Innate immunity evolution in underrepresented metazoans and the implications when opting for similarity-metrics vs hidden Markov models


Meeting Abstract

67-3  Sunday, Jan. 5 14:00 – 14:15  Innate immunity evolution in underrepresented metazoans and the implications when opting for similarity-metrics vs. hidden Markov models TASSIA, MG*; DAVID, KT; HALANYCH, KM; Auburn University, Auburn, AL; Auburn University, Auburn, AL; Auburn University, Auburn, AL mgt0007@auburn.edu

In this study, we investigate the evolution of innate immunity signaling components among hemichordates and other underrepresented, and/or non-model, metazoans using a hidden Markov model (HMM)-based approach. Previous studies have shown that although the core innate immunity signaling pathways possess deep roots within Metazoa, the receptors responsible for host-pathogen interfacing exhibit dynamic diversification events within several bilaterian lineages such as annelids, bivalves, and echinoids. Like many signaling pathways, innate immunity-associated proteins fundamentally rely on domains of discrete characteristics – such as hydrophobic ligand binding, transmembrane helices, or catabolic activity. The identification and classification of any given protein’s domain architecture is integral for inferring functional conservation/diversification among related proteins, particularly when investigating understudied, non-model taxa. In this study, we investigate three vital innate immunity protein families: Toll-like receptors, NOD-like receptors, and RIG-1-like receptors. The bioinformatic pipeline established here also principally addresses issues raised by database bias towards classic biomedical model systems (e.g., mouse, fly, and human). We show that HMM-based approaches, such as the one used in this study, provide a powerful alternative to similarity-based searches (e.g., BLAST); furthermore, the pipeline developed here can be applied to a large variety of protein families and taxa dependent upon the user’s target protein and phylogenetic depth.

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