首页> 美国卫生研究院文献>Plant Physiology >Separate photosensory pathways co-regulate blue light/ultraviolet-A-activated psbD-psbC transcription and light-induced D2 and CP43 degradation in barley (Hordeum vulgare) chloroplasts.
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Separate photosensory pathways co-regulate blue light/ultraviolet-A-activated psbD-psbC transcription and light-induced D2 and CP43 degradation in barley (Hordeum vulgare) chloroplasts.

机译:大麦(大麦)叶绿体中单独的光敏途径共同调节蓝光/紫外线-A激活的psbD-psbC转录以及光诱导的D2和CP43降解。

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摘要

We studied the effects of spectral quality and fluence on the expression of several chloroplast-encoded photosynthesis genes and on the stability of their protein products in barley (Hordeum vulgare). During light-dependent chloroplast maturation, mRNA levels for psbD-psbC and psbA were maintained at higher levels compared with mRNAs encoding proteins for other photosynthesis functions (atpB, rbcL). Maintenance of psbD-psbC mRNA levels was accounted for by differential activation of the psbD-psbC light-responsive promoter by high-irradiance blue light and, secondarily, ultraviolet A (UV-A) radiation. Promoter activation was fluence dependent and required continuous illumination for 2 h at threshold fluences of 1.3 (blue light), 7.5 (white light), or 10 (UV-A) mumol m-2 s-1. From immunoblot analysis experiments, we showed that the psbD-psbC gene products D2 and CP43 undergo light-mediated turnover similar to light-labile D1. Other photosynthesis proteins such as the beta subunit of ATP synthase and the large subunit of ribulose-1,5-bisphosphate carboxylase were relatively stable. In the absence of protein synthesis, D2 degradation paralleled the degradation of D1 (relative half-lives, 9.5-10 h). CP43 decay was about half of D2 and D1 decay. In contrast with activation of the light-responsive promoter, the fluence-dependent degradation of D1, D2, and CP43 required 50- to 100-fold higher fluences of photosynthetically active white, red, blue, or UV-A irradiation. We interpret the different fluence and wavelength requirements to indicate that separate photosensory systems regulate activation of psbD-psbC transcription and turnover of D1, D2, and CP43. We propose that a blue light/UV-A photosensory pathway activates the psbD-psbC light-responsive promoter, differentially maintaining the capacity of mature chloroplasts to synthesize D2 and CP43, which are damaged and turned over in illuminated plants.
机译:我们研究了光谱质量和能量密度对大麦(Hordeum vulgare)中几个叶绿体编码的光合作用基因的表达及其蛋白产物稳定性的影响。在光依赖性叶绿体成熟过程中,与编码其他光合作用蛋白(atpB,rbcL)的mRNA相比,psbD-psbC和psbA的mRNA水平维持在较高水平。维持psbD-psbC mRNA水平的原因是通过高辐射蓝光和其次是紫外线A(UV-A)辐射对psbD-psbC光响应性启动子的差异激活。启动子的激活取决于注量,需要以1.3(蓝光),7.5(白光)或10(UV-A)mumol m-2 s-1的阈值注量连续照明2 h。从免疫印迹分析实验中,我们显示psbD-psbC基因产物D2和CP43经历类似于光不稳定D1的光介导的周转。其他光合作用蛋白,例如ATP合酶的β亚基和1,5-双磷酸核糖羧化酶的大亚基,相对稳定。在没有蛋白质合成的情况下,D2降解与D1降解平行(相对半衰期9.5-10小时)。 CP43衰减约为D2和D1衰减的一半。与光响应性启动子的激活相反,D1,D2和CP43的依赖注量的降解需要光合作用的白色,红色,蓝色或UV-A辐射的注量要高50至100倍。我们解释了不同的注量和波长要求,以表明单独的光敏系统调节psbD-psbC转录的激活以及D1,D2和CP43的更新。我们建议,蓝光/ UV-A光感测途径激活psbD-psbC光响应性启动子,差异地维持成熟叶绿体合成D2和CP43的能力,D2和CP43在被照亮的植物中受损并被移交。

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