Aroian R V, Sternberg P W
Howard Hughes Medical Institute, Division of Biology, California Institute of Technology, Pasadena 91125.
Genetics. 1991 Jun;128(2):251-67. doi: 10.1093/genetics/128.2.251.
The let-23 gene, which encodes a putative tyrosine kinase of the epidermal growth factor (EGF) receptor subfamily, has multiple functions during Caenorhabditis elegans development. We show that let-23 function is required for vulval precursor cells (VPCs) to respond to the signal that induces vulval differentiation: a complete loss of let-23 function results in no induction. However, some let-23 mutations that genetically reduce but do not eliminate let-23 function result in VPCs apparently hypersensitive to inductive signal: as many as five of six VPCs can adopt vulval fates, in contrast to the three that normally do. These results suggest that the let-23 receptor tyrosine kinase controls two opposing pathways, one that stimulates vulval differentiation and another that negatively regulates vulval differentiation. Furthermore, analysis of 16 new let-23 mutations indicates that the let-23 kinase functions in at least five tissues. Since various let-23 mutant phenotypes can be obtained independently, the let-23 gene is likely to have tissue-specific functions.
let-23基因编码表皮生长因子(EGF)受体亚家族的一种假定酪氨酸激酶,在秀丽隐杆线虫发育过程中具有多种功能。我们发现,外阴前体细胞(VPC)对诱导外阴分化的信号作出反应需要let-23发挥功能:let-23功能完全丧失会导致无法诱导分化。然而,一些在遗传学上降低但未消除let-23功能的突变会导致VPC对诱导信号明显超敏:多达六分之五的VPC可采用外阴命运,而正常情况下只有三个VPC会如此。这些结果表明,let-23受体酪氨酸激酶控制着两条相反的途径,一条刺激外阴分化,另一条对外阴分化起负调节作用。此外,对16个新的let-23突变的分析表明,let-23激酶在至少五个组织中发挥作用。由于各种let-23突变表型可独立获得,因此let-23基因可能具有组织特异性功能。