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Identification of the Isoforms of Ca 2+ /Calmodulin‐Dependent Protein Kinase II in Rat Astrocytes and Their Subcellular Localization
Author(s) -
Takeuchi Yusuke,
Yamamoto Hideyuki,
Fukunaga Kohji,
Miyakawa Taihei,
Miyamoto Eishichi
Publication year - 2000
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2000.0742557.x
Subject(s) - gene isoform , subcellular localization , nuclear localization sequence , golgi apparatus , biology , microbiology and biotechnology , calmodulin , cell nucleus , kinase , protein kinase a , immunostaining , protein kinase c , nucleus , biochemistry , cytoplasm , gene , endoplasmic reticulum , enzyme , immunohistochemistry , immunology
Ca 2+ /calmodulin‐dependent protein kinase II (CaM kinase II) occurs in astrocytes as well as in neurons in brain. We have reported that CaM kinase II is involved in the regulation of cytoskeletal proteins and gene expression in astrocytes. In this study, we identified all isoforms of CaM kinase II in astrocytes and examined their subcellular localization. When we amplified the isoforms of four subunits by RT‐PCR followed by the “nested” PCR, totally 10 isoforms were obtained. Immunoblot analyses with five types of antibodies against CaM kinase II indicated that the most abundant isoform was δ2. Immunostaining suggested that the δ2 isoform was localized predominantly at the Golgi apparatus. The localization of the δ2 isoform at the Golgi apparatus was also observed in NG108‐15 cells. We overexpressed all isoforms that contained the nuclear localization signal to examine their nuclear targeting in NG108‐15 cells. In contrast to the αB and δ3 isoforms that entered the nucleus, as reported, the γA isoform was excluded from the nucleus in the transfected NG108‐15 cells. These results suggest that the 15‐amino acid insertion following the nuclear localization signal inhibits the nuclear targeting of the γA isoform.