Abstract
The origin of microbial mercury methylation has long been a mystery. Here, we employed genome-resolved phylogenetic analyses to decipher the evolution of the mercury-methylating gene, hgcAB, constrain the ancestral origin of the hgc operon, and explain the distribution of hgc in Bacteria and Archaea. We infer the extent to which vertical inheritance and horizontal gene transfer have influenced the evolution of mercury methylators and hypothesize that evolution of this trait bestowed the ability to produce an antimicrobial compound (MeHg+) on a potentially resource-limited early Earth. We speculate that, in response, the evolution of MeHg+-detoxifying alkylmercury lyase (encoded by merB) reduced a selective advantage for mercury methylators and resulted in widespread loss of hgc in Bacteria and Archaea.
| Original language | English |
|---|---|
| Journal | Genome biology and evolution |
| Volume | 15 |
| Issue number | 4 |
| Early online date | 23 Mar 2023 |
| DOIs | |
| Publication status | Published - 6 Apr 2023 |
Data Availability Statement
All data generated in this study including amino acid alignments and phylogenetic trees are deposited in Figshare: https://doi.org/10.6084/m9.figshare.21428523.Acknowledgements
We thank Yao-ban Chan and Qiuyi Li at The University of Melbourne for valuable discussions and advice in the early stage of this study. We also acknowledge helpful discussions with Caitlin Gionfriddo, Ben Peterson, and Eric Capo.Funding
This publication was made possible in part through support from a Strategic Australian Postgraduate Award (PhD scholarship) to H.L. from the Environmental Microbiology Research Initiative (EMRI) at The University of Melbourne (J.W.M.) and laboratory start-up funding from the University of Glasgow to J.W.M., the Moore Foundation (https://doi.org/10.37807/GBMF9741 to T.A.W.), the Royal Society (URF\R\201024) to T.A.W., and the John Templeton Foundation (62220 to T.A.W. and E.R.R.M.). The opinions expressed in this publication are those of the author(s) and do not necessarily reflect the views of the John Templeton Foundation.
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