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Updated: Mar 15, 2026

Characterization of G Protein-coupled Receptors by a Fluorescence-based Calcium Mobilization Assay
Published on: July 28, 2014
Characterization and Expression Analysis of Receptor for Activated C Kinase from Silk-producing Insect Antheraea
Bao-Jian Zhu, Hao Yu, Sen Tian
1College of Life Sciences, Anhui Agricultural University, 130 Changjiang West Road, Hefei 230036, China. cyschx@163.com.
The receptor for activated C kinase (RACK) is involved in the immune response of the wild silkworm Antheraea pernyi. RACK gene expression increases in fat bodies after pathogen challenge, suggesting a role in innate immunity.
Area of Science:
- Insect immunology
- Molecular biology
- Biochemistry
Background:
- The receptor for activated C kinase (RACK) is a key scaffold protein regulating cellular functions.
- The specific role of RACK in the immune response of the wild silkworm Antheraea pernyi against pathogens is not well understood.
Purpose of the Study:
- To investigate the biological functions of RACK in Antheraea pernyi.
- To clone the RACK gene and analyze its expression patterns in response to immune challenges.
Main Methods:
- Gene cloning and sequence analysis of RACK.
- Recombinant protein expression and antibody production.
- SDS-PAGE, Western blot, ELISA, and real-time PCR for expression analysis.
Main Results:
- The Antheraea pernyi RACK gene sequence (1120 bp) showed high homology with insect RACK homologs.
- Recombinant RACK protein (36 kDa) was successfully expressed and an antibody was generated.
- RACK mRNA expression was highest in fat bodies and significantly induced by nucleopolyhedrovirus, E. coli, and Beauveria bassiana.
Conclusions:
- RACK is predominantly expressed in Antheraea pernyi fat bodies.
- RACK gene expression is inducible by various pathogens, indicating its potential involvement in the innate immune response of Antheraea pernyi.
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