Functional properties of the unc-64 gene encoding a Caenorhabditis elegans syntaxin

被引:72
作者
Ogawa, H
Harada, S
Sassa, T
Yamamoto, H
Hosono, R
机构
[1] Kanazawa Univ, Fac Med, Dept Phys Informat, Kanazawa, Ishikawa 920, Japan
[2] Kanazawa Univ, Fac Med, Dept Biochem, Kanazawa, Ishikawa 920, Japan
[3] Univ Tokushima, Sch Med, Dept Nutr, Tokushima 770, Japan
[4] Fujita Hlth Univ, Dept Biol, Aichi 47011, Japan
关键词
D O I
10.1074/jbc.273.4.2192
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
Phenotypes of Caenorhabditis elegans unc-18 and unc-64 gene mutations are similar. While unc-18 is known to be essential for normal synaptic transmission (Hosono, R., Hekimi, S., Kamiya, Y., Sassa, T., Murakami, S., Nishiwaki, S., Miwa, J., Taketo, A, and Kodaira, K.-I. (1992) J. Neurochem. 58, 1517-1525), the function of unc-64 remains unclear. Here we describe the cloning, and the molecular and genetic characterization of the unc-64 gene, especially in relation to unc-18. unc-64 encodes a protein (C. elegans syntaxin) showing sequence and structural similarities to mammalian syntaxin 1A. From unc-64, at least three types of poly(A)(+) RNA are transcribed, which encode two types of syntaxin that differ in the deduced transmembrane domain. In gene expression, unc-64 closely resembles unc-18, that is, both are expressed in neural cells, especially in motor neurons and neurons constituting head ganglions. C. elegans syntaxin binds to UNC-18 with high affinity. The unc-64 (e246) mutation producing a mild phenotype causes an Ala --> Val conversion in the conserved COOH-terminal region in mammalian syntaxin 1A or Drosophila syntaxin-1A whose site is included in three types of transcripts. The binding of the mutant C. elegans syntaxin tb UNC-18 is greatly reduced, indicating the mutation Site contributes to the binding.
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页码:2192 / 2198
页数:7
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