Bak E-J, Ishii Y, Omatsu T, Kyuwa S, Hayasaka I, Yoshikawa Y
Department of Biomedical Science, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Tokyo, Japan.
Int J Immunogenet. 2005 Jun;32(3):187-92. doi: 10.1111/j.1744-313X.2005.00506.x.
The diversity of the MHC class II region in non-human primates is a focus of biomedical research because this region plays a crucial role in the recognition of antigens in the immune system. In particular, the chimpanzee [Pan troglodytes (Patr)], which belongs to the superfamily Hominoidea, has been used as a human model for the study of diseases such as human hepatitis C virus (HCV), human hepatitis B virus (HBV) and human immunodeficiency virus (HIV) infections, to which only humans and chimpanzees are susceptible. In the present study, polymorphisms of the MHC-DPB1 gene (Patr-DPB1) in a chimpanzee colony in Japan were examined using a stepwise polymerase chain reaction (PCR) technique. In order to design a suitable primer pair which would amplify exon 2 of the Patr-DPB1 gene, a fragment of approximately 8 kb from exon 1 to exon 3 was amplified from chimpanzee genomic DNA. After designing a 500-bp primer pair at the 3' region of intron 1 and the 5' region of intron 2, analysis of DPB1 exon 2 alleles of each chimpanzee was carried out. Twenty-two chimpanzees were used in our study, and we identified seven alleles by sequence analysis on the Patr-DPB1 gene, including one new allele. The obtained nucleotide sequence patterns suggest that Patr-DPB1 alleles emerge by genetic variations such as the exchange of sequence motifs and the accumulation of point mutations.
非人类灵长类动物中MHC II类区域的多样性是生物医学研究的一个重点,因为该区域在免疫系统对抗原的识别中起着关键作用。特别是,属于类人猿超科的黑猩猩(Pan troglodytes, Patr)已被用作人类模型,用于研究人类丙型肝炎病毒(HCV)、乙型肝炎病毒(HBV)和人类免疫缺陷病毒(HIV)感染等疾病,只有人类和黑猩猩对这些疾病易感。在本研究中,使用逐步聚合酶链反应(PCR)技术检测了日本一个黑猩猩群体中MHC-DPB1基因(Patr-DPB1)的多态性。为了设计一个合适的引物对来扩增Patr-DPB1基因的外显子2,从黑猩猩基因组DNA中扩增出了一个从外显子1到外显子3的约8 kb片段。在位于内含子1的3'区域和内含子2的5'区域设计了一个500 bp的引物对后,对每只黑猩猩的DPB1外显子2等位基因进行了分析。我们的研究使用了22只黑猩猩,通过对Patr-DPB1基因的序列分析,我们鉴定出了7个等位基因,其中包括一个新等位基因。获得的核苷酸序列模式表明,Patr-DPB1等位基因是通过序列基序交换和点突变积累等遗传变异产生的。