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两种新突变导致蓝藻 Synechococcus sp. PCC 7002 除草剂抗性的遗传分析。

Genetic analysis of two new mutations resulting in herbicide resistance in the cyanobacterium Synechcoccus sp. PCC 7002.

机构信息

Department of Molecular and Cell Biology, Penn State University, 16802, University Park, PA, USA.

出版信息

Photosynth Res. 1988 Apr;16(1-2):83-99. doi: 10.1007/BF00039487.

DOI:10.1007/BF00039487
PMID:24430993
Abstract

Two herbicide-resistant strains of the cyanobacterium Synechococcus sp. PCC 7002 are compared to the wild-type with respect to the DNA changes which result in herbicide resstance. The mutations have previously been mapped to a region of the cyanobacterial genome which encodes oneof three copies of psbA, the gene which encodes the 32 kDa Qb-binding protein also known as D1 (Buzby et al. 1987). The DNA sequence of the wild-type gene was first determined and used as a comparison to that of the mutant alleles. A point mutation at codon 211 in the psbA1 coding locus (TTC) to TCC) results in an amino acid change from phenylalanine to serine in the D1 protein. This mutation confers resistance to atrazine and diuron at seven times and at two times the minimal inhibitory concentration (MIC) for the wild-type, respectively. A mutation at codon 211 resulting in herbicide resistance has not previously been described in the literature. A second point mutation at codon 219 in the psbA1 coding locus (GTA to ATA) results in an amino acid change from valine to isoleucine in the D1 protein. This mutation confers resistance to diuron and atrazine at ten times and at two times the MIC for the wild-type, respectively. An identical codon change conferring similar herbicide resistance patterns has previously been described in Chlamydomonas reinhardtii. The atrazine-resistance phenotype in Synechococcus sp. PCC 7002 was shown to be dominant by plasmid segregation analysis.

摘要

两种对除草剂具有抗性的鱼腥蓝细菌(Synechococcus sp. PCC 7002)品系与野生型相比,在导致除草剂抗性的 DNA 变化方面有所不同。这些突变先前已被定位到蓝藻基因组的一个区域,该区域编码 psbA 的三个拷贝之一,psbA 基因编码 32kDa Qb 结合蛋白,也称为 D1(Buzby 等人,1987)。野生型基因的 DNA 序列首先被确定,并用作与突变等位基因的比较。在 psbA1 编码基因座(TTC)中的密码子 211 处发生点突变(TTC)到 TCC)导致 D1 蛋白中的苯丙氨酸突变为丝氨酸。这种突变使 D1 蛋白对莠去津和敌草隆的抗性分别提高了 7 倍和 2 倍,MIC 为野生型的最低抑制浓度。在文献中尚未描述过导致除草剂抗性的密码子 211 突变。在 psbA1 编码基因座的密码子 219 处发生的第二个点突变(GTA 到 ATA)导致 D1 蛋白中的缬氨酸突变为异亮氨酸。这种突变使 D1 蛋白对敌草隆和莠去津的抗性分别提高了 10 倍和 2 倍,MIC 为野生型的最低抑制浓度。在先前已经描述过的莱茵衣藻(Chlamydomonas reinhardtii)中,相同的密码子变化赋予了类似的除草剂抗性模式。通过质粒分离分析表明,鱼腥蓝细菌(Synechococcus sp. PCC 7002)中的莠去津抗性表型是显性的。

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Genetic analysis of two new mutations resulting in herbicide resistance in the cyanobacterium Synechcoccus sp. PCC 7002.两种新突变导致蓝藻 Synechococcus sp. PCC 7002 除草剂抗性的遗传分析。
Photosynth Res. 1988 Apr;16(1-2):83-99. doi: 10.1007/BF00039487.
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引用本文的文献

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2
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Photosynth Res. 1990 May;24(2):137-50. doi: 10.1007/BF00032594.
3
The cyanobacterium Synechococcus modulates Photosystem II function in response to excitation stress through D1 exchange.

