Mosquitoes Possess Specialized Cuticular Proteins That Are Evolutionarily Related to the Elastic Protein Resilin

Author:

Ohkubo Sakura1,Shintaku Tohki1,Mine Shotaro12,Yamamoto Daisuke S.3ORCID,Togawa Toru1ORCID

Affiliation:

1. Department of Biosciences, College of Humanities and Sciences, Nihon University, Sakurajyosui 3-25-40, Setagaya-ku, Tokyo 156-8550, Japan

2. Division of Insect Advanced Technology, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Owashi 1-2, Tsukuba 305-8634, Japan

3. Division of Medical Zoology, Department of Infection and Immunity, Jichi Medical University, Yakushiji 3311-1, Shimotsuke 329-0498, Japan

Abstract

Resilin is an elastic protein that is vital to insects’ vigorous movement. Canonical resilin proteins possess the R&R Consensus, a chitin-binding domain conserved in a family of cuticular proteins, and highly repetitive sequences conferring elastic properties. In the malaria vector mosquito, Anopheles gambiae, however, a cuticular protein has been found that has an R&R Consensus resembling that of resilin but lacks the repetitive sequences (here, we call it resilin-related or resilin-r). The relationship between resilin-r and resilin was unclear. It was also unknown whether resilin-r is conserved in mosquitoes. In this paper, phylogenetic and structural analyses were performed to reveal the relationship of resilin homologous proteins from holometabolous insects. Their chitin-binding abilities were also assessed. A resilin-r was found in each mosquito species, and these proteins constitute a clade with resilin from other insects based on the R&R Consensus sequences, indicating an evolutionary relationship between resilin-r and resilin. The resilin-r showed chitin-binding activity as same as resilin, but had distinct structural features from resilin, suggesting that it plays specialized roles in the mosquito cuticle. Another resilin-like protein was found to exist in each holometabolous insect that possesses resilin-like repetitive sequences but lacks the R&R Consensus. These results suggest that similar evolutionary events occurred to create resilin-r and resilin-like proteins.

Funder

JSPS KAKENHI

Individual Research Expense of the College of Humanities and Sciences at Nihon University, and the Research Grant of Institute of Natural Science at Nihon University

Publisher

MDPI AG

Subject

Insect Science

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