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首页> 外文期刊>Archives of Virology >The methyltransferase domain of the 1a protein of cowpea chlorotic mottle virus controls local and systemic accumulation in cowpea
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The methyltransferase domain of the 1a protein of cowpea chlorotic mottle virus controls local and systemic accumulation in cowpea

机译:cow豆褪绿斑驳病毒1a蛋白的甲基转移酶结构域控制cow豆的局部和全身积累

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摘要

The type strain of cowpea chlorotic mottle virus (CCMV-T) induces a local and systemic infection in California Blackeye cowpea (Vigna unguiculata (L.) Walp. subs. unguiculata cv. California Blackeye), but accumulates to low levels in inoculated leaves and fails to accumulate systemically in the cowpea plant introduction (PI) 186465. CCMV-R, a mutant strain derived from CCMV-T, accumulates to higher levels than CCMV-T in inoculated leaves and systemically infects PI 186465 plants. The phenotypic determinant of CCMV-R was previously mapped to viral RNA1, but the location of the determinant within RNA1 was not identified. Pseudorecombinants generated from genomic cDNA clones of CCMV-T and CCMV-R indicated that the phenotypic differences on PI 186465 were independent of replication. Through the use of chimeric RNA1 cDNA clones containing portions of CCMV-T and CCMV-R and site-directed mutagenesis, two nucleotides, 299 (amino acid residue 77) and 951 (amino acid residue 294), were identified as being independently critical for the local and systemic accumulation patterns of CCMV-R in PI 186465 plants. A second independently derived CCMV-R-like mutant, identified nucleotide 216 (amino acid residue 49) as being critical for induction of the CCMV-R infection phenotype. Amino acid residues 49, 77, and 294 are within the methytransferase domain of the CCMV 1a protein, suggesting that the methytransferase domain has a role in cell-to-cell and systemic accumulation of the virus that is independent of replication.
机译:cow豆褪绿斑驳病毒(CCMV-T)型菌株在加利福尼亚黑眼cow豆(Vigna unguiculata(L.)Walp.sub .. unguiculata cv.California Blackeye)中引起局部和全身感染,但在接种的叶片和叶片中积累到较低水平不能在plant豆植株导入(PI)186465中系统地积聚。CCMV-R(源自CCMV-T的突变株)在接种叶片中的积聚水平高于CCMV-T,并全身性感染PI 186465植物。 CCMV-R的表型行列式先前已被映射到病毒RNA1,但未确定行列式在RNA1中的位置。从CCMV-T和CCMV-R的基因组cDNA克隆产生的伪重组体表明PI 186465的表型差异与复制无关。通过使用包含CCMV-T和CCMV-R部分的嵌合RNA1 cDNA克隆以及定点诱变,鉴定出两个核苷酸299(氨基酸残基77)和951(氨基酸残基294)对于PI 186465植物中CCMV-R的局部和全身积累模式。第二个独立衍生的CCMV-R样突变体鉴定出核苷酸216(氨基酸残基49)对于诱导CCMV-R感染表型至关重要。氨基酸残基49、77和294位于CCMV 1a蛋白的甲基转移酶结构域内,这表明甲基转移酶结构域在病毒的细胞间和系统性积累中具有独立于复制的作用。

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  • 来源
    《Archives of Virology 》 |2008年第8期| 1505-1516| 共12页
  • 作者单位

    Department of Plant Pathology Plant Sciences Building The University of Georgia Athens GA 30602-7274 USA;

    Plant Biology Division The Samuel Roberts Noble Foundation P.O. Box 2180 Ardmore OK 73410 USA;

    Department of Plant Pathology Plant Sciences Building The University of Georgia Athens GA 30602-7274 USA;

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