期刊
JOURNAL OF VIROLOGY
卷 74, 期 12, 页码 5726-5728出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.74.12.5726-5728.2000
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资金
- NIAID NIH HHS [AI26538, R01 AI026538] Funding Source: Medline
A herpes simplex virus type 1 (HSV-1) Ori(S) analogue in which the A+T sequence linking: the box I and II elements was replaced by two single-stranded oligo(dT)s is unwound by the UL9 protein ICP8 complex. Unwinding of wild-type Ori(S) by the UL9 protein-ICP8 complex was also observed under conditions which destabilize the A+T sequence. These experiments support a model for the unwinding of Ori(S) in which destabilization of the A+T sequence can generate a single-stranded DNA binding site for ICP8, which then associates with the UL9 protein bound to boxes I and II to promote the bidirectional unwinding of Ori(S).
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