Genetic analysis of ephrin-A2 and ephrin-A5 shows their requirement in multiple aspects of retinocollicular mapping

被引:367
作者
Feldheim, DA
Kim, YI
Bergemann, AD
Frisén, J
Barbacid, M
Flanagan, JG [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
[3] Med Noble Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
[4] Inst Salud Carlos III, Ctr Nacl Invest Oncol Carlos 3, Majadahonda 28220, Spain
关键词
D O I
10.1016/S0896-6273(00)81060-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ephrin-A2 and -A5 are thought to be anteroposterior mapping labels for the retinotectal/retinocollicular projection. Here, gene disruptions of both these ephrins are characterized. Focal retinal labeling reveals moderate map abnormalities when either gene is disrupted. Double heterozygotes also have a phenotype, showing an influence of absolute levels. In vitro assays indicate these ephrins are required for repellent activity in the target and also normal responsiveness in the retina. In double homozygotes, anteroposterior order is almost though not completely lost. Temporal or nasal retinal labelings reveal quantitatively similar but opposite shifts, with multiple terminations scattered widely over the target. These results indicate an axon competition mechanism for mapping, with a critical role for ephrins as anteroposterior topographic labels. Dorsoventral topography is also impaired, showing these ephrins are required in mapping both axes.
引用
收藏
页码:563 / 574
页数:12
相关论文
共 49 条
[1]   AXON GUIDANCE BY GRADIENTS OF A TARGET-DERIVED COMPONENT [J].
BAIER, H ;
BONHOEFFER, F .
SCIENCE, 1992, 255 (5043) :472-475
[2]   Graded and lamina-specific distributions of ligands of EphB receptor tyrosine kinases in the developing retinotectal system [J].
Braisted, JE ;
McLaughlin, T ;
Wang, HU ;
Friedman, GC ;
Anderson, DJ ;
OLeary, DDM .
DEVELOPMENTAL BIOLOGY, 1997, 191 (01) :14-28
[3]  
BRAMBILLA R, 1996, MOL CELL NEUROSCI, V8, P19
[4]   Characterization of the genes for mouse LERK-3/Ephrin-A3 (Epl3), mouse LERK-4/Ephrin-A4 (Epl4), and human LERK-6/Ephrin-A2 (EPLG6):: Conservation of intron/exon structure [J].
Cerretti, DP ;
Nelson, N .
GENOMICS, 1998, 47 (01) :131-135
[5]   ANTIFUNGAL ACTIVITY OF 2 XENORHABDUS SPECIES AND PHOTORHABDUS-LUMINESCENS, BACTERIA ASSOCIATED WITH THE NEMATODES STEINERNEMA SPECIES AND HETERORHABDITIS-MEGIDIS [J].
CHEN, G ;
DUNPHY, GB ;
WEBSTER, JM .
BIOLOGICAL CONTROL, 1994, 4 (02) :157-162
[6]   COMPLEMENTARY GRADIENTS IN EXPRESSION AND BINDING OF ELF-1 AND MEK4 IN DEVELOPMENT OF THE TOPOGRAPHIC RETINOTECTAL PROJECTION MAP [J].
CHENG, HJ ;
NAKAMOTO, M ;
BERGEMANN, AD ;
FLANAGAN, JG .
CELL, 1995, 82 (03) :371-381
[7]   EFFECTS OF BRAIN-DERIVED NEUROTROPHIC FACTOR ON OPTIC AXON BRANCHING AND REMODELING IN-VIVO [J].
COHENCORY, S ;
FRASER, SE .
NATURE, 1995, 378 (6553) :192-196
[8]   Expression and tyrosine phosphorylation of Eph receptors suggest multiple mechanisms in patterning of the visual system [J].
Connor, RJ ;
Menzel, P ;
Pasquale, EB .
DEVELOPMENTAL BIOLOGY, 1998, 193 (01) :21-35
[9]   MURINE FGFR-1 IS REQUIRED FOR EARLY POSTIMPLANTATION GROWTH AND AXIAL ORGANIZATION [J].
DENG, CX ;
WYNSHAWBORIS, A ;
SHEN, MM ;
DAUGHERTY, C ;
ORNITZ, DM ;
LEDER, P .
GENES & DEVELOPMENT, 1994, 8 (24) :3045-3057
[10]   The Eph kinase ligand AL-1 is expressed by rostral muscles and inhibits outgrowth from caudal neurons [J].
Donoghue, MJ ;
Lewis, RM ;
Merlie, JP ;
Sanes, JR .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1996, 8 (2-3) :185-198