TY - JOUR
T1 - Axon patterning requires DN-cadherin, a novel neuronal adhesion receptor, in the drosophila embryonic CNS
AU - Iwai, Youichi
AU - Usui, Tadao
AU - Hirano, Shinji
AU - Steward, Ruth
AU - Takeichi, Masatoshi
AU - Uemura, Tadashi
N1 - Funding Information:
The authors would like to thank M. Bate, S. Hayashi, T. Hosoya, Y. Hotta, T. Isshiki, L. Luo, A. Nose, B. Thisse, and especially J. Thomas for strains; M. Peifer, G. Technau, and in particular C. Goodman for antibodies; M. Iwami, H. Kokubo, K. Ohno, and Y. Suzuki for Bombyx cDNA libraries; and H. Ohkura for a cosmid clone that hybridizes with the D N-cadherin cDNA. We are grateful to M. Murata, S. Saito, and M. Yanagida for giving us opportunities to use their confocal microscopes; and members of A. Nose's group for allowing us to perform microinjection in their laboratory. We acknowledge the Human Genome Center at the Institute of Medical Sciences of Tokyo University for use of its databases. Finally, we thank A. Nose and J. Thomas very much for critical comments about our manuscript. This work was supported by a Grant-in-Aid for Creative Fundamental Research from the Ministry of Education, Science, and Culture of Japan to M. T.; T. U. is a recipient of a Fellowship of the Japan Society for the Promotion of Science for Junior Scientists.
PY - 1997/7
Y1 - 1997/7
N2 - We identified DN-cadherin, a novel Drosophila cadherin that is expressed in axons and in the mesoderm. Although DN-cadherin has diverged from vertebrate classic cadherins in terms of its extracellular structure, it still can form a complex with catenins and induce cell aggregation, as do the vertebrate molecules. Loss-of-function mutations of the gene resulted in either embryonic lethality or uncoordinated locomotion of adults. In the central nervous system of null mutant embryos, subsets of ipsilateral axons displayed a variety of aberrant trajectories including failure of position shifts, defective bundling, and errors in directional migration of growth cones. These results suggest that processes of axon patterning critically depend on DN-cadherin-mediated axon-axon interactions.
AB - We identified DN-cadherin, a novel Drosophila cadherin that is expressed in axons and in the mesoderm. Although DN-cadherin has diverged from vertebrate classic cadherins in terms of its extracellular structure, it still can form a complex with catenins and induce cell aggregation, as do the vertebrate molecules. Loss-of-function mutations of the gene resulted in either embryonic lethality or uncoordinated locomotion of adults. In the central nervous system of null mutant embryos, subsets of ipsilateral axons displayed a variety of aberrant trajectories including failure of position shifts, defective bundling, and errors in directional migration of growth cones. These results suggest that processes of axon patterning critically depend on DN-cadherin-mediated axon-axon interactions.
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U2 - 10.1016/S0896-6273(00)80349-9
DO - 10.1016/S0896-6273(00)80349-9
M3 - Article
C2 - 9247265
AN - SCOPUS:0030861051
SN - 0896-6273
VL - 19
SP - 77
EP - 89
JO - Neuron
JF - Neuron
IS - 1
ER -