Cloning and Functional Characterization of a Novel [beta]-GRP Gene From Melanotus cribricollis

In this study, a novel [beta]-1,3-glucan recognition protein gene ([beta]-GRP) was identified from Melanotus cribricollis, and its potential role in the immune response was investigated. The full length of [beta]-GRP cDNA (Accession Number: MT941530) was 1644 bp, encoding a protein composed of 428 a...

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Veröffentlicht in:Journal of insect science (Tucson, Ariz.) Ariz.), 2022-09, Vol.22 (5)
Hauptverfasser: Ye, Bihuan, Song, Qiyan, Li, Haibo, Shen, Jianjun, Wu, Chenyou, Shu, Jinping, Zhang, Yabo
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container_title Journal of insect science (Tucson, Ariz.)
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creator Ye, Bihuan
Song, Qiyan
Li, Haibo
Shen, Jianjun
Wu, Chenyou
Shu, Jinping
Zhang, Yabo
description In this study, a novel [beta]-1,3-glucan recognition protein gene ([beta]-GRP) was identified from Melanotus cribricollis, and its potential role in the immune response was investigated. The full length of [beta]-GRP cDNA (Accession Number: MT941530) was 1644 bp, encoding a protein composed of 428 amino acids. The theoretical molecular weight and the isoelectric point were 51.53 kDa and 6.17, respectively. The amino acid sequence of [beta]-GRP from M. cribricollis was closely related to that of. [beta]-GRP-like from Photinus pyralis, and was predicted to contain conserved GH16 domain without glucanase active site. The results of real-time quantitative PCR showed that fungal infection of Metarhizium pingshaense may significantly upregulated the expression level of [beta]-GRP gene. The RNAi suppression of [beta]-GRP gene expression significantly increased the corrected cumulative mortality. Meanwhile, antimicrobial peptide genes defensin and lysozyme were significantly downregulated after interference of p-GRRTaken together, these results suggest that [beta]-GRP of M. cribricollis probably participates in the host immune system by mediating the expression of antimicrobial peptides. This study provides comprehensive insights into the innate immune system of insect larvae.
doi_str_mv 10.1093/jisesa/ieac051
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The full length of [beta]-GRP cDNA (Accession Number: MT941530) was 1644 bp, encoding a protein composed of 428 amino acids. The theoretical molecular weight and the isoelectric point were 51.53 kDa and 6.17, respectively. The amino acid sequence of [beta]-GRP from M. cribricollis was closely related to that of. [beta]-GRP-like from Photinus pyralis, and was predicted to contain conserved GH16 domain without glucanase active site. The results of real-time quantitative PCR showed that fungal infection of Metarhizium pingshaense may significantly upregulated the expression level of [beta]-GRP gene. The RNAi suppression of [beta]-GRP gene expression significantly increased the corrected cumulative mortality. Meanwhile, antimicrobial peptide genes defensin and lysozyme were significantly downregulated after interference of p-GRRTaken together, these results suggest that [beta]-GRP of M. cribricollis probably participates in the host immune system by mediating the expression of antimicrobial peptides. 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Meanwhile, antimicrobial peptide genes defensin and lysozyme were significantly downregulated after interference of p-GRRTaken together, these results suggest that [beta]-GRP of M. cribricollis probably participates in the host immune system by mediating the expression of antimicrobial peptides. 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source Oxford Journals Open Access Collection; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Amino acids
Cloning
Gene expression
Genes
Genetic aspects
Health aspects
Immune response
Infection
Lysozyme
Peptides
Protection and preservation
Zoological research
title Cloning and Functional Characterization of a Novel [beta]-GRP Gene From Melanotus cribricollis
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