共 23 条
Functional Insights into ANP32A-Dependent Influenza A Virus Polymerase Host Restriction
被引:58
作者:

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机构:

Hale, Benjamin G.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Zurich, Inst Med Virol, Winterthurerstr 190, CH-8057 Zurich, Switzerland Univ Zurich, Inst Med Virol, Winterthurerstr 190, CH-8057 Zurich, Switzerland
机构:
[1] Univ Zurich, Inst Med Virol, Winterthurerstr 190, CH-8057 Zurich, Switzerland
基金:
欧洲研究理事会;
关键词:
AMINO-ACID;
RIG-I;
SUMOYLATION;
ADAPTATION;
COMPLEX;
MANNER;
RANGE;
D O I:
10.1016/j.celrep.2017.08.061
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Host restriction of influenza A virus limits pandemic emergence. The viral RNA polymerase (vPol) is an essential enzyme that must adapt for avian viruses to replicate in humans. Species differences in host ANP32A dictate adaptation: human ANP32A lacks an uncharacterized 33 amino-acid insertion that is present in avian ANP32A. Here, we uncover important contributions of host SUMOylation to vPol activity, including avANP32A function. We also identify a hydrophobic SUMO interaction motif (SIM)-like sequence unique to avANP32A that critically supports avian-signature vPol. Unrelated SIM sequences partially recapitulate this function when introduced into huANP32A. By investigating ANP32A-vPol interactions, we find that huANP32A interacts weakly with both human-and avian-signature vPols, while the hydrophobic motif of avANP32A promotes stronger interactions. Furthermore, we identify a highly acidic stretch in avANP32A that constitutes a major site of vPol interaction. Our data suggest compensatory mechanisms underlying vPol adaptation to host ANP32A independent of species-specific interactions.
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页码:2538 / 2546
页数:9
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