کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2815914 1159901 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Molecular cloning and characterization of a novel bovine IFN-ε
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
پیش نمایش صفحه اول مقاله
Molecular cloning and characterization of a novel bovine IFN-ε
چکیده انگلیسی


• Bovine IFN-ε was first cloned here and the characterization of bovine IFN-ε was analyzed.
• The mature peptide was highly expressed in prokaryotic expression system, and it could be overexpressed in MDBK cells.
• Bovine IFN-ε has moderate antiviral activity on MDBK, BT, EBK and PK-15 cells, but not on BHK-21 and MDCK cells.
• Bovine IFN-ε gene can be constitutively expressed in the liver, thymus, kidney, small intestine and testis.

A bovine IFN-ε (BoIFN-ε) gene was amplified from bovine liver genomic DNA consisting of a 463 bp partial 5′UTR, 582 bp complete ORF and 171 bp partial 3′UTR, which encodes a protein of 193 amino acids with a 21-amino acid signal peptide and shares 61 to 87% identity with other species IFN-ε. Then BoIFN-ε gene was characterized, and it can be transcribed in EBK cells at a high level after being infected by VSV. Recombinant proteins were expressed in Escherichia coli and the antiviral activity was determined in vitro, which revealed that bovine IFN-ε has less antiviral activity than bovine IFN-α. In addition, an immunofluorescence assay indicated that BoIFN-ε expressed in MDBK cells could be detected by polyclonal antibody against BoIFN-ε. Furthermore, the BoIFN-ε gene can be constitutively expressed in the liver, thymus, kidney, small intestine and testis, but not in the heart. This study revealed that BoIFN-ε has the typical characteristics of type I interferon and can be expressed constitutively in certain tissue, which not only can be a likely candidate for a novel, effective therapeutic agent, but also facilitate further research on the role of bovine IFN system.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 558, Issue 1, 1 March 2015, Pages 25–30
نویسندگان
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