Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, NewYork, NY 10027, USA.
Department of Development and Stem Cells, IGBMC, CNRS UMR 7104/INSERM U1258, Université de Strasbourg, Strasbourg 67081, France.
Genetics. 2023 Dec 6;225(4). doi: 10.1093/genetics/iyad180.
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.
Sec1/Munc18(SM)蛋白是所有主要动物组织类型中胞吐作用过程中 SNARE 复合物组装的重要调节剂。然而,SM 家族的一个创始成员 UNC-18 的表达主要局限于线虫秀丽隐杆线虫的神经系统,在那里它对突触传递很重要。此外,unc-18 缺失突变体不会表现出与(a)丧失所有果蝇和小鼠 UNC-18 同源物以及(b)线虫中完全消除突触传递相关的致死表型。我们研究了一个以前未表征的 unc-18 旁系同源物(我们称之为 uncp-18)是否能够解释 unc-18 缺失突变体的限制表达和有限表型。报告基因等位基因显示 uncp-18 的广泛表达。对 unc-18 缺失突变体、unc-18 和 uncp-18 双缺失突变体以及 uncp-18 在 unc-18 缺失突变体背景下的过表达进行分析表明,这 2 个基因可以在功能上相互补偿,并且冗余地需要胚胎活力。我们的结果表明,unc-18 缺失突变体的突触传递缺陷不一定可以解释为突触处 SM 蛋白功能的缺失表型。