestrin binding protein located in junctional sarcoplasmic reticulum of striated muscles. In the present study, mouse cardiac triadin cDNAs have been identified by cDNA library screening and RT-PCR. The deduced aa sequences show that the three isoforms consist of 277, 293 and 305 aa giving rise to the molecular weights of approximately 31,414, 33,066, and 34,328, respectively. The isoforms have identical 262 aa N-terminal sequences, whereas they have distinct C-terminal sequences. Northern blot analysis using a cDNA probe representing the N-terminal common region of triadin revealed that the mouse triadins were present both in heart and skeletal muscles. The estimated sizes of the transcripts were approximately 1.3, 4.3 and 5 kb in heart and 5, 5.5 and 7 kb in skeletal muscle. Endo H treatment and Western blot analysis of isolated mouse cardiac sarcoplasmic reticulum and in vitro translation products indicate that there are three distinct mouse cardiac triadin isoforms having molecular weights of 35, 35.5 and 40 kDa. We termed those three isoforms as mouse cardiac triadin 1, mouse cardiac triadin 2 and mouse cardiac triadin 3.
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