A small heat shock protein 21 (sHSP21) mediates immune responses in Chinese oak silkworm Antheraea pernyi

被引:27
作者
Liu, Qiu-Ning [1 ]
Liu, Yu [1 ,2 ]
Xin, Zhao-Zhe [1 ,2 ]
Zhu, Xiao-Yu [1 ]
Ge, Bao-Ming [1 ]
Li, Chao-Feng [1 ]
Wang, Dong [1 ]
Bian, Xun-Guang [1 ]
Yang, Li [1 ]
Chen, Li [3 ]
Tian, Ji-Wu [4 ]
Zhou, Chun-Lin [1 ]
Tang, Bo-Ping [1 ]
机构
[1] Yancheng Teachers Univ, Sch Ocean & Biol Engn, Jiangsu Synthet Innovat Ctr Coastal Bioagr,Jiangs, Jiangsu Prov Key Lab Coastal Wetland Bioresources, 50 Kaifang Ave, Yancheng 224051, Jiangsu, Peoples R China
[2] Nanjing Univ Technol, Coll Biotechnol & Pharmaceut Engn, Nanjing 210009, Jiangsu, Peoples R China
[3] Henan Inst Sericultural Sci, Zhengzhou 450002, Henan, Peoples R China
[4] Agr Dept Henan Prov, Zhengzhou 450002, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Antheraea pernyi; Small heat shock protein 21; Expression analysis; DIFFERENTIALLY EXPRESSED GENES; MOLECULAR-CLONING; LEPIDOPTERA SATURNIIDAE; DROSOPHILA-MELANOGASTER; STRESS; IDENTIFICATION; DIAPAUSE; L;
D O I
10.1016/j.ijbiomac.2018.01.147
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small heat shock proteins (sHSPs) are conserved among insects and play an important role in the regulation of many biological processes, including temperature stress, abiotic stress, immune responses, metamorphosis, and embryo development. Antheraea pernyi is an economically valuable silk-producing moth and source of insect food containing high-quality protein. The aim of this study was to quantify expression of the ApsHSP21 gene in response to pathogen-associated molecular patterns (PAMPs) and nucleopolyhedrovirus (NPV) challenge. The deduced ApsHSP21 protein sequence consists of 186 residues with a calculated molecular mass of 21.0 kDa and an isoelectronic point (pI) of 6.63. The protein contains a conserved alpha-crystallin domain (ACD), and includes two casein kinase II phosphorylation sites, a protein kinase C phosphorylation site, two tyrosine kinase phosphorylation sites, and various polypeptide binding sites. Phylogenetic analysis revealed that ApsHSP21 is closely related to homologs from other insects. Real-time quantitative reverse transcription PCR (qRT-PCR) analysis revealed that expression of ApsHSP21 was significantly up-regulated at different timepoints following simulated pathogen challenge with lipopolysaccharide (LPS), peptidoglycan (PGN), glucan, and NPV. The results suggest sHSP21 is involved in innate immune responses in A. pernyi. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1027 / 1031
页数:5
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