Lundquist E A, Herman R K
Department of Genetics and Cell Biology, University of Minnesota, St. Paul 55108.
Genetics. 1994 Sep;138(1):83-101. doi: 10.1093/genetics/138.1.83.
Mutations in the Caenorhabditis elegans gene mec-8 were previously shown to cause defects in mechanosensation and in the structure and dye filling of certain chemosensory neurons. Using noncomplementation screens, we have identified eight new mec-8 alleles and a deficiency that uncovers the locus. Strong mec-8 mutants exhibit an incompletely penetrant cold-sensitive embryonic and larval arrest, which we have correlated with defects in the attachment of body muscle to the hypodermis and cuticle. Mutations in mec-8 strongly enhance the mutant phenotype of unc-52(viable) mutations; double mutants exhibit an unconditional arrest and paralysis at the twofold stage of embryonic elongation, a phenotype characteristic of lethal alleles of unc-52, a gene previously shown to encode a homolog of the core protein of heparan sulfate proteoglycan, found in basement membrane, and to be involved in the anchorage of myofilament lattice to the muscle cell membrane. We have identified and characterized four extragenic recessive suppressors of a mec-8; unc-52(viable) synthetic lethality. The suppressors, which define the genes smu-1 and smu-2, can weakly suppress all mec-8 mutant phenes. They also suppress the muscular dystrophy conferred by an unc-52(viable) mutation.
秀丽隐杆线虫基因mec-8的突变先前已被证明会导致机械感觉以及某些化学感觉神经元的结构和染料填充出现缺陷。通过非互补筛选,我们鉴定出了八个新的mec-8等位基因和一个揭示该基因座的缺失。强mec-8突变体表现出不完全显性的冷敏感胚胎和幼虫停滞,我们已将其与体壁肌肉附着于皮下组织和角质层的缺陷相关联。mec-8中的突变强烈增强了unc-52(可存活)突变的突变表型;双突变体在胚胎伸长的两倍阶段表现出无条件停滞和麻痹,这是unc-52致死等位基因的特征性表型,unc-52基因先前已被证明编码硫酸乙酰肝素蛋白聚糖核心蛋白的同源物,存在于基底膜中,并参与肌丝晶格与肌肉细胞膜的锚定。我们已经鉴定并表征了mec-8;unc-52(可存活)合成致死性的四个基因外隐性抑制子。这些抑制子定义了s mu-1和s mu-2基因,它们可以微弱地抑制所有mec-8突变表型。它们还抑制由unc-52(可存活)突变导致的肌肉营养不良。