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In vitro characterisation of the MS2 RNA polymerase complex reveals host factors that modulate emesviral replicase activity
by
Wagner, Alexander
, Weise, Laura I.
, Mutschler, Hannes
in
38/23
/ 45/29
/ 45/77
/ 45/90
/ 631/326/1321
/ 631/326/432
/ 631/45/500
/ 82/83
/ Biology
/ Biomedical and Life Sciences
/ DNA-directed RNA polymerase
/ DNA-Directed RNA Polymerases - metabolism
/ Gene expression
/ Initiation factors
/ Levivirus
/ Life Sciences
/ Peptide Elongation Factor Tu - metabolism
/ Phages
/ Q beta Replicase - chemistry
/ Q beta Replicase - metabolism
/ Replicase
/ Replication
/ Ribosomal protein S1
/ RNA
/ RNA phages
/ RNA polymerase
2022
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In vitro characterisation of the MS2 RNA polymerase complex reveals host factors that modulate emesviral replicase activity
by
Wagner, Alexander
, Weise, Laura I.
, Mutschler, Hannes
in
38/23
/ 45/29
/ 45/77
/ 45/90
/ 631/326/1321
/ 631/326/432
/ 631/45/500
/ 82/83
/ Biology
/ Biomedical and Life Sciences
/ DNA-directed RNA polymerase
/ DNA-Directed RNA Polymerases - metabolism
/ Gene expression
/ Initiation factors
/ Levivirus
/ Life Sciences
/ Peptide Elongation Factor Tu - metabolism
/ Phages
/ Q beta Replicase - chemistry
/ Q beta Replicase - metabolism
/ Replicase
/ Replication
/ Ribosomal protein S1
/ RNA
/ RNA phages
/ RNA polymerase
2022
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In vitro characterisation of the MS2 RNA polymerase complex reveals host factors that modulate emesviral replicase activity
by
Wagner, Alexander
, Weise, Laura I.
, Mutschler, Hannes
in
38/23
/ 45/29
/ 45/77
/ 45/90
/ 631/326/1321
/ 631/326/432
/ 631/45/500
/ 82/83
/ Biology
/ Biomedical and Life Sciences
/ DNA-directed RNA polymerase
/ DNA-Directed RNA Polymerases - metabolism
/ Gene expression
/ Initiation factors
/ Levivirus
/ Life Sciences
/ Peptide Elongation Factor Tu - metabolism
/ Phages
/ Q beta Replicase - chemistry
/ Q beta Replicase - metabolism
/ Replicase
/ Replication
/ Ribosomal protein S1
/ RNA
/ RNA phages
/ RNA polymerase
2022
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In vitro characterisation of the MS2 RNA polymerase complex reveals host factors that modulate emesviral replicase activity
Journal Article
In vitro characterisation of the MS2 RNA polymerase complex reveals host factors that modulate emesviral replicase activity
2022
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Overview
The RNA phage MS2 is one of the most important model organisms in molecular biology and virology. Despite its comprehensive characterisation, the composition of the RNA replication machinery remained obscure. Here, we characterised host proteins required to reconstitute the functional replicase in vitro. By combining a purified replicase sub-complex with elements of an in vitro translation system, we confirmed that the three host factors, EF-Ts, EF-Tu, and ribosomal protein S1, are part of the active replicase holocomplex. Furthermore, we found that the translation initiation factors IF1 and IF3 modulate replicase activity. While IF3 directly competes with the replicase for template binding, IF1 appears to act as an RNA chaperone that facilitates polymerase readthrough. Finally, we demonstrate in vitro formation of RNAs containing minimal motifs required for amplification. Our work sheds light on the MS2 replication machinery and provides a new promising platform for cell-free evolution.
Host proteins are identified which are required to reconstitute a functional RNA phage MS2 replication machinery, providing a promising platform for cell-free gene expression.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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