Abstract

Annexins are Ca2+-binding, membrane-interacting proteins, widespread among eukaryotes, consisting usually of four structurally similar repeated domains. It is accepted that vertebrate annexins derive from a double genome duplication event. It has been postulated that a single domain annexin, if found, might represent a molecule related to the hypothetical ancestral annexin. The recent discovery of a single-domain annexin in a bacterium, Cytophaga hutchinsonii, apparently confirmed this hypothesis. Here, we present a more complex picture. Using remote sequence similarity detection tools, a survey of bacterial genomes was performed in search of annexin-like proteins. In total, we identified about thirty annexin homologues, including single-domain and multi-domain annexins, in seventeen bacterial species. The thorough search yielded, besides the known annexin homologue from C. hutchinsonii, homologues from the Bacteroidetes/Chlorobi phylum, from Gemmatimonadetes, from beta- and delta-Proteobacteria, and from Actinobacteria. The sequences of bacterial annexins exhibited remote but statistically significant similarity to sequence profiles built of the eukaryotic ones. Some bacterial annexins are equipped with additional, different domains, for example those characteristic for toxins. The variation in bacterial annexin sequences, much wider than that observed in eukaryotes, and different domain architectures suggest that annexins found in bacteria may actually descend from an ancestral bacterial annexin, from which eukaryotic annexins also originate. The hypothesis of an ancient origin of bacterial annexins has to be reconciled with the fact that remarkably few bacterial strains possess annexin genes compared to the thousands of known bacterial genomes and with the patchy, anomalous phylogenetic distribution of bacterial annexins. Thus, a massive annexin gene loss in several bacterial lineages or very divergent evolution would appear a likely explanation. Alternative evolutionary scenarios, involving horizontal gene transfer between bacteria and protozoan eukaryotes, in either direction, appear much less likely. Altogether, current evidence does not allow unequivocal judgement as to the origin of bacterial annexins.

Highlights

  • As of January 19th, 2013, 12795 PubMed articles mention annexins in the title or abstract, making them one of the well studied protein families

  • Annexins have been described as eukaryote-specific proteins, a single domain annexin protein has been reported in a bacterium of the Bacteroidetes/Chlorobi phylum, Cytophaga hutchinsonii [14]

  • This has prompted us to explore protein sequence databases in search of more bacterial annexin homologues

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Summary

Introduction

As of January 19th, 2013, 12795 PubMed articles mention annexins in the title or abstract, making them one of the well studied protein families. Annexins are a multi-functional protein family, widespread in eukaryotes. The four domains usually share 40– 50% sequence identity, some studies reveal that domain III is more divergent than the other domains, suggesting that the other domains might have arisen from a monomeric domain III by gene duplications [2,3,4]. The diverse biological functions of annexins include regulation of membrane trafficking and calcium homeostasis, actin and integrin binding, ATPase, GTPase, and peroxidase activity [7,8,9,10]. Gene duplications at different periods during eukaryotic evolution have contributed to the diversity in the annexin sequence, structure and function [11,12]

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