ライフサイエンスコーパス: BYV

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1 he dual function of p64 in tail assembly and BYV motility and support the concept of the virion tail

2 roteinase efficiently processed the chimeric BYV polyprotein in vitro.

3 to rescue the amplification of the chimeric BYV variants.

4 th cDNA clone of beet yellows closterovirus (BYV) was engineered and used to map functions involved i

5 l infection, the beet yellows closterovirus (BYV) was modified to express green fluorescent protein.

6 ividual genes of beet yellows closterovirus (BYV).

7 the virion tail as a specialized device for BYV cell-to-cell movement.

8 vement-deficient phenotypes were observed in BYV variants possessing HSP70h that lacked the computer-

9 ong 10 open reading frames (ORFs) present in BYV, ORFs 1a and 1b suffice for RNA replication and tran

10 Examination of the role of L-Pro in BYV cell-to-cell movement revealed that none of the 20 e

11 here that the Hsp70h interacts with a 20-kDa BYV protein (p20).

12 of 493 codons resulted in complete arrest of BYV translocation from cell to cell.

13 in (p64) is the fourth integral component of BYV virions.

14 le for assembly and cell-to-cell movement of BYV but is required for the long-distance transport of v

15 were observed for the leader proteinases of BYV, CTV, and LIYV.

16 ta indicated that the temporal regulation of BYV gene expression includes early (HSP70h, CPm, CP, and

17 ions affected the long-distance transport of BYV to various degrees, whereas three mutations complete

18 ccumulation compared to that of the parental BYV.

19 e kinetics of transcription of the remaining BYV genes encoding a 64-kDa protein (p64), a minor capsi

20 ed functions of L-Pro, it also serves as the BYV long-distance transport factor.

21 Six full-length myosin cDNAs from the BYV host plant Nicotiana benthamiana were sequenced and

22 Similar analyses of the BYV hybrids, in which only the papain-like domain of L-P

23 F between the first and second codons of the BYV ORFs encoding the HSP70 homolog (HSP70h), a major ca

24 biochemical analyses, we show here that the BYV 64-kDa protein (p64) is the fourth integral componen

25 oci similar to those formed by the wild-type BYV.

26 ion of the closterovirus Beet yellows virus (BYV) consists of a long body formed by the major capsid

27 sp70 homolog (Hsp70h) of Beet yellows virus (BYV) functions in virion assembly and cell-to-cell movem

28 -to-cell movement of the Beet yellows virus (BYV) is mediated by a movement protein that is an Hsp70

29 roteinase (L-Pro) of the Beet yellows virus (BYV) possesses a nonconserved N-terminal domain and a co

30 er proteinase (L-Pro) of Beet yellows virus (BYV; a closterovirus) was replaced with L1 or L2 protein

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