ライフサイエンスコーパス: potato virus X

1 e the spread of Tomato bushy stunt virus and Potato virus X.

2 hy stunt virus, Cucumber necrosis virus, and Potato virus X.

3 epeats (LRR) that confers resistance against Potato virus X.

4 erived effector protein, the coat protein of potato virus X.

5 aused loss of Rx-mediated resistance against potato virus X and N-mediated tobacco mosaic virus resis

6 APII were resistant to tobacco mosaic virus, potato virus X and the fungal pathogen Rhizoctonia solan

7 on two distinct movement-defective viruses, Potato virus X and Turnip crinkle virus, and an agroinfi

8 allenged with three viruses: potato virus Y, potato virus X, and tobacco mosaic virus.

9 us; to confirm the symmetry of a potexvirus, potato virus X; and to determine the low-resolution stru

10 Here we exploit Potato virus X as a tool for virus-induced gene compleme

11 NAs and remain stable when incorporated into potato virus X-based viral vectors for art-sRNA-mediated

12 nscription factors, we demonstrate that this Potato virus X-based virus-induced gene reprogramming st

13 Recombinant Potato virus X bearing FT RNA spread and established sys

14 In the present study, we describe a Potato virus X-derived vector that, upon agroinfection i

15 oiled coil (CC) type sensor NLRs such as the Potato virus X disease resistance protein Rx have been s

16 tag for purification, was incorporated into Potato virus X for transient expression in Nicotiana ben

17 on response, including extreme resistance to Potato virus X in potato shoots.

18 Phloem sieve elements and xylem vessels from Potato virus X-infected plants also contained lipid-asso

19 obamovirus, but not Cucumber mosaic virus or Potato virus X, infection of N. tabacum plants resulted

20 thermore, SPRYSEC-19 abrogated resistance to Potato virus X mediated by the CC-NB-LRR resistance prot

21 genus), but not to Cucumber mosaic virus and Potato virus X (members of different genera than the tob

22 ion abolish StREM1.3 function in restricting potato virus X movement.

23 heat protein A-gliadin and the plant viruses potato virus X, narcissus mosaic virus, papaya mosaic vi

24 bamovirus, turnip vein clearing tobamovirus, potato virus X potexvirus, or turnip mosaic potyvirus.

25 y to achieve this goal was the production of potato virus X (PVX) "amplicon" lines: transgenic lines

26 lio recognition sequences into the genome of potato virus X (PVX) allowed the PVX RNA to be localized

27 ) was downregulated following infection with potato virus X (PVX) and that NbFD1 regulates callose de

28 For the potexvirus Potato virus X (PVX) and the potyvirus Plum pox virus (P

29 n components from a filamentous plant virus, potato virus X (PVX) as an RNA platform delivery technol

30 Here we show that Potato virus X (PVX) can infect Arabidopsis (Arabidopsis

31 Transgenic expression of a replicating potato virus X (PVX) construct (termed an 'amplicon') re

32 Potato virus X (PVX) does not systemically infect Arabid

33 erium tumefaciens binary vector carrying the potato virus X (PVX) genome.

34 kDa, bind to a site within the 3' region of potato virus X (PVX) genomic RNA.

35 Infection with Potato virus X (PVX) in Nicotiana benthamiana plants lea

36 to analyze cis-acting sequences required for potato virus X (PVX) replication.

37 Potato virus X (PVX) requires three virally encoded prot

38 The 72nt 3' non-translated region (NTR) of potato virus X (PVX) RNA is identical in all sequenced P

39 2 (SL2; nt 143-183), within the 5' 230 nt of potato virus X (PVX) RNA.

40 hich the transgene was a cDNA of replicating potato virus X (PVX) RNA.

41 orescent protein (GFP) gene was fused to the potato virus X (PVX) TGBp2 gene, inserted into either th

42 expressed individually from the heterologous potato virus X (PVX) vector, both proteins preferentiall

43 Using a recombinant potato virus X (PVX) vector, we investigated the relatio

44 n resistant or susceptible plant lines via a potato virus X (PVX) vector.

45 lls expressing TGB2, one of the three MPs of Potato virus X (PVX), and in PVX-infected cells, suggest

46 nts infected with the plus-strand RNA virus, potato virus X (PVX), supported synthesis of four major,

47 applied to tobacco leaves in the presence of potato virus X (PVX), the C-terminal deletion mutant had

48 sum) Rx protein, which confers resistance to Potato virus X (PVX), to investigate the function of the

49 ifferent genera [tobacco mosaic virus (TMV), potato virus X (PVX), tomato bushy stunt virus (TBSV)],

50 onfers resistance against a single strain of potato virus X (PVX), whereas LRR mutants protect agains

51 -LRR protein of potato confers resistance to potato virus X (PVX).

52 Rx2 confers resistance against potato virus X (PVX).

53 virus (CMV), but not in plants infected with potato virus X (PVX).

54 as the triple gene block (TGB), typified by Potato virus X (PVX).

55 In potato virus X (PVX)/potyviral synergism, increased path

56 ) to the cyst nematode Globodera pallida and Potato virus X, respectively.

57 e potato cyst nematode Globodera pallida and Potato virus X, respectively.

58 After infection by a strain of potato virus X that does not spread in wild-type tobacco

59 otiana benthamiana when overexpressed from a Potato virus X vector and that reversal of TGS by gemini

60 The ability of a potato virus X vector expressing green fluorescent prote

61 sed from the same vector or from coinfecting potato virus X vectors.

62 (ACMV) and a gene expression vector based on Potato virus X were exploited to devise an in planta sys

63 NbGlk1 activates cellular responses to potato virus X, whereas Rx1 associates with NbGlk1 and p

64 at confer resistance, in Solanum species, to potato viruses X, Y, A and V (the viruses for which the