ライフサイエンスコーパス: potyvirus

1 d HC-Pro proteinase of Tobacco etch virus (a potyvirus).

2 be fulfilled by the HCPro of a heterologous potyvirus.

3 with aphid transmitted species of the genus Potyvirus.

4 potato virus X potexvirus, or turnip mosaic potyvirus.

5 mosaic virus (TuMV), a positive-stranded RNA potyvirus.

6 ssively inherited resistance against several potyviruses.

7 information on the translational strategy of potyviruses.

8 role normally associated with HCPro in other potyviruses.

9 tibility was named loss-of-susceptibility to potyviruses 1 (lsp1).

10 been characterized for viruses in the genera Potyvirus and Caulimovirus.

11 tifunctional protein of members of the genus Potyvirus and other viruses of the family Potyviridae.

12 new target for seeking natural resistance to potyviruses and new opportunities for the control of pot

13 The P1/HC-Pro sequence of plant potyviruses and the 2b gene of the cucumber mosaic virus

14 mosaic necrosis virus, several other related potyviruses, and one comovirus.

15 Three protease:cleavage site pairs from Potyvirus are shown to be orthogonal and active in expos

16 otato virus Y (PVY) and potato virus A (PVA) potyviruses are helically constructed filaments that are

17 ng ribonucleoprotein complexes to facilitate potyvirus cell-to-cell movement.

18 The potyvirus cylindrical inclusion (CI) protein, an RNA hel

19 Taken together, these results suggest that potyviruses dynamically respond to the presence of their

20 Although both tritimoviruses and potyviruses encode helper component-proteinase (HC-Pro)

21 cysteine residues that are conserved in the potyvirus-encoded HC-Pro raises the possibility that the

22 Cys(72)] with the N-terminal portion of the potyvirus-encoded helper component-proteinase (HC-Pro),

23 potato feathery mottle virus (SPFMV) (genus Potyvirus, family Potyviridae) contains a large open rea

24 Potyviruses form one of the most numerous groups of plan

25 Potyvirus genome linked protein, VPg, interacts with tra

26 The Ros1 marker remained stable within the potyvirus genome through successive infectious passages

27 sistance to a number of plant viruses in the Potyvirus genus has been found to be based on mutations

28 ecessive resistances to plant viruses in the Potyvirus genus have been found to be based on mutations

29 for resistance to soybean mosaic virus (SMV; Potyvirus) has previously been described as a single-loc

30 Its causal agent, Plum pox virus (PPV; genus Potyvirus), has been classified as a quarantine pathogen

31 nd small-insertion mutations introduced into potyvirus HC-Pro.

32 Gene products of potyviruses include P1, HCPro, P3, 6K1, CI, 6K2, VPg/NIa

33 monstrate accurate tracking of turnip mosaic potyvirus infecting Arabidopsis (Arabidopsis thaliana) a

34 evidence for a direct role of CI protein in potyvirus intercellular movement, and for distinct roles

35 nces, provide a more complete picture of the potyvirus life cycle.

36 Our results show that some of the potyvirus particles contain a protruding tip at one end

37 ility factor required for infection with the Potyvirus, Pea seed-borne mosaic virus.

38 the potexvirus Potato virus X (PVX) and the potyvirus Plum pox virus (PPV), the efficiency of both V

39 that although a chimeric virus based on the potyvirus Plum pox virus lacking HCPro, which was replac

40 oved, and this phenomenon occurs for another potyvirus, Potato virus Y, suggesting a conserved role f

41 The tobacco etch potyvirus protein, helper component-proteinase (HC-Pro),

42 onal function of NIa-Pro, a highly conserved potyvirus protein.

43 ith the replication of pea seed-borne mosaic potyvirus (PSbMV).

44 e of the blotch isolate of the peanut stripe potyvirus (PStV) RNA genome was constructed downstream f

45 ns, together with related findings for other potyvirus recessive resistances, provide a more complete

46 Using two different tobacco etch potyvirus recombinant clones tagged with Ros1, we show t

47 1 locus in Capsicum result in broad-spectrum potyvirus resistance attributed to the pvr1 resistance a

48 eviously characterized dominant or recessive potyvirus resistance genes.

49 may be necessary, but is not sufficient for potyvirus resistance in vivo.

50 at disrupted cap binding is not required for potyvirus resistance.

51 ity of known soybean genes for resistance to potyviruses (Rsv1 and Rpv), Phytophthora root rot (Rps1,

52 ired for nonpersistent aphid transmission of potyviruses), sequence conservation is low (amino acid i

53 on microscopy to determine the symmetry of a potyvirus, soybean mosaic virus; to confirm the symmetry

54 elper component-proteinase (HC-Pro) of plant potyviruses suppresses PTGS in plants.

55 elper component-proteinase (HC-Pro) of plant potyviruses suppresses PTGS.

56 The avirulence determinant in this potyvirus system has previously been identified as VPg,

57 The Arabidopsis thaliana-potyvirus system was developed to identify compatibility

58 terminal 350 nucleotides of the tobacco etch potyvirus (TEV) genome span the end of the capsid protei

59 ) and the CP coding sequence of tobacco etch potyvirus (TEV) in genome amplification were analyzed.

60 host functions involved in the tobacco etch potyvirus (TEV) infection process, a tobacco line (V20)

61 Recently, we evolved tobacco etch potyvirus (TEV) lineages on different ecotypes of Arabid

62 The NIb protein of tobacco etch potyvirus (TEV) possesses several functions, including R

63 The tobacco etch potyvirus (TEV) RNA-dependent RNA polymerase (NIb) has b

64 ions fixed during adaptation of tobacco etch potyvirus (TEV) to a new experimental host, Arabidopsis

65 ith increased susceptibility to Tobacco etch potyvirus (TEV) were isolated previously, revealing a vi

66 t the long-distance movement of tobacco etch potyvirus (TEV) without involving either hypersensitive

67 on of long-distance movement of tobacco etch potyvirus (TEV).

68 e genomic RNA of tobacco etch virus (TEV), a potyvirus that belongs to the picornavirus superfamily,

69 Interestingly, while in other potyviruses the suppressor of RNA silencing is HCPro, we

70 th decreased susceptibility to Turnip mosaic potyvirus (TuMV) were isolated.

71 e we report broad-spectrum resistance to the potyvirus Turnip mosaic virus (TuMV) due to a natural me

72 tural, monogenic recessive resistance to the Potyvirus Turnip mosaic virus (TuMV) has been found in a

73 -Pro with homologues of an aphid transmitted potyvirus (Turnip mosaic virus), a rymovirus (Agropyron

74 ses and new opportunities for the control of potyviruses using genome editing techniques targeted on

75 iciviruses, like those of picornaviruses and potyviruses, utilizes tyrosine in the formation of a cov

76 nvestigate the functions of the tobacco etch potyvirus VPg-proteinase (NIa) protein in vivo.

77 inase domain (Pro) derived from tobacco etch potyvirus was utilized for tagging individual genes of b

78 i (Aac), Chilli veinal mottle virus (ChiVMV, potyvirus), Watermelon silver mottle virus (WSMoV, tospo

79 c), chilli vein-banding mottle virus (CVbMV, potyvirus), watermelon silver mottle virus (WSMoV, tospo

80 O is specific to some sweet potato-infecting potyviruses, while PIPO is present in all potyvirids.