DNA Polymerase Diversity Reveals Multiple Incursions of Polintons During Nematode Evolution

Author:

Jeong Dae-Eun1ORCID,Sundrani Sameer23ORCID,Hall Richard Nelson2,Krupovic Mart4ORCID,Koonin Eugene V5ORCID,Fire Andrew Z16ORCID

Affiliation:

1. Department of Pathology, Stanford University School of Medicine , Stanford, CA , USA

2. Department of Bioengineering, Stanford University , Stanford, CA , USA

3. Department of Biomedical Informatics, Vanderbilt University School of Medicine Present address: , Nashville, TN , USA

4. Institut Pasteur, Université Paris Cité, Archaeal Virology Unit , Paris , France

5. National National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health , Bethesda, MD , USA

6. Department of Genetics, Stanford University School of Medicine , Stanford, CA , USA

Abstract

Abstract Polintons are double-stranded DNA, virus-like self-synthesizing transposons widely found in eukaryotic genomes. Recent metagenomic discoveries of Polinton-like viruses are consistent with the hypothesis that Polintons invade eukaryotic host genomes through infectious viral particles. Nematode genomes contain multiple copies of Polintons and provide an opportunity to explore the natural distribution and evolution of Polintons during this process. We performed an extensive search of Polintons across nematode genomes, identifying multiple full-length Polinton copies in several species. We provide evidence of both ancient Polinton integrations and recent mobility in strains of the same nematode species. In addition to the major nematode Polinton family, we identified a group of Polintons that are overall closely related to the major family but encode a distinct protein-primed DNA polymerase B (pPolB) that is related to homologs from a different group of Polintons present outside of the Nematoda. Phylogenetic analyses on the pPolBs support the evolutionary scenarios in which these extrinsic pPolBs that seem to derive from Polinton families present in oomycetes and molluscs replaced the canonical pPolB in subsets of Polintons found in terrestrial and marine nematodes, respectively, suggesting interphylum horizontal gene transfers. The pPolBs of the terrestrial nematode and oomycete Polintons share a unique feature, an insertion of an HNH nuclease domain, whereas the pPolBs in the marine nematode Polintons share an insertion of a VSR nuclease domain with marine mollusc pPolBs. We hypothesize that horizontal gene transfer occurs among Polintons from widely different but cohabiting hosts.

Funder

NIGMS

Long-term Postdoctoral Fellowship

Human Frontier Science Program

Bernard Cohen Postdoctoral Fellowship

Stanford Cardiovascular Institute Summer Undergraduate Fellowship

Intramural Research Program

National Institutes of Health

National Library of Medicine

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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