期刊
JOURNAL OF GENERAL VIROLOGY
卷 89, 期 -, 页码 2447-2455出版社
SOC GENERAL MICROBIOLOGY
DOI: 10.1099/vir.0.2008/001743-0
关键词
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资金
- Biotechnology and Biological Sciences Research Council
- Scottish Executive Environment
- Regional Affairs Department
- Swiss National Science foundation [3100A0-12498]
- Royal Society (London) University Research Fellowship
- Biotechnology and Biological Sciences Research Council [BBS/B/00468] Funding Source: researchfish
- Medical Research Council [MC_U130169960] Funding Source: researchfish
- MRC [MC_U130169960] Funding Source: UKRI
We have characterized a novel, captured and fully functional viral interleukin (IL)-10 homologue (OvHVIL-10) from the gammaherpesvirus ovine herpesvirus 2. Unlike IL-10 homologues from other gammaherpesviruses, the OvHVIL-10 peptide sequence was highly divergent from that of the host species. The OvHVIL-10 gene is unique amongst virus captured genes in that it has precisely retained the original cellular exon structure, having five exons; of similar sizes to the cellular counterparts. However, the sizes of the introns are dramatically reduced. The OvHVIL-10 protein was shown to be a non-glycosylated, secreted protein of M-r 21 000 with a signal peptidase cleavage site between amino acids 26 and 27 of the nascent peptide. Functional assays showed that OvHVIL-10, in a similar way to ovine IL-10, stimulated mast cell proliferation and inhibited macrophage inflammatory chemokine production. This is the first example of a captured herpesvirus gene retaining the full cellular gene structure.
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