Abstract

Prokaryote mobilome genomes rely on host machineries for survival and replication. Given that mobile genetic elements (MGEs) derive their energy from host cells, we investigated the diversity of ATP-utilizing proteins in MGE genomes to determine whether they might be associated with proteins that could suppress related host proteins that consume energy. A comprehensive search of 353 huge phage genomes revealed that up to 9% of the proteins have ATPase domains. For example, ATPase proteins constitute ∼3% of the genomes of Lak phages with ∼550 kbp genomes that occur in the microbiomes of humans and other animals. Statistical analysis shows the number of ATPase proteins increases linearly with genome length, consistent with a large sink for host ATP during replication of megaphages. Using metagenomic data from diverse environments, we found 505 mobilome proteins with ATPase domains fused to diverse functional domains. Among these composite ATPase proteins, 61.6% have known functional domains that could contribute to host energy diversion during the mobilome infection cycle. As many have domains that are known to interact with nucleic acids and proteins, we infer that numerous ATPase proteins are used during replication and for protection from host immune systems. We found a set of uncharacterized ATPase proteins with nuclease and protease activities, displaying unique domain architectures that are energy intensive based on the presence of multiple ATPase domains. In many cases, these composite ATPase proteins genomically co-localize with small proteins in genomic contexts that are reminiscent of toxin-antitoxin systems and phage helicase-antibacterial helicase systems. Small proteins that function as inhibitors may be a common strategy for control of cellular processes, thus could inspire future biochemical experiments for the development of new nucleic acid and protein manipulation tools, with diverse biotechnological applications.

Highlights

  • The mobilome in prokaryotes includes plasmids, bacteriophages, viruses of archaea and transposons that can move between host genomes

  • Given that mobile genetic elements (MGEs) derive their energy from host cells, we investigated the diversity of ATP-utilizing proteins in MGE genomes to determine whether they might be associated with proteins that could suppress related host proteins that consume energy

  • As the phage genome size varies from 104 kbp to 735 kbp, the number of ATPase proteins was plotted against the genome size (Supplementary Figure 1A)

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Summary

Introduction

The mobilome in prokaryotes includes plasmids, bacteriophages (phages), viruses of archaea and transposons that can move between host genomes. These mobile genetic elements are dependent on host machineries for transcription and replication (Frost et al, 2005; Gogarten and Townsend, 2005; Thomas and Nielsen, 2005). This parasitic propagation strategy necessitates the diversion of host energy, as these mobile genetic elements lack energy generating machinery (e.g., ATP synthase) and structures (e.g., the cell membrane). These intra-genomic conflicts between hosts and mobilomes constitute a huge ATP sink

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