Human kinome profiling identifies a requirement for AMP-activated protein kinase during human cytomegalovirus infection

被引:71
作者
Terry, Laura J. [1 ]
Vastag, Livia [2 ,3 ]
Rabinowitz, Joshua D. [2 ,3 ]
Shenk, Thomas [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[3] Princeton Univ, Lewis Sigler Inst Integrat Genom, Princeton, NJ 08544 USA
基金
美国国家卫生研究院;
关键词
herpesvirus; siRNA; CELL STRESS RESPONSES; METABOLOMIC ANALYSIS; INHIBITION; REPLICATION; MODULATION; PATHWAYS; VIRIONS; PP28; P38;
D O I
10.1073/pnas.1200494109
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
Human cytomegalovirus (HCMV) modulates numerous cellular signaling pathways. Alterations in signaling are evident from the broad changes in cellular phosphorylation that occur during HCMV infection and from the altered activity of multiple kinases. Here we report a comprehensive RNAi screen, which predicts that 106 cellular kinases influence growth of the virus, most of which were not previously linked to HCMV replication. Multiple elements of the AMP-activated protein kinase (AMPK) pathway scored in the screen. As a regulator of carbon and nucleotide metabolism, AMPK is poised to activate many of the metabolic pathways induced by HCMV infection. An AMPK inhibitor, compound C, blocked a substantial portion of HCMV-induced metabolic changes, inhibited the accumulation of all HCMV proteins tested, and markedly reduced the production of infectious progeny. We propose that HCMV requires AMPK or related activity for viral replication and reprogramming of cellular metabolism.
引用
收藏
页码:3071 / 3076
页数:6
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