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The self-interaction of a nodavirus replicase is enhanced by mitochondrial membrane lipids.


ABSTRACT: RNA replication of positive-strand (+)RNA viruses requires the protein-protein interactions among viral replicases and the association of viral replicases with intracellular membranes. Protein A from Wuhan nodavirus (WhNV), which closely associate with mitochondrial membranes, is the sole replicase required for viral RNA replication. Here, we studied the direct effects of mitochondrial membrane lipids (MMLs) on WhNV protein A activity in vitro. Our investigations revealed the self-interaction of WhNV protein A is accomplished via two different patterns (i.e., homotypic and heterotypic self-interactions via different interfaces). MMLs stimulated the protein A self-interaction, and this stimulation exhibited selectivity for specific phospholipids. Moreover, we found that specific phospholipids differently favor the two self-interaction patterns. Furthermore, manipulating specific phospholipid metabolism affected protein A self-interaction and the activity of protein A to replicate RNA in cells. Taken together, our findings reveal the direct effects of membrane lipids on a nodaviral RNA replicase.

SUBMITTER: Qiu Y 

PROVIDER: S-EPMC3934934 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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The self-interaction of a nodavirus replicase is enhanced by mitochondrial membrane lipids.

Qiu Yang Y   Wang Zhaowei Z   Liu Yongxiang Y   Han Yajuan Y   Miao Meng M   Qi Nan N   Yang Jie J   Xia Hongjie H   Li Xiaofeng X   Qin Cheng-Feng CF   Hu Yuanyang Y   Zhou Xi X  

PloS one 20140225 2


RNA replication of positive-strand (+)RNA viruses requires the protein-protein interactions among viral replicases and the association of viral replicases with intracellular membranes. Protein A from Wuhan nodavirus (WhNV), which closely associate with mitochondrial membranes, is the sole replicase required for viral RNA replication. Here, we studied the direct effects of mitochondrial membrane lipids (MMLs) on WhNV protein A activity in vitro. Our investigations revealed the self-interaction of  ...[more]

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