Morgan W R, Greenwald I
Department of Molecular Biology, Princeton University, New Jersey 08544.
Mol Cell Biol. 1993 Nov;13(11):7133-43. doi: 10.1128/mcb.13.11.7133-7143.1993.
We describe our characterization of kin-15 and kin-16, a tandem pair of homologous Caenorhabditis elegans genes encoding transmembrane protein tyrosine kinases (PTKs) with an unusual structure: the predicted extracellular domain of each putative gene product is only about 50 amino acids, and there are no potential autophosphorylation sites in the C-terminal domain. Using lacZ fusions, we found that kin-15 and kin-16 both appear to be expressed during postembryonic development in the large hypodermal syncytium (hyp7) around the time that specific hypodermal cells fuse with hyp7. kin-15 and kin-16 were positioned on the genetic and physical maps, but extrachromosomal arrays containing wild-type kin-15 and/or kin-16 genes were unable to complement candidate lethal mutations. The results suggest that kin-15 and kin-16 may be specifically involved in cell-cell interactions regulating cell fusions that generate the hypodermis during postembryonic development.
我们描述了对kin-15和kin-16的特性研究,它们是秀丽隐杆线虫中的一对同源基因,编码具有独特结构的跨膜蛋白酪氨酸激酶(PTK):每个推测的基因产物的预测细胞外结构域仅约50个氨基酸,并且在C末端结构域中没有潜在的自磷酸化位点。使用lacZ融合,我们发现kin-15和kin-16似乎都在胚胎后发育期间,在特定的皮下细胞与hyp7融合时,在大的皮下合胞体(hyp7)中表达。kin-15和kin-16定位在遗传图谱和物理图谱上,但含有野生型kin-15和/或kin-16基因的染色体外阵列无法互补候选致死突变。结果表明,kin-15和kin-16可能特别参与调节胚胎后发育过程中产生皮下组织的细胞融合的细胞间相互作用。