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Cauliflower Mosaic Virus Gene VI Controls Translation from Dicistronic Expression Units in Transgenic Arabidopsis Plants.花椰菜花叶病毒基因VI调控转基因拟南芥植株中双顺反子表达单元的翻译。
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Analysis of the cDNAs of hypothetical genes on Arabidopsis chromosome 2 reveals numerous transcript variants.对拟南芥2号染色体上假定基因的cDNA分析揭示了众多转录变体。
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7
Arabidopsis mutants that suppress the phenotype induced by transgene-mediated expression of cauliflower mosaic virus (CaMV) gene VI are less susceptible to CaMV-infection and show reduced ethylene sensitivity.抑制由转基因介导的花椰菜花叶病毒(CaMV)基因VI表达所诱导的表型的拟南芥突变体对CaMV感染的敏感性较低,且乙烯敏感性降低。
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Auxin acts in xylem-associated or medullary cells to mediate apical dominance.生长素在与木质部相关的细胞或髓细胞中起作用,以介导顶端优势。
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Viral strategies of translation initiation: ribosomal shunt and reinitiation.病毒的翻译起始策略:核糖体移码和重新起始。
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本文引用的文献

1
The Cauliflower Mosaic Virus 35S Promoter: Combinatorial Regulation of Transcription in Plants.花椰菜花叶病毒35S启动子:植物转录的组合调控
Science. 1990 Nov 16;250(4983):959-66. doi: 10.1126/science.250.4983.959.
2
Cauliflower mosaic virus gene VI produces a symptomatic phenotype in transgenic tobacco plants.花椰菜花叶病毒基因 VI 在转基因烟草植物中产生症状表型。
Proc Natl Acad Sci U S A. 1988 Feb;85(3):733-7. doi: 10.1073/pnas.85.3.733.
3
In vitro expression of cauliflower mosaic virus genes.在体外用菜花 mosaic 病毒基因表达。
EMBO J. 1988 Feb;7(2):309-17. doi: 10.1002/j.1460-2075.1988.tb02814.x.
4
Initiation of translation of the cauliflower mosaic virus genome from a polycistronic mRNA: evidence from deletion mutagenesis.花椰菜花叶病毒基因组从多顺反子 mRNA 翻译的起始:缺失突变的证据。
EMBO J. 1984 Dec 1;3(12):2731-6. doi: 10.1002/j.1460-2075.1984.tb02203.x.
5
Gene I, a potential cell-to-cell movement locus of cauliflower mosaic virus, encodes an RNA-binding protein.基因I是花椰菜花叶病毒一个潜在的细胞间运动位点,编码一种RNA结合蛋白。
Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2476-80. doi: 10.1073/pnas.88.6.2476.
6
Rapid isolation of high molecular weight plant DNA.高分子量植物DNA的快速分离
Nucleic Acids Res. 1980 Oct 10;8(19):4321-5. doi: 10.1093/nar/8.19.4321.
7
A transcriptionally active, covalently closed minichromosome of cauliflower mosaic virus DNA isolated from infected turnip leaves.从受感染的芜菁叶片中分离出的花椰菜花叶病毒DNA的转录活性共价闭合微型染色体。
Cell. 1982 Jun;29(2):395-402. doi: 10.1016/0092-8674(82)90156-8.
8
Expression of disease symptoms in cauliflower mosaic virus genomic hybrids.花椰菜花叶病毒基因组杂种中疾病症状的表达
J Mol Appl Genet. 1984;2(6):537-47.
9
In vitro synthesis of cauliflower mosaic virus DNA in viroplasms.花椰菜花叶病毒DNA在病毒原质中的体外合成。
Adv Exp Med Biol. 1984;179:113-9. doi: 10.1007/978-1-4684-8730-5_11.
10
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.

花椰菜花叶病毒基因VI调控转基因拟南芥植株中双顺反子表达单元的翻译。

Cauliflower Mosaic Virus Gene VI Controls Translation from Dicistronic Expression Units in Transgenic Arabidopsis Plants.

作者信息

Zijlstra C., Hohn T.

机构信息

Friedrich Miescher-Institut, P.O. Box 2543, CH-4002 Basel, Switzerland.

出版信息

Plant Cell. 1992 Dec;4(12):1471-1484. doi: 10.1105/tpc.4.12.1471.

DOI:10.1105/tpc.4.12.1471
PMID:12297640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC160234/
Abstract

Transformed Arabidopsis plants were used to study the effect of the cauliflower mosaic virus (CaMV) inclusion body protein on translation of dicistronic RNA. Reporter plants contain a dicistronic transcription unit with CaMV open reading frame VII (ORF VII) as the first and the [beta]-glucuronidase (GUS) reporter ORF as the second cistron. "Transactivator plants" contain CaMV ORF VI under the control of the strong CaMV 35S promoter. The transactivator plants were difficult to regenerate and showed an abnormal phenotype. Expression of GUS activity in the reporter plants was very low, but high GUS activity could be induced by introduction of gene VI, either by crossing with plants containing gene VI as a transgene or by infection with CaMV. Histological GUS assays showed that transactivation occurred in all types of tissue and at all developmental stages. The practical implications of the induction of GUS expression from the dicistronic unit by virus infection are discussed.

摘要

利用转化的拟南芥植株研究花椰菜花叶病毒(CaMV)包涵体蛋白对双顺反子RNA翻译的影响。报告植株含有一个双顺反子转录单元,其中CaMV开放阅读框VII(ORF VII)作为第一个顺反子,β-葡萄糖醛酸酶(GUS)报告基因开放阅读框作为第二个顺反子。“反式激活植株”在强CaMV 35S启动子的控制下含有CaMV ORF VI。反式激活植株难以再生,并表现出异常表型。报告植株中GUS活性的表达非常低,但通过引入基因VI可诱导高GUS活性,方法是与作为转基因含有基因VI的植株杂交或用CaMV感染。组织学GUS分析表明,反式激活发生在所有类型的组织和所有发育阶段。本文讨论了病毒感染从双顺反子单元诱导GUS表达的实际意义。