Rushforth A M, White C C, Anderson P
Department of Genetics, University of Wisconsin, Madison, Wisconsin 53706, USA.
Genetics. 1998 Nov;150(3):1067-77. doi: 10.1093/genetics/150.3.1067.
Caenorhabditis elegans contains two muscle regulatory myosin light chain genes, mlc-1 and mlc-2. To determine their in vivo roles, we identified deletions that eliminate each gene individually and both genes in combination. Functions of mlc-1 are redundant to those of mlc-2 in both body-wall and pharyngeal muscle. mlc-1(0) mutants are wild type, but mlc-1(0) mlc-2(0) double mutants arrest as incompletely elongated L1 larvae, having both pharyngeal and body-wall muscle defects. Transgenic copies of either mlc-1(+) or mlc-2(+) rescue all defects of mlc-1(0) mlc-2(0) double mutants. mlc-2 is redundant to mlc-1 in body-wall muscle, but mlc-2 performs a nearly essential role in the pharynx. Approximately 90% of mlc-2(0) hermaphrodites arrest as L1 larvae due to pharyngeal muscle defects. Lethality of mlc-2(0) mutants is sex specific, with mlc-2(0) males being essentially wild type. Four observations suggest that hermaphrodite-specific lethality of mlc-2(0) mutants results from insufficient expression of the X-linked mlc-1(+) gene in the pharynx. First, mlc-1(0) mlc-2(0) double mutants are fully penetrant L1 lethals in both hermaphrodites and males. Second, in situ localization of mlc mRNAs demonstrates that both mlc-1 and mlc-2 are expressed in the pharynx. Third, transgenic copies of either mlc-1(+) or mlc-2(+) rescue the pharyngeal defects of mlc-1(0) mlc-2(0) hermaphrodites. Fourth, a mutation of the dosage compensation gene sdc-3 suppresses hermaphrodite-specific lethality of mlc-2(0) mutants.
秀丽隐杆线虫含有两个肌肉调节性肌球蛋白轻链基因,mlc - 1和mlc - 2。为了确定它们在体内的作用,我们鉴定了分别消除每个基因以及同时消除这两个基因的缺失突变体。mlc - 1在体壁肌和咽肌中的功能与mlc - 2的功能冗余。mlc - 1(0)突变体是野生型,但mlc - 1(0)mlc - 2(0)双突变体停滞为未完全伸长的L1幼虫,同时具有咽肌和体壁肌缺陷。mlc - 1(+)或mlc - 2(+)的转基因拷贝可挽救mlc - 1(0)mlc - 2(0)双突变体的所有缺陷。mlc - 2在体壁肌中与mlc - 1功能冗余,但mlc - 2在咽中发挥着几乎必不可少的作用。约90%的mlc - 2(0)雌雄同体由于咽肌缺陷而停滞为L1幼虫。mlc - 2(0)突变体的致死性具有性别特异性,mlc - 2(0)雄性基本为野生型。四项观察结果表明,mlc - 2(0)突变体雌雄同体特异性致死是由于咽中X连锁的mlc - 1(+)基因表达不足所致。第一,mlc - 1(0)mlc - 2(0)双突变体在雌雄同体和雄性中都是完全致死的L1幼虫。第二,mlc mRNA的原位定位表明mlc - 1和mlc - 2在咽中均有表达。第三,mlc - 1(+)或mlc - 2(+)的转基因拷贝可挽救mlc - 1(0)mlc - 2(0)雌雄同体的咽缺陷。第四,剂量补偿基因sdc - 3的突变可抑制mlc - 2(0)突变体雌雄同体特异性致死。