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Molecular characterization of Antheraea mylitta arylphorin gene and its encoded protein.
Dutta, Soumita; Mohapatra, Jugal; Ghosh, Ananta Kumar.
Afiliación
  • Dutta S; Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, 721302, West Bengal, India.
  • Mohapatra J; Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, 721302, West Bengal, India.
  • Ghosh AK; Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, 721302, West Bengal, India. Electronic address: aghosh@bt.iitkgp.ac.in.
Arch Biochem Biophys ; 692: 108540, 2020 10 15.
Article en En | MEDLINE | ID: mdl-32783895
Antheraea mylitta arylphorin protein was extracted from the silk gland of fifth instar larvae and purified by ammonium sulphate precipitation, ion-exchange, and gel filtration chromatography. The N-terminal sequencing of ten amino acids (NH2-SVVHPPHHEV-COOH) showed similarity with Antheraea pernyi arylphorin. Based on N-terminal and C-terminal A. pernyi arylphorin sequences, primers were designed, and A. mylitta arylphorin cDNA was cloned by RT-PCR from silk gland mRNA. Sequencing of complete cDNA including 25 nucleotides at 5' UTR (obtained by 5' RACE) showed that it consisted of an ORF of 2115 nucleotides which could encode a protein of 704 amino acids (predominantly aromatic residues) having molecular weight 83 kDa. Homology modelling was done using A. pernyi arylphorin as a template. Cloned arylphorin cDNA was expressed in E. coli and recombinant His-tagged protein was purified by Ni-NTA affinity chromatography. Analysis of tissue-specific expression of arylphorin by real-time PCR showed maximum expression in the fat body followed by silk gland and integument. 5' flanking region (759 bp) of arylphorin gene was amplified by inverse PCR and the full length gene (5359 nucleotides) containing five exons and four introns was cloned from the A. mylitta genomic DNA and sequenced. Polyclonal antibody was raised against purified arylphorin and more native arylphorin protein (500 kDa) was purified from the fat body by antibody affinity chromatography. Study of mitogenic effect of native and chymotrypsin hydrolysate of arylphorin on different insect cell lines showed that arylphorin could be used as serum substitute for in vitro cultivation of insect cells.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cuerpo Adiposo / Regulación de la Expresión Génica / Genes de Insecto / Proteínas de Insectos / Regiones no Traducidas 5' / Mariposas Nocturnas Límite: Animals Idioma: En Revista: Arch Biochem Biophys Año: 2020 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cuerpo Adiposo / Regulación de la Expresión Génica / Genes de Insecto / Proteínas de Insectos / Regiones no Traducidas 5' / Mariposas Nocturnas Límite: Animals Idioma: En Revista: Arch Biochem Biophys Año: 2020 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos