4.7 Review

The Natterin Proteins Diversity: A Review on Phylogeny, Structure, and Immune Function

Journal

TOXINS
Volume 13, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/toxins13080538

Keywords

Thalassophryne nattereri; Natterin; aerolysin; protein evolution; immune function; bioinformatics

Funding

  1. Sao Paulo Research Foundation-FAPESP [2013/07467-1, 2019/27677-7, 2019/02333-3]
  2. National Council for Scientific and Technological Development-CNPq [305414/2019-4]
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior-Brazil (CAPES) [001]

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By conducting a thorough screening of genome databases across a wide range of species, researchers have identified new sequences and expanded the number of members within the Natterin protein group. The survey revealed 331 species with Natterin-like proteins, primarily found in fish, with insects and birds being the groups with the most species included in the analysis. Detailed annotations provided insights into the conserved motifs and functional roles of these proteins in the innate immune defense system of hosts.
Since the first record of the five founder members of the group of Natterin proteins in the venom of the medically significant fish Thalassophryne nattereri, new sequences have been identified in other species. In this work, we performed a detailed screening using available genome databases across a wide range of species to identify sequence members of the Natterin group, sequence similarities, conserved domains, and evolutionary relationships. The high-throughput tools have enabled us to dramatically expand the number of members within this group of proteins, which has a remote origin (around 400 million years ago) and is spread across Eukarya organisms, even in plants and primitive Agnathans jawless fish. Overall, the survey resulted in 331 species presenting Natterin-like proteins, mainly fish, and 859 putative genes. Besides fish, the groups with more species included in our analysis were insects and birds. The number and variety of annotations increased the knowledge of the obtained sequences in detail, such as the conserved motif AGIP in the pore-forming loop involved in the transmembrane barrel insertion, allowing us to classify them as important constituents of the innate immune defense system as effector molecules activating immune cells by interacting with conserved intracellular signaling mechanisms in the hosts.

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