An alternative, Nonkinase Product of the Brain-Specifically Expressed Ca2+/Calmodulin-Dependent Kinase II α Isoform Gene in Skeletal muscle
Author(s) -
K. Ulrich Bayer,
Jürgen Löhler,
Klaus Harbers
Publication year - 1996
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.16.1.29
Subject(s) - biology , gene isoform , exon , scn3a , alternative splicing , microbiology and biotechnology , gene product , gene , alpha (finance) , intron , skeletal muscle , rna splicing , g alpha subunit , protein kinase a , calmodulin , gene expression , rna , genetics , protein subunit , kinase , biochemistry , medicine , construct validity , nursing , patient satisfaction , enzyme , endocrinology
The gene for the alpha isoform of Ca2+/calmodulin-dependent kinase II (alpha CaMKII) codes for a multifunctional protein kinase that is found exclusively in the brain. Here we show that in skeletal muscle, an alternative nonkinase product, hereafter referred to as alpha KAP (alpha CaMKII association protein), is expressed from the same gene. alpha KAP consists of a C-terminal region that is identical to the association domain of alpha CaMKII, with the exception of 11 amino acids inserted in the variable region. The N-terminal sequence of alpha KAP is highly hydrophobic and not present in any known CaMKII protein. The catalytic and regulatory domains of alpha CaMKII are missing in alpha KAP. Analysis of the exon-intron structure revealed that the alpha KAP transcript is derived from the alpha CaMKII gene by alternative promoter usage and RNA splicing. The transcriptional start site of alpha KAP mRNA is located within an intron of the alpha CaMKII gene. Therefore, the relationship between alpha KAP and alpha CaMKII is that of a gene within a gene. Immunostaining using anti-alpha KAP antibodies suggests that alpha KAP is associated with sarcomeres of skeletal muscle fibers. On the basis of its primary structure and specific location, the possible function of alpha KAP as an anchoring protein for CaMKII is discussed.
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