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蛋白激酶和质体外丝氨酸/苏氨酸蛋白磷酸酶参与调节大麦质体转录和psbD蓝光响应启动子的信号通路。

Involvement of protein kinase and extraplastidic serine/threonine protein phosphatases in signaling pathways regulating plastid transcription and the psbD blue light-responsive promoter in barley.

作者信息

Christopher D A, Li X, Kim M, Mullet J E

机构信息

Department of Plant Molecular Physiology, College of Tropical Agriculture and Human Resources, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA.

出版信息

Plant Physiol. 1997 Apr;113(4):1273-82. doi: 10.1104/pp.113.4.1273.

Abstract

We investigated the signaling pathways that control changes in plastid transcription in response to development and light. Plastid gene expression was analyzed in dark-grown barley (Hordeum vulgare L.) seedlings treated in vivo with an inhibitor of protein phosphatases 1 and 2A, okadaic acid (OA), or an inhibitor of protein kinases (K252a), followed by exposure of the seedlings to either red, blue, or white light. OA prevented blue light from activating the plastid pshD blue-light-responsive promoter (BLRP) and prevented red and blue light from activating the expression of the plastid-encoded rbcl and psbA and the nuclear-encoded RbcS and Lhcb genes. OA reduced total plastid transcription activity in dark- and light-grown seedlings by 77 to 80%, indicating that OA prevented light-responsive transcription by reducing total plastid transcription. In contrast, K252a activated the accumulation of mRNAs arising from the BLRP. Blue light in combination with K252a increased psbD mRNA levels in an additive manner. The results indicate that protein phosphatases 1 and/or 2A, which reside external to the organelle, are required for proper function of plastid transcription and chloroplast development, whereas a protein kinase represses the BLRP in plants grown in the dark.

摘要

我们研究了响应发育和光照控制质体转录变化的信号通路。对黑暗中生长的大麦(Hordeum vulgare L.)幼苗进行体内处理,用蛋白磷酸酶1和2A的抑制剂冈田酸(OA)或蛋白激酶抑制剂(K252a)处理,然后将幼苗暴露于红光、蓝光或白光下,分析质体基因表达。OA阻止蓝光激活质体pshD蓝光响应启动子(BLRP),并阻止红光和蓝光激活质体编码的rbcl和psbA以及核编码的RbcS和Lhcb基因的表达。OA使黑暗和光照下生长的幼苗中总的质体转录活性降低77%至80%,表明OA通过降低总的质体转录来阻止光响应转录。相反,K252a激活了源自BLRP的mRNA的积累。蓝光与K252a联合以累加方式增加了psbD mRNA水平。结果表明,位于细胞器外部的蛋白磷酸酶1和/或2A是质体转录和叶绿体发育正常功能所必需的,而蛋白激酶在黑暗中生长的植物中抑制BLRP。

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