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首页> 外文期刊>Journal of phycology >PHOTOSYNTHETIC ELECTRON TRANSPORT MEDIATES THE LIGHT-CONTROLLED UP-REGULATION OF EXPRESSION OF METHIONINE SULFOXIDE REDUCTASE A AND B FROM MARINE MACROALGA ULVA FASCIATA
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PHOTOSYNTHETIC ELECTRON TRANSPORT MEDIATES THE LIGHT-CONTROLLED UP-REGULATION OF EXPRESSION OF METHIONINE SULFOXIDE REDUCTASE A AND B FROM MARINE MACROALGA ULVA FASCIATA

机译:光合作用的电子传输介导了海洋巨藻中甲硫氨酸还原酶A和B的表达受光控制的上调

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摘要

Methionine (Met) residues of proteins can be oxidized by reactive oxygen species (ROS) with the formation of two epimers of methionine sulfoxide, S-MetSO and R-MetSO, which are reduced back to methionine by methionine sulfoxide reductase A (MSRA) and B (MSRB), respectively. UfMSRA and UfMSRB were cloned from the marine macroalga Ulva fasciata Delile, and the role of retrograde signal in gene expression was studied. Transcripts of UfMSRA and UfMSRB were increased after light exposure with a peak at 1 h. Treatment of photosynthetic electron transport inhibitors, 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (DBMIB), or stigmatellin, promoted the light-activated increase in UfMSRA transcripts, and a PSI electron donor, 2,6-dichlorophenolindophenol (DCPIP), reversed their effects. Increase of UfMSRB transcript by light was inhibited by DCMU and DBMIB treatments, and their effects were not reversed by DCPIP. Stigmatellin treatment did not affect UfMSRB transcripts. Thus, a relatively oxidized state of electron transport downstream from the cytochrome b(6)f (cytb(6)f ) complex is involved in the light up-regulation of UfMSRA gene expression, and a more reduced state of Q(o) of the cytb(6)f complex is required for the light activation of gene expression of UfMSRB.
机译:蛋白质的蛋氨酸(Met)残基可以被活性氧(ROS)氧化,形成蛋氨酸亚砜的两个差向异构体S-MetSO和R-MetSO,它们被蛋氨酸亚砜还原酶A(MSRA)和甲硫氨酸还原成蛋氨酸。 B(MSRB)分别。从海洋大型藻类Ulva fasciata Delile克隆了UfMSRA和UfMSRB,并研究了逆行信号在基因表达中的作用。曝光后UfMSRA和UfMSRB的转录本增加,在1 h达到峰值。光合作用电子传输抑制剂,3-(3,4-二氯苯基)-1,1-二甲基脲(DCMU),2,5-二溴-3-甲基-6-异丙基-对苯醌(DBMIB)或柱头蛋白的治疗促进了UfMSRA转录物的光激活增加,PSI电子供体2,6-二氯苯酚吲哚酚(DCPIP)逆转了其作用。 DCMU和DBMIB处理抑制了光引起的UfMSRB转录物的增加,而DCPIP并没有逆转它们的作用。柱头蛋白治疗不影响UfMSRB转录本。因此,从细胞色素b(6)f(cytb(6)f)复合物向下游的电子传输的相对氧化态参与UfMSRA基因表达的光上调,而Q(o)的降低态cytb(6)f复合物是UfMSRB基因表达的光激活所必需的。

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