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LPA19是拟南芥中Psb27的同源物,在光系统II生物发生过程中促进D1蛋白前体的加工。

LPA19, a Psb27 homolog in Arabidopsis thaliana, facilitates D1 protein precursor processing during PSII biogenesis.

作者信息

Wei Lili, Guo Jinkui, Ouyang Min, Sun Xuwu, Ma Jinfang, Chi Wei, Lu Congming, Zhang Lixin

机构信息

Fr Photosynthesis Research Center, Key Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.

出版信息

J Biol Chem. 2010 Jul 9;285(28):21391-8. doi: 10.1074/jbc.M110.105064. Epub 2010 May 5.

Abstract

The biogenesis and assembly of photosystem II (PSII) are mainly regulated by the nuclear-encoded factors. To further identify the novel components involved in PSII biogenesis, we isolated and characterized a high chlorophyll fluorescence low psii accumulation19 (lpa19) mutant, which is defective in PSII biogenesis. LPA19 encodes a Psb27 homolog (At1g05385). Interestingly, another Psb27 homolog (At1g03600) in Arabidopsis was revealed to be required for the efficient repair of photodamaged PSII. These results suggest that the Psb27 homologs play distinct functions in PSII biogenesis and repair in Arabidopsis. Chloroplast protein labeling assays showed that the C-terminal processing of D1 in the lpa19 mutant was impaired. Protein overlay assays provided evidence that LPA19 interacts with D1, and coimmunoprecipitation analysis demonstrated that LPA19 interacts with mature D1 (mD1) and precursor D1 (pD1). Moreover, LPA19 protein was shown to specifically interact with the soluble C terminus present in the precursor and mature D1 through yeast two-hybrid analyses. Thus, these studies suggest that LPA19 is involved in facilitating the D1 precursor protein processing in Arabidopsis.

摘要

光系统II(PSII)的生物发生和组装主要受核编码因子调控。为了进一步鉴定参与PSII生物发生的新组分,我们分离并鉴定了一个高叶绿素荧光低PSII积累19(lpa19)突变体,该突变体在PSII生物发生方面存在缺陷。LPA19编码一个Psb27同源物(At1g05385)。有趣的是,拟南芥中的另一个Psb27同源物(At1g03600)被发现是光损伤PSII有效修复所必需的。这些结果表明,Psb27同源物在拟南芥的PSII生物发生和修复中发挥着不同的功能。叶绿体蛋白标记试验表明,lpa19突变体中D1的C末端加工受损。蛋白质印迹试验提供了LPA19与D1相互作用的确凿证据,免疫共沉淀分析表明LPA19与成熟D1(mD1)和前体D1(pD1)相互作用。此外,通过酵母双杂交分析表明,LPA19蛋白与前体和成熟D1中存在的可溶性C末端特异性相互作用。因此,这些研究表明LPA19参与促进拟南芥中D1前体蛋白的加工。

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