Characterization of the in vitro Activities of the P1 and Helper Component Proteases of Soybean mosaic virus Strain G2 and Tobacco vein mottling virus

被引:0
作者
Lim, Hyoun-Sub [2 ]
Jang, Chan-Yong [2 ]
Nam, Jiryun [2 ]
Li, Meijia [2 ]
Hong, Jin-Sung [3 ]
Bae, Hanhong [4 ]
Ju, Ho-Jong [5 ]
Kim, Hong Gi [2 ]
Ford, Richard E. [1 ]
Domier, Leslie L. [1 ,6 ]
机构
[1] Univ Illinois, Dept Crop Sci, Urbana, IL 61801 USA
[2] Chungnam Natl Univ, Dept Appl Biol, Taejon 305764, South Korea
[3] Seoul Womans Univ, Inst Nat Sci, Seoul 139774, South Korea
[4] Yeungnam Univ, Sch Biotechnol, Kyongsan 712749, South Korea
[5] Chonbuk Natl Univ, Dept Agr Biol, Jonju 561756, South Korea
[6] ARS, USDA, Urbana, IL 61801 USA
关键词
Helper-component protease; in vitro translation; P1; protease; trypsin inhibitor; DIFFERENTIAL EXPRESSION; TRYPSIN-INHIBITORS; HC-PRO; POTYVIRUS; PLANT; KUNITZ;
D O I
10.5423/PPJ.2012.28.2.197
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Potyviruses express their RNA genomes through the production of polyproteins that are processed in host cells by three virus-encoded proteases. Soybean plants produce large amounts of protease inhibitors during seed development and in response to wounding that could affect the activities of these proteases. The in vitro activities of two of the proteases of Soybean mosaic virus (SMV) and Tobacco vein mottling virus (TVMV) were compared in the rabbit reticulocyte lysate in vitro translation system using synthetic RNA transcripts. Transcripts produced from SMV and TVMV cDNAs that included the P1 and helper component-protease (HC-Pro) coding regions directed synthesis of protein products that were only partially processed. Unprocessed polyproteins were not detected from transcripts that included all of the P1, HC-Pro, P3 and portions of the cylindrical inclusion protein coding regions of either virus. Addition of soybean trypsin inhibitor to in vitro translation reactions increased the accumulation of the unprocessed polyprotein from TVMV transcripts, but did not alter the patterns of proteins produced from SMV. These experiments suggest that SMV- and TVMV-encoded proteases are differentially sensitive to protease inhibitors.
引用
收藏
页码:197 / 201
页数:5
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