FEBS Letters | |
Distinct roles of the Src family kinases, SRC‐1 and KIN‐22, that are negatively regulated by CSK‐1 in C. elegans | |
Okada, Masato1  Hirose, Takashi1  Ohshima, Yasumi2  Koga, Makoto2  | |
[1] Department of Oncogene Research, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan;Department of Biology, Faculty of Sciences, Kyushu University Graduate School, Fukuoka 812-8581, Japan | |
关键词: csk-1; src-1; kin-22; Tyrosine kinase; Caenorhabditis elegans; SFK; Src family kinase; PTK; protein tyrosine kinase; Csk; C-terminal Src kinase; SH2; Src homology 2; SH3; Src homology 3; SMART; simple module architecture research tool; DIC; differential interference contrast; | |
DOI : 10.1016/S0014-5793(02)03819-X | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
To elucidate the primitive roles of the Src family kinases (SFKs), here we characterized Caenorhabditis elegans orthologues of SFKs (src-1 and kin-22) and their regulator kinase Csk (csk-1). SRC-1 and KIN-22 possess the C-terminal regulatory tyrosines characteristic of SFKs, and their activities are negatively regulated by CSK-1 in a yeast expression system. The src-1 and csk-1 genes are co-expressed in some head neurons, the anchor cell and the tail region, while kin-22 and csk-1 genes are co-expressed in pharyngeal muscles and tail region. Expression of KIN-22 induced morphological defects in the pharynx, whereas expression of SRC-1 did not show any overt phenotype in adult. RNA interference of src-1, but not that of kin-22, caused a developmental arrest in early development. These results suggest that SRC-1 and KIN-22 play distinct roles under the control of CSK-1.
【 授权许可】
Unknown
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