Alizadeh M, Legras C, Semana G, Le Bouteiller P, Genetet B, Fauchet R
Histocompatibility Laboratory, Regional Center for Blood Transfusion, Rennes, France.
Hum Immunol. 1993 Nov;38(3):206-12. doi: 10.1016/0198-8859(93)90542-9.
HLA-G gene polymorphism was analyzed by RFLP using seven restriction enzymes and an HLA-G locus-specific probe. Hybridization of 55 DNAs digested with three enzymes (Taq I, Pst I, and Bgl II) revealed two polymorphic bands in each case. RFLP patterns obtained with Taq I and Pst I corresponded to the same allelic polymorphism and differed from the Bgl II polymorphism. Combining both polymorphisms enabled determination of four alleles. Allelic frequencies were calculated: 40% of the subjects tested had allele 1, 36% had allele 2, 22% had allele 3, and 2% had allele 4. Analyzing the complete HLA class I phenotype revealed strong linkage disequilibrium with the HLA-A locus. The polymorphism described is located in the 3' flanking region of the gene. Moreover, extended HLA-A haplotypes were constructed by combining the HLA-G polymorphism with other class-I-sequence polymorphisms.
使用七种限制性内切酶和一个HLA - G基因座特异性探针,通过限制性片段长度多态性(RFLP)分析HLA - G基因多态性。用三种酶(Taq I、Pst I和Bgl II)消化的55个DNA进行杂交,在每种情况下均显示出两条多态性条带。用Taq I和Pst I获得的RFLP模式对应于相同的等位基因多态性,与Bgl II多态性不同。结合这两种多态性能够确定四个等位基因。计算等位基因频率:40%的受试对象有等位基因1,36%有等位基因2,22%有等位基因3,2%有等位基因4。分析完整的HLA I类表型显示与HLA - A基因座存在强连锁不平衡。所描述的多态性位于该基因的3'侧翼区域。此外,通过将HLA - G多态性与其他I类序列多态性相结合构建了扩展的HLA - A单倍型。