Shreffler W, Magardino T, Shekdar K, Wolinsky E
Department of Biochemistry, New York University Medical School, New York 10016, USA.
Genetics. 1995 Mar;139(3):1261-72. doi: 10.1093/genetics/139.3.1261.
Two Caenorhabditis elegans genes, unc-8 and sup-40, have been newly identified, by genetic criteria, as regulating ion channel function in motorneurons. Two dominant unc-8 alleles cause motorneuron swelling similar to that of other neuronal types in dominant mutants of the deg-1 gene family, which is homologous to a mammalian gene family encoding amiloride-sensitive sodium channel subunits. As for previously identified deg-1 family members, unc-8 dominant mutations are recessively suppressed by mutations in the mec-6 gene, which probably encodes a second type of channel component. An unusual dominant mutation, sup-41 (lb125), also co-suppresses unc-8 and deg-1, suggesting the existence of yet another common component of ion channels containing unc-8 or deg-1 subunits. Dominant, transacting, intragenic suppressor mutations have been isolated for both unc-8 and deg-1, consistent with the idea that, like their mammalian homologues, the two gene products function as multimers. The sup-40 (lb130) mutation dominantly suppresses unc-8 motorneuron swelling and produces a novel swelling phenotype in hypodermal nuclei. sup-40 may encode an ion channel component or regulator that can correct the osmotic defect caused by abnormal unc-8 channels.
通过遗传学标准新鉴定出两种秀丽隐杆线虫基因unc-8和sup-40,它们在运动神经元中调节离子通道功能。两个显性unc-8等位基因导致运动神经元肿胀,类似于deg-1基因家族显性突变体中其他神经元类型的肿胀,该家族与编码氨氯地平敏感钠通道亚基的哺乳动物基因家族同源。至于先前鉴定的deg-1家族成员,unc-8显性突变可被mec-6基因中的突变隐性抑制,mec-6基因可能编码另一种通道成分。一个不寻常的显性突变sup-41(lb125)也共同抑制unc-8和deg-1,这表明存在另一种含有unc-8或deg-1亚基的离子通道共同成分。已分离出unc-8和deg-1的显性、反式作用、基因内抑制突变,这与以下观点一致:即这两种基因产物与其哺乳动物同源物一样,以多聚体形式发挥作用。sup-40(lb130)突变显性抑制unc-8运动神经元肿胀,并在皮下核中产生一种新的肿胀表型。sup-40可能编码一种离子通道成分或调节剂,可纠正由异常unc-8通道引起的渗透缺陷。