FOXP3 is a transcription factor predominantly expressed in CD4(+) CD25(+) thymocytes and CD4(+) CD25(+) peripheral T cells. It has been reported that variation in the FOXP3 gene (FOXP3) could cause impaired immune regulation. Using PCR-SSCP, variation in exon 4, exon 9-10 and exon 13-14 of ovine FOXP3, covering three functional domains (a proline rich domain, a leucine zipper-like motif and the forkhead domain, respectively) was investigated. Four SSCP banding patterns were observed for the exon 13-14 amplicon, while no variation was detected in either exon 4 or exon 9-10. Either one or two SSCP banding patterns were observed in the sheep studied. In accordance with the X chromosome location of FOXP3, ewes were homozygous or heterozygous, while rams were hemizygous. Sequencing of DNA corresponding to the four PCR-SSCP patterns for exon 13-14, revealed four unique DNA sequences which resulted from both sequence and length variation. These comprised of two SNPs (one in intron 13 and the other in exon 14), and variation in copy number for a hexa-nucleotide repeat (TGGCCC)(n) in intron 13. These results indicate that ovine FOXP3 is polymorphic and the variation detected in this region may have implications for immune regulation in sheep. (C) 2011 Elsevier B.V. All rights reserved.
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Univ British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
BC Childrens Hosp, Res Inst, Vancouver, BC, CanadaUniv British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
Pesenacker, Anne M.
Cook, Laura
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Univ British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
BC Childrens Hosp, Res Inst, Vancouver, BC, CanadaUniv British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
Cook, Laura
Levings, Megan K.
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Univ British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
BC Childrens Hosp, Res Inst, Vancouver, BC, CanadaUniv British Columbia, Dept Surg, Vancouver, BC V5Z 1M9, Canada
机构:
Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute
Yan-hui Chen
Heng-hui Zhang
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Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute
Heng-hui Zhang
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Yan Wang
Xing-wang Xie
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Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute
Xing-wang Xie
Ran Fei
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Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute
Ran Fei
Xue-yan Wang
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Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute
Xue-yan Wang
Lai Wei
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Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute
Lai Wei
Hong-song Chen
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Peking University People’s Hospital,Peking University Hepatology Institute
Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver DiseasesPeking University People’s Hospital,Peking University Hepatology Institute