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Expression and function of Caenorhabditis elegans UNCP-18, a paralog of the SM protein UNC-18
被引:0
|作者:
Boeglin, Marion
[1
,2
]
Leyva-Diaz, Eduardo
[1
,3
]
Hobert, Oliver
[1
,4
]
机构:
[1] Columbia Univ, Howard Hughes Med Inst, Dept Biol Sci, New York, NY 10027 USA
[2] Univ Strasbourg, Dept Dev & Stem Cells, INSERM U1258, IGBMC,CNRS,UMR 7104, F-67081 Strasbourg, France
[3] Inst Neurosciencias, CSIC UMH, Sant Joan dAlacant 03550, Spain
[4] Columbia Univ, 1212 Amsterdam Ave, New York, NY 10027 USA
来源:
关键词:
C;
elegans;
SM protein;
secretory pathway;
nervous system;
behavior;
SYNAPTIC-TRANSMISSION;
GENE ENCODES;
SECRETION;
SENSITIVITY;
SYNTAXIN;
SNARE;
MICE;
D O I:
10.1093/genetics/iyad180
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Sec1/Munc18 (SM) proteins are important regulators of SNARE complex assembly during exocytosis throughout all major animal tissue types. However, expression of a founding member of the SM family, UNC-18, is mostly restricted to the nervous system of the nematode Caenorhabditis elegans, where it is important for synaptic transmission. Moreover, unc-18 null mutants do not display the lethality phenotype associated with (a) loss of all Drosophila and mouse orthologs of unc-18 and (b) with complete elimination of synaptic transmission in C. elegans. We investigated whether a previously uncharacterized unc-18 paralog, which we named uncp-18, may be able to explain the restricted expression and limited phenotypes of unc-18 null mutants. A reporter allele shows ubiquitous expression of uncp-18. Analysis of uncp-18 null mutants, unc-18 and uncp-18 double null mutants, as well as overexpression of uncp-18 in an unc-18 null mutant background, shows that these 2 genes can functionally compensate for one another and are redundantly required for embryonic viability. Our results indicate that the synaptic transmission defects of unc-18 null mutants cannot necessarily be interpreted as constituting a null phenotype for SM protein function at the synapse.
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