本文引用的文献

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Inhibitors of photosystem II and the topology of the herbicide and QB binding polypeptide in the thylakoid membrane.光系统 II 抑制剂与类囊体膜中除草剂和 Qb 结合多肽的拓扑结构。
Photosynth Res. 1986 Jan;10(3):381-92. doi: 10.1007/BF00118304.
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Isolation, sequence and expression of two members of the 32 kd thylakoid membrane protein gene family from the cyanobacterium Anabaena 7120.从蓝藻鱼腥藻 7120 中分离、测序并表达两个 32kd 类囊体膜蛋白基因家族成员。
Plant Mol Biol. 1984 Jul;3(4):249-58. doi: 10.1007/BF00029661.
3
The amino terminal region delimited by Met1 and Met 37 is an integral part of the 32 kDa herbicide binding protein.
蓝藻聚球藻通过 D1 交换调节光系统 II 功能以响应激发胁迫。
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Minimal genomes, maximal productivity: comparative genomics of the photosystem and light-harvesting complexes in the marine cyanobacterium, Prochlorococcus.最小基因组,最大生产力:海洋蓝细菌原绿球藻中光系统和捕光复合体的比较基因组学
Photosynth Res. 2009 Jul;101(1):1-19. doi: 10.1007/s11120-009-9455-x. Epub 2009 Jun 26.
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The photosynthetic apparatus of Prochlorococcus: Insights through comparative genomics.原绿球藻的光合机构:通过比较基因组学获得的见解
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Appl Environ Microbiol. 2002 Mar;68(3):1358-66. doi: 10.1128/AEM.68.3.1358-1366.2002.
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Differential expression of the psbA genes in the cyanobacterium Synechocystis 6803.集胞藻6803中psbA基因的差异表达
Mol Gen Genet. 1993 Apr;238(1-2):161-8. doi: 10.1007/BF00279543.
8
Over-production of the D1 protein of photosystem II reaction centre in the cyanobacterium Synechococcus sp. PCC 7942.蓝藻聚球藻属PCC 7942中光系统II反应中心D1蛋白的过量产生。
Plant Mol Biol. 1994 Oct;26(2):709-21. doi: 10.1007/BF00013756.
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Characterization of the single psbA gene of Prochlorococcus marinus CCMP 1375 (Prochlorophyta).海洋原绿球藻CCMP 1375(原绿藻门)单个psbA基因的特征分析
Plant Mol Biol. 1995 Mar;27(6):1189-96. doi: 10.1007/BF00020892.
10
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Plant Mol Biol. 1989 Nov;13(5):469-79. doi: 10.1007/BF00027307.
由 Met1 和 Met37 限定的氨基末端区域是 32kDa 除草剂结合蛋白的一个组成部分。
Plant Mol Biol. 1987 Jul;8(4):337-43. doi: 10.1007/BF00021313.
4
Molecular cloning and nucleotide sequence of the psaA and psaB genes of the cyanobacterium Synechococcus sp. PCC 7002.蓝藻集胞藻 PCC 7002 的 psaA 和 psaB 基因的分子克隆和核苷酸序列。
Plant Mol Biol. 1987 Sep;9(5):453-68. doi: 10.1007/BF00015877.
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Structure of the protein subunits in the photosynthetic reaction centre of Rhodopseudomonas viridis at 3Å resolution.光合反应中心的蛋白质亚基在 3Å 分辨率下的结构。
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6
Herbicide resistance and cross-resistance: changes at three distinct sites in the herbicide-binding protein.除草剂抗性和交叉抗性:除草剂结合蛋白三个不同位点的变化。
Science. 1985 Apr 12;228(4696):204-7. doi: 10.1126/science.228.4696.204.
7
Molecular Basis of Herbicide Resistance in Amaranthus hybridus.苋菜抗除草剂的分子基础。
Science. 1983 Dec 23;222(4630):1346-9. doi: 10.1126/science.222.4630.1346.
8
Nucleotide sequence of the gene for the M(r) 32,000 thylakoid membrane protein from Spinacia oleracea and Nicotiana debneyi predicts a totally conserved primary translation product of M(r) 38,950.菠菜和烟草 M(r)32000 叶绿体膜蛋白基因的核苷酸序列预测其初级翻译产物的分子量为 38950。
Proc Natl Acad Sci U S A. 1982 Dec;79(24):7699-703. doi: 10.1073/pnas.79.24.7699.
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Photoaffinity labeling of an herbicide receptor protein in chloroplast membranes.光亲和标记叶绿体膜中的除草剂受体蛋白。
Proc Natl Acad Sci U S A. 1981 Feb;78(2):981-5. doi: 10.1073/pnas.78.2.981.
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Transformation in Agmenellum quadruplicatum.Agmenellum quadruplicatum 的转化。
Proc Natl Acad Sci U S A. 1980 Oct;77(10):6052-6. doi: 10.1073/pnas.77.10.6052.