Developmental expression in the mouse nervous system of the p49(3F12) SAP kinase

被引:111
作者
Martin, JH
Mohit, AA
Miller, CA
机构
[1] UNIV SO CALIF,SCH MED,DEPT PATHOL,LOS ANGELES,CA 90033
[2] UNIV SO CALIF,SCH MED,DEPT NEUROL,LOS ANGELES,CA 90033
[3] UNIV SO CALIF,SCH MED,PROGRAM NEUROSCI,LOS ANGELES,CA 90033
来源
MOLECULAR BRAIN RESEARCH | 1996年 / 35卷 / 1-2期
关键词
MAP kinase; neuron specificity; neuronal development; stress-activated protein kinase beta; synaptogenesis; neuroblastoma;
D O I
10.1016/0169-328X(95)00181-Q
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mitogen-activated protein (MAP) kinases are proline-directed, serine/threonine kinases that respond to a variety of extracellular signals. A subgroup of these kinases, stress-activated protein (SAP) kinases, phosphorylate c-jun in response to cellular stress. Using monoclonal antibody (MAb) 3F12, we have cloned and partially characterized p49(3F12) kinase, a mouse homologue of the rat SAP beta kinase and described its expression in the adult and developing mouse. Unlike previously reported MAP and SAP kinases, it is primarily expressed as a 2.7 kb transcript in neurons in the nervous system of the adult mouse. A 2.4 kb transcript is also expressed in the testis. Immunocytochemically, MAb 3F12 decorates a loop-like structure encircling the nucleus in the cytoplasm of neurons in the adult brain, and distinct perinuclear dots in the embryos. In situ hybridization first reveals expression in post-mitotic neurons, on embryonic day 11. The mRNA is also expressed in the Neuro-2A neuroblastoma cell line and is not upregulated in response to differentiating agents. The neuronal specificity of this kinase suggests the presence of a signal transduction cascade unique to neurons. As the amino acid sequence is highly conserved in the human and mouse, the latter may serve as a model for regulation and expression of this kinase.
引用
收藏
页码:47 / 57
页数:11
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