Opperman Karla, Moseley-Alldredge Melinda, Yochem John, Bell Leslie, Kanayinkal Tony, Chen Lihsia
Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55455.
Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota 55455 Developmental Biology Center, University of Minnesota, Minneapolis, Minnesota 55455.
Genetics. 2015 Feb;199(2):497-509. doi: 10.1534/genetics.114.169581. Epub 2014 Dec 8.
The L1CAM family of cell adhesion molecules is a conserved set of single-pass transmembrane proteins that play diverse roles required for proper nervous system development and function. Mutations in L1CAMs can cause the neurological L1 syndrome and are associated with autism and neuropsychiatric disorders. L1CAM expression in the mature nervous system suggests additional functions besides the well-characterized developmental roles. In this study, we demonstrate that the gene encoding the Caenorhabditis elegans L1CAM, sax-7, genetically interacts with gtl-2, as well as with unc-13 and rab-3, genes that function in neurotransmission. These sax-7 genetic interactions result in synthetic phenotypes that are consistent with abnormal synaptic function. Using an inducible sax-7 expression system and pharmacological reagents that interfere with cholinergic transmission, we uncovered a previously uncharacterized nondevelopmental role for sax-7 that impinges on synaptic function.
细胞粘附分子L1CAM家族是一组保守的单次跨膜蛋白,在神经系统的正常发育和功能中发挥着多种作用。L1CAM的突变可导致神经性L1综合征,并与自闭症和神经精神疾病相关。L1CAM在成熟神经系统中的表达表明,除了已充分表征的发育作用外,它还有其他功能。在本研究中,我们证明,编码秀丽隐杆线虫L1CAM的基因sax-7与gtl-2以及在神经传递中起作用的unc-13和rab-3基因发生遗传相互作用。这些sax-7遗传相互作用导致的合成表型与异常突触功能一致。利用诱导型sax-7表达系统和干扰胆碱能传递的药理学试剂,我们发现了sax-7以前未被表征的非发育作用,该作用影响突触功能。