Epstein-Barr virus and virus human protein interaction maps

被引:289
作者
Calderwood, Michael A.
Venkatesan, Kavitha
Xing, Li
Chase, Michael R.
Vazquez, Alexel
Holthaus, Amy M.
Ewence, Alexandra E.
Li, Ning
Hirozane-Kishikawa, Tomoko
Hill, David E.
Vidal, Marc [1 ]
Kieff, Elliott
Johannsen, Eric
机构
[1] Harvard Univ, Sch Med, Channing Lab, Program Virol,Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Channing Lab, Program Virol,Dept Microbiol & Mol Genet, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Ctr Canc Syst Biol, Boston, MA 02115 USA
[6] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[7] Inst Adv Studies, Simons Ctr Syst Biol, Princeton, NJ 08540 USA
关键词
herpesvirus; interactome; replication; yeast two hybrid;
D O I
10.1073/pnas.0702332104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A comprehensive mapping of interactions among Epstein-Barr virus (EBV) proteins and interactions of EBV proteins with human proteins should provide specific hypotheses and a broad perspective on EBV strategies for replication and persistence. Interactions of EBV proteins with each other and with human proteins were assessed by using a stringent high-throughput yeast two-hybrid system. Overall, 43 interactions between EBV proteins and 173 interactions between EBV and human proteins were identified. EBV-EBV and EBV-human protein interaction, or '' interactome '' maps provided a framework for hypotheses of protein function. For example, LF2, an EBV protein of unknown function interacted with the EBV immediate early R transactivator (Rta) and was found to inhibit Rta transactivation. From a broader perspective, EBV genes can be divided into two evolutionary classes, '' core '' genes, which are conserved across all herpesviruses and subfamily specific, or '' noncore '' genes. Our EBV-EBV interactome map is enriched for interactions among proteins in the same evolutionary class. Furthermore, human proteins targeted by EBV proteins were enriched for highly connected or '' hub '' proteins and for proteins with relatively short paths to all other proteins in the human interactome network. Targeting of hubs might be an efficient mechanism for EBV reorganization of cellular processes.
引用
收藏
页码:7606 / 7611
页数:6
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