Crystal structure of a KSHV-SOX-DNA complex: insights into the molecular mechanisms underlying DNase activity and host shutoff

被引:32
作者
Bagneris, Claire [1 ]
Briggs, Louise C. [1 ]
Savva, Renos [1 ]
Ebrahimi, Bahram [2 ]
Barrett, Tracey E. [1 ]
机构
[1] Univ London Birkbeck Coll, Dept Biol Sci, Inst Struct & Mol Biol, London WC1E 7HX, England
[2] Univ Liverpool, Inst Integrat Biol, Liverpool L69 7ZB, Merseyside, England
基金
英国医学研究理事会;
关键词
SIMPLEX-VIRUS TYPE-1; SARCOMA-ASSOCIATED HERPESVIRUS; ALKALINE NUCLEASE; KB CELLS; ENDONUCLEASE; EXONUCLEASE; PROTEIN; REPLICATION; RECOGNITION; PURIFICATION;
D O I
10.1093/nar/gkr111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The early lytic phase of Kaposi's sarcoma herpesvirus infection is characterized by viral replication and the global degradation (shutoff) of host mRNA. Key to both activities is the virally encoded alkaline exonuclease KSHV SOX. While the DNase activity of KSHV SOX is required for the resolution of viral genomic DNA as a precursor to encapsidation, its exact involvement in host shutoff remains to be determined. We present the first crystal structure of a KSHV SOX-DNA complex that has illuminated the catalytic mechanism underpinning both its endo and exonuclease activities. We further illustrate that KSHV SOX, similar to its Epstein-Barr virus homologue, has an intrinsic RNase activity in vitro that although an element of host shutoff, cannot solely account for the phenomenon.
引用
收藏
页码:5744 / 5756
页数:13
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