2016
DOI: 10.1038/srep32445
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Analysis of Sogatella furcifera proteome that interact with P10 protein of Southern rice black-streaked dwarf virus

Abstract: Southern rice black-streaked dwarf virus (SRBSDV) is transmitted efficiently only by white-backed planthopper (WBPH, Sogatella furcifera) in a persistent propagative manner. Here we used a yeast two-hybrid system to investigate the interactions between the SRBSDV- P10 and the cDNA library of WBPH. Of 130 proteins identified as putative interactors, 28 were further tested in a retransformation analysis and β-galactosidase assay to confirm the interaction. The full-length gene sequences of 5 candidate proteins: … Show more

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Cited by 18 publications
(22 citation statements)
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“…As with virus infection, extreme temperatures, or insecticide treatment, each stress could lead to the change in the expression patterns in WBPH, and these results provide a valuable resource for the molecular characterization of stress action in WBPH [ 17 , 25 , 34 ]. Moreover, Than et al investigated the protein–protein interactions between SRBSDV and WBPH [ 35 ]. They identified over 100 WBPH proteins as putative interactors of the coat protein of SRBSD, which helped increase the understanding about how SRBSDV affects its insect vector.…”
Section: Discussionmentioning
confidence: 99%
“…As with virus infection, extreme temperatures, or insecticide treatment, each stress could lead to the change in the expression patterns in WBPH, and these results provide a valuable resource for the molecular characterization of stress action in WBPH [ 17 , 25 , 34 ]. Moreover, Than et al investigated the protein–protein interactions between SRBSDV and WBPH [ 35 ]. They identified over 100 WBPH proteins as putative interactors of the coat protein of SRBSD, which helped increase the understanding about how SRBSDV affects its insect vector.…”
Section: Discussionmentioning
confidence: 99%
“…qRT-PCR was performed using the Roche LightCycler ® 480II. The thermal cycling program was as follows5758: 95 °C for 15 min, 40 cycles at 95 °C for 15 s and at 60 °C for 30 s. The gene expression of rice UBQ5 was used as an internal control.…”
Section: Methodsmentioning
confidence: 99%
“…To verify the presence of viruses in field samples, we used RT-PCR and specific primers designed on the sequences of assembled contigs (Table S4 ). The sequences of the extreme ends of the genomic RNAs were determined employing the 5′- and 3′-RACE System for Rapid Amplification of cDNA Ends kits (Thermo Fisher Scientific, Waltham, MA, USA) (Than et al, 2016 ). The primers and other oligonucleotides used for RT-PCR and RACE analyses are listed in Table S3 .…”
Section: Methodsmentioning
confidence: 99%