The cadherin-related neuronal receptor family: a novel diversified cadherin family at the synapse

被引:32
作者
Hamada, S
Yagi, T
机构
[1] Osaka Univ, Inst Mol & Cellular Biol, Div Mol Genet, Suita, Osaka 5650871, Japan
[2] Natl Inst Physiol Sci, Lab Neurobiol & Behav Genet, Okazaki, Aichi 4448585, Japan
关键词
cadherin-related neuronal receptor; cadherin; protocadherin; synapse; synapse formation; gene cluster;
D O I
10.1016/S0168-0102(01)00281-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The cadherin-related neuronal receptor (CNR) family has been identified as a receptor family that cooperates with Fyn, a member of the Src family of tyrosine kinases. The CNR family is composed of 14 members in mice and 15 members in humans. The mRNAs of CNR s are highly expressed in the brain and CNR1 protein is localized at synaptic junctions. Hence CNR family proteins are synaptic cadherins. The unique structure of CNR family cDNAs, which is characterized by complete DNA sequence identity among their 3'-termini including a part of the coding region, prompted us to investigate the genomic organization of this family. The genomic organization of CNRs is divided into 'variable' and 'constant' region exons, analogous to immunoglobulin and T cell receptor gene clusters. This organization raised the possibility that the CNR gene cluster may undergo somatic DNA rearrangement or trans-splicing and produce diversified gene products. Although it is not yet clear that the CNR gene cluster in the neuronal genomic DNA is somatically changed, a recent study suggested the occurrence of trans-transcripts and accumulation of somatic mutations in CNR transcripts (Genes Cells 6 (2001) 151). These results suggested that the proteins from the CNR gene cluster are enormously diversified by unique mechanisms. The localization of CNR1 protein at the synapse and the diversity of CNRs led us to the hypothesis that gene regulation of the CNR family dictates the formation and reorganization of synaptic connections in the nervous system. (C) 2001 Elsevier Science Ireland Ltd. and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:207 / 215
页数:9
相关论文
共 55 条
[1]  
AGHAJANIAN G. K., 1967, BRAIN RES, V6, P716, DOI 10.1016/0006-8993(67)90128-X
[2]   MATURATION OF THE IMMUNE-RESPONSE IN GERMINAL-CENTERS [J].
BEREK, C ;
BERGER, A ;
APEL, M .
CELL, 1991, 67 (06) :1121-1129
[3]   Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain [J].
Blanco, P ;
Sargent, CA ;
Boucher, CA ;
Mitchell, M ;
Affara, NA .
MAMMALIAN GENOME, 2000, 11 (10) :906-914
[4]   Increasing numbers of synaptic puncta during late-phase LTP: N-cadherin is synthesized, recruited to synaptic sites, and required for potentiation [J].
Bozdagi, O ;
Shan, W ;
Tanaka, H ;
Benson, DL ;
Huntley, GW .
NEURON, 2000, 28 (01) :245-259
[5]   Juxtaposition of CNR protocadherins and reelin expression in the developing spinal cord [J].
Carroll, P ;
Gayet, O ;
Feuillet, C ;
Kallenbach, S ;
de Bovis, B ;
Dudley, K ;
Alonso, S .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2001, 17 (04) :611-623
[6]   A PROTEIN RELATED TO EXTRACELLULAR-MATRIX PROTEINS DELETED IN THE MOUSE MUTANT REELER [J].
DARCANGELO, G ;
MIAO, GG ;
CHEN, SC ;
SOARES, HD ;
MORGAN, JI ;
CURRAN, T .
NATURE, 1995, 374 (6524) :719-723
[7]   A model for central synaptic junctional complex formation based on the differential adhesive specificities of the cadherins [J].
Fannon, AM ;
Colman, DR .
NEURON, 1996, 17 (03) :423-434
[8]   IMPAIRED LONG-TERM POTENTIATION, SPATIAL-LEARNING, AND HIPPOCAMPAL DEVELOPMENT IN FYN MUTANT MICE [J].
GRANT, SGN ;
ODELL, TJ ;
KARL, KA ;
STEIN, PL ;
SORIANO, P ;
KANDEL, ER .
SCIENCE, 1992, 258 (5090) :1903-1910
[9]   Somatic mutations of synaptic cadherin (CNR family) transcripts in the nervous system [J].
Hirayama, T ;
Sugino, H ;
Yagi, T .
GENES TO CELLS, 2001, 6 (02) :151-164
[10]  
Inoue T, 1998, DEV DYNAM, V211, P338, DOI 10.1002/(SICI)1097-0177(199804)211:4<338::AID-AJA5>3.0.CO