MOLECULAR-CLONING OF RAT CDNAS FOR BETA-SUBTYPE AND GAMMA-SUBTYPE OF 14-3-3 PROTEIN AND DEVELOPMENTAL-CHANGES IN EXPRESSION OF THEIR MESSENGER-RNAS IN THE NERVOUS-SYSTEM

被引:70
作者
WATANABE, M
ISOBE, T
ICHIMURA, T
KUWANO, R
TAKAHASHI, Y
KONDO, H
机构
[1] TOHOKU UNIV,SCH MED,DEPT ANAT,SENDAI,MIYAGI 980,JAPAN
[2] TOKYO METROPOLITAN UNIV,FAC SCI,DEPT CHEM,TOKYO 158,JAPAN
[3] NIIGATA UNIV,GRAD SCH SCI & TECHNOL,DEPT BIOSYST SCI,NIIGATA 95021,JAPAN
[4] NIIGATA UNIV,MOLEC GENET RES LAB,NIIGATA 95021,JAPAN
来源
MOLECULAR BRAIN RESEARCH | 1993年 / 17卷 / 1-2期
关键词
14-3-3; PROTEIN; BETA-SUBTYPE; GAMMA-SUBTYPE; BRAIN; CDNA CLONING; INSITU HYBRIDIZATION; NORTHERN BLOT; DEVELOPMENT; RAT;
D O I
10.1016/0169-328X(93)90082-Z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We isolated cDNAs to beta and gamma subtypes of 14-3-3 protein, a putative regulatory protein for protein kinase C, from the brain and clarified a high homology in sequences of nucleotides and deduced amino acids between the two rat subtypes and the bovine counterparts and even reciprocally between the two rat subtypes. In Northern blot analysis, the gene expression of the two subtypes was detected weakly at E13, increased progressively after birth and reached a maximum at P7-P14. Thereafter it decreased slightly. In situ hybridization analysis allowed detection of the beta but not the gamma subtype in the matrix cells of the ventricular germinal zone of the neural wall. In post-mitotic neurons in the mantle zone and maturing brain loci, genes of the two subtypes were expressed in patterns similar to each other, and three neuron types were identified: type I neurons with high levels of expression throughout development; type II neurons showing high expression during the early developmental stages with a subsequent decrease in the expression at maturing and adult stages; and type III neurons showing consistently low levels of expression throughout development. The wider and more highly-patterned expression of the 14-3-3 protein family than expected suggests that this protein may be involved in the elaborate regulation of some fundamental cellular activities and differentiation of neurons.
引用
收藏
页码:135 / 146
页数:12
相关论文
共 30 条
[2]  
ASE K, 1988, J NEUROSCI, V8, P3850
[4]  
BERRY M, 1965, J ANAT, V99, P691
[5]   HUMAN 14-3-3 PROTEIN - RADIOIMMUNOASSAY, TISSUE DISTRIBUTION, AND CEREBROSPINAL-FLUID LEVELS IN PATIENTS WITH NEUROLOGICAL DISORDERS [J].
BOSTON, PF ;
JACKSON, P ;
THOMPSON, RJ .
JOURNAL OF NEUROCHEMISTRY, 1982, 38 (05) :1475-1482
[6]  
BRADT SJ, 1987, CELL, V49, P57
[7]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335
[8]   DEVELOPMENTAL EXPRESSION OF PROTEIN KINASE-C ISOZYMES IN RAT CEREBELLUM [J].
HUANG, FL ;
YOUNG, WS ;
YOSHIDA, Y ;
HUANG, KP .
DEVELOPMENTAL BRAIN RESEARCH, 1990, 52 (1-2) :121-130
[9]   WIDESPREAD DISTRIBUTION OF THE 14-3-3 PROTEIN IN VERTEBRATE BRAINS AND BOVINE-TISSUES - CORRELATION WITH THE DISTRIBUTIONS OF CALCIUM-DEPENDENT PROTEIN-KINASES [J].
ICHIMURA, T ;
SUGANO, H ;
KUWANO, R ;
SUNAYA, T ;
OKUYAMA, T ;
ISOBE, T .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (04) :1449-1451
[10]   MOLECULAR-CLONING OF CDNA CODING FOR BRAIN-SPECIFIC 14-3-3 PROTEIN, A PROTEIN KINASE-DEPENDENT ACTIVATOR OF TYROSINE AND TRYPTOPHAN HYDROXYLASES [J].
ICHIMURA, T ;
ISOBE, T ;
OKUYAMA, T ;
TAKAHASHI, N ;
ARAKI, K ;
KUWANO, R ;
TAKAHASHI, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7084-7088