A truncated isoform of Ca2+/calmodulin-dependent protein kinase II expressed in human islets of Langerhans may result from trans-splicing

被引:25
作者
Breen, MA [1 ]
Ashcroft, SJH [1 ]
机构
[1] JOHN RADCLIFFE HOSP,NUFFIELD DEPT CLIN BIOCHEM,OXFORD OX3 9DU,ENGLAND
基金
英国医学研究理事会; 英国惠康基金;
关键词
CaM kinase II; signal recognition particle; trans-splicing; pancreatic beta-cell; human islets of Langerhans; protein phosphorylation;
D O I
10.1016/S0014-5793(97)00555-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calcium/calmodulin-dependent protein kinase II (CaM kinase II) has been proposed to play a key role in glucose stimulated insulin secretion, Using the rapid amplification of cDNA ends technique we amplified the 3' end of the CaM kinase II gamma gene from human islet RNA, A novel cDNA was detected composed of 5' sequence from the human CaM kinase II gamma gene joined to the 3' end of the human signal recognition particle 72 (SRP72) gene. We predict that this mRNA species will code for a truncated form of CaM kinase II, designated gamma(SRP), comprising the entire catalytic and regulatory domains of the protein and with a predicted molecular weight of 37 kDa. We mapped the human SRP72 gene to chromosome 18 and, as the CaM kinase II gamma gene was previously mapped to human chromosome 10q22, we suggest this novel cDNA may have resulted from transsplicing. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:375 / 379
页数:5
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