Komatsu S, Li W, Konishi H, Yoshikawa M, Konishi T, Yang G
Department of Molecular Genetics, National Institute of Agrobiological Sciences, Tsukuba, Japan.
Biol Pharm Bull. 2001 Nov;24(11):1316-9. doi: 10.1248/bpb.24.1316.
The Ca2+-dependent protein kinases (CDPKs) and abscisic acid (ABA) are known to be involved in low-temperature stress response. The focus of this study was to characterize the 45 kDa protein kinase identified in the crude extract of rice (Oryza sativa L.) seedling roots in response to cold (5 degrees C) stress. The activity of the 45 kDa protein kinase decreased at low temperature as evident by an in-gel kinase assay using histone III-S as a substrate. Also, the Ca2+-dependent activity of this protein kinase was suppressed by cold in the membrane fractions of the root. A general protein kinase inhibitor and Ca2+ chelator inhibited the activity of the 45 kDa protein kinase, suggesting that it was a plant CDPK. The 45 kDa CDPK identified was found to be independent of photosynthetic tissues such as the leaf and leaf sheath of rice seedlings, supporting a direct sensing mechanism in the roots of rice seedlings to cold stress. The suppressed activity of the 45 kDa CDPK was reverted by supplementing with 5 microM ABA under cold stress. The 45 kDa CDPK activity was stronger in the cold-tolerant variety of the 4 types tested than it was in the cold-sensitive one. These results suggest the involvement of endogenous ABA in regulating the activity of the 45 kDa CDPK in response to cold stress.
已知钙依赖蛋白激酶(CDPKs)和脱落酸(ABA)参与低温胁迫响应。本研究的重点是对在水稻(Oryza sativa L.)幼苗根粗提物中鉴定出的45 kDa蛋白激酶进行表征,该激酶响应低温(5摄氏度)胁迫。通过使用组蛋白III-S作为底物的凝胶内激酶测定法可以明显看出,45 kDa蛋白激酶的活性在低温下降低。此外,该蛋白激酶的钙依赖活性在根的膜组分中受到低温抑制。一种通用的蛋白激酶抑制剂和钙螯合剂抑制了45 kDa蛋白激酶的活性,表明它是一种植物CDPK。已鉴定出的45 kDa CDPK与水稻幼苗的光合组织如叶片和叶鞘无关,这支持了水稻幼苗根部对低温胁迫的直接感知机制。在低温胁迫下补充5 microM ABA可恢复45 kDa CDPK被抑制的活性。在所测试的4个品种中,45 kDa CDPK活性在耐寒品种中比在冷敏感品种中更强。这些结果表明内源性ABA参与调节45 kDa CDPK响应低温胁迫的活性。