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对 photosystem II 除草剂敌草隆的抗性在蓝藻 Synechococcus sp. PCC7942 中是显性的,对其敏感性是隐性的。

Resistance to the photosystem II herbicide diuron is dominant to sensitivity in the cyanobacterium Synechococcus sp. PCC7942.

机构信息

Department of Molecular Genetics and Cell Biology. The University of Chicago, Chicago, IL 60637, USA.

出版信息

EMBO J. 1989 Apr;8(4):1237-45. doi: 10.1002/j.1460-2075.1989.tb03497.x.

DOI:10.1002/j.1460-2075.1989.tb03497.x
PMID:16453875
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC400940/
Abstract

The transformable cyanobacterium, Synechococcus sp. PCC7942, was used to study the genetics of resistance to the herbicide diuron. In wild-type cells, diuron binds to one of the core proteins, called D1, of photosystem II reaction centres. This binding prevents the transfer of electrons from Q(A), the primary quinone acceptor, to Q(B), which is necessary to create the charge separation that drives ATP synthesis. A single amino acid substitution in the D1 protein reduces diuron binding and confers herbicide resistance to reaction centres containing the substituted D1 protein. In Synechococcus 7942, the D1 protein is encoded by three functional genes called psbAI, psbAII and psbAIII. By selectively altering one member at a time of the three-member psbA gene family, we have demonstrated that diuron-resistant alleles are dominant to diuron-sensitive alleles. The relative abundance of the different psbA gene transcripts is correlated with the fraction of diuron-resistant reaction centres and with the degree of diuron resistance. Growth in sublethal diuron selectively increases the steady-state levels of transcripts of genes (psbA and psbD) encoding the core proteins of photosystem II. We have also found that turnover of the D1 protein can be uncoupled from electron transport through photosystem II.

摘要

可转化蓝藻,集胞藻 PCC7942,被用于研究对除草剂敌草隆的抗性的遗传学。在野生型细胞中,敌草隆与光合作用 II 反应中心的核心蛋白之一 D1 结合。这种结合阻止电子从 Q(A),主要的醌受体,转移到 Q(B),这是驱动 ATP 合成所必需的。D1 蛋白中的单个氨基酸取代会降低敌草隆的结合,并赋予含有取代 D1 蛋白的反应中心对除草剂的抗性。在集胞藻 7942 中,D1 蛋白由三个功能基因 psbAI、psbAII 和 psbAIII 编码。通过选择性地一次改变三成员 psbA 基因家族中的一个成员,我们已经证明敌草隆抗性等位基因是对敌草隆敏感等位基因的显性。不同 psbA 基因转录本的相对丰度与敌草隆抗性反应中心的分数和敌草隆抗性的程度相关。亚致死剂量的敌草隆选择性地增加了编码光合作用 II 核心蛋白的基因(psbA 和 psbD)的转录本的稳态水平。我们还发现,D1 蛋白的周转可以与通过光合作用 II 的电子传递解偶联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/8d658df7bdff/emboj00128-0241-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/84e39a50967b/emboj00128-0238-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/ec9978c5af5a/emboj00128-0239-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/8d658df7bdff/emboj00128-0241-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/84e39a50967b/emboj00128-0238-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/ec9978c5af5a/emboj00128-0239-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff8/400940/8d658df7bdff/emboj00128-0241-a.jpg

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本文引用的文献

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Form II of D1 is important during transition from standard to high light intensity in Synechococcus sp. strain PCC 7942.D1 型蛋白的 II 形式在聚球藻 PCC 7942 从标准光照强度向高光强过渡过程中非常重要。
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nblS, a gene involved in controlling photosynthesis-related gene expression during high light and nutrient stress in Synechococcus elongatus PCC 7942.nblS,一个参与调控聚球藻7942在高光和营养胁迫期间光合作用相关基因表达的基因。
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Functional analysis of the two homologous psbA gene copies in Synechocystis PCC 6714 and PCC 6803.集胞藻PCC 6714和PCC 6803中两个同源psbA基因拷贝的功能分析。
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Adaptation to high light intensity in Synechococcus sp. strain PCC 7942: regulation of three psbA genes and two forms of the D1 protein.聚球藻属PCC 7942菌株对高光强度的适应:三个psbA基因和两种形式的D1蛋白的调控
J Bacteriol. 1994 Feb;176(4):959-65. doi: 10.1128/jb.176.4.959-965.1994.
9
Differential expression of members of a cyanobacterial psbA gene family in response to light.蓝藻psbA基因家族成员对光响应的差异表达
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10
Characterization of a four-member psbA gene family from the cyanobacterium Anabaena PCC 7120.来自鱼腥藻Anabaena PCC 7120的一个由四个成员组成的psbA基因家族的特征分析
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Relocating a gene for herbicide tolerance: A chloroplast gene is converted into a nuclear gene.将抗除草剂基因转移:将叶绿体基因转化为核基因。
Proc Natl Acad Sci U S A. 1988 Jan;85(2):391-5. doi: 10.1073/pnas.85.2.391.
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Membrane protein damage and repair: Selective loss of a quinone-protein function in chloroplast membranes.膜蛋白损伤与修复:叶绿体膜中醌蛋白功能的选择性丧失。
Proc Natl Acad Sci U S A. 1984 Jul;81(13):4070-4. doi: 10.1073/pnas.81.13.4070.
7
Regulation of protein metabolism: Coupling of photosynthetic electron transport to in vivo degradation of the rapidly metabolized 32-kilodalton protein of the chloroplast membranes.蛋白质代谢的调节:光合作用电子传递与叶绿体膜中快速代谢的 32kDa 蛋白体内降解的偶联。
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Lithium dodecyl sulfate/polyacrylamide gel electrophoresis of thylakoid membranes at 4 degrees C: Characterizations of two additional chlorophyll a-protein complexes.4℃下类囊体膜的十二烷基硫酸锂/聚丙烯酰胺凝胶电泳:另外两种叶绿素a-蛋白复合物的特性分析
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Light-dependent degradation of the Q(B)-protein in isolated pea thylakoids.光依赖性的质体醌(Q(B)-蛋白)在分离的豌豆类囊体中的降解。
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Optimal conditions for genetic transformation of the cyanobacterium Anacystis nidulans R2.蓝藻念珠藻Anacystis nidulans R2遗传转化的最佳条件
J Bacteriol. 1984 Apr;158(1):36-42. doi: 10.1128/jb.158.1.36-42.1984.