Modularity in vertebrate brain development and evolution

被引:73
作者
Redies, C
Puelles, L
机构
[1] Univ Hosp Essen, Inst Anat, D-45122 Essen, Germany
[2] Univ Murcia, Fac Med, Dept Morphol Sci, E-30001 Murcia, Spain
关键词
D O I
10.1002/bies.10014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Embryonic modularity and functional modularity are two principles of brain organization. Embryonic modules are histogenetic fields that are specified by position-dependent expression of patterning genes. Within each embryonic module, secondary and higher-level pattern formation takes places during development, finally giving rise to brain nuclei and cortical layers. Defined subsets of these structures become connected by fiber tracts to form the information-processing neural circuits, which represent the functional modules of the brain. We review evidence that a group of cell adhesion molecules, the cadherins, provides an adhesive code for both types of modularity, based on a preferentially homotypic binding mechanism. Embryonic modularity is transformed into functional modularity, in part by translating early-generated positional information into an array of adhesive cues, which regulate the binding of functional neural structures distributed across the embryonic modules. Brain modularity may provide a basis for adaptability in evolution. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:1100 / 1111
页数:12
相关论文
共 100 条
[1]   Interneuron migration from basal forebrain to neocortex: Dependence on Dlx genes [J].
Anderson, SA ;
Eisenstat, DD ;
Shi, L ;
Rubenstein, JLR .
SCIENCE, 1997, 278 (5337) :474-476
[2]   Cadherin-defined segments and parasagittal cell ribbons in the developing chicken cerebellum [J].
Arndt, K ;
Nakagawa, S ;
Takeichi, M ;
Redies, C .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1998, 10 (5-6) :211-228
[3]  
Arndt K, 1996, J COMP NEUROL, V373, P373, DOI 10.1002/(SICI)1096-9861(19960923)373:3<373::AID-CNE5>3.0.CO
[4]  
2-#
[5]   PURIFIED N-CADHERIN IS A POTENT SUBSTRATE FOR THE RAPID INDUCTION OF NEURITE OUTGROWTH [J].
BIXBY, JL ;
ZHANG, R .
JOURNAL OF CELL BIOLOGY, 1990, 110 (04) :1253-1260
[6]   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
[7]   Slit proteins: key regulators of axon guidance, axonal branching, and cell migration [J].
Brose, K ;
Tessier-Lavigne, M .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (01) :95-102
[8]  
Cambronero F, 2000, J COMP NEUROL, V427, P522, DOI 10.1002/1096-9861(20001127)427:4<522::AID-CNE3>3.0.CO
[9]  
2-Y
[10]  
CLARKE JDW, 1993, DEVELOPMENT, V118, P151