等位基因
遗传学
打字
生物
寡核苷酸
HLA-A
人类白细胞抗原
低聚物限制
多态性(计算机科学)
HLA-B
序列(生物学)
分子生物学
基因
抗原
作者
Yunlei He,W. Wang,Zhijie Han,J. He,N.‐Y. Chen,Lina Dong,Sudan Tao,W. Zhang,J. He,Faming Zhu,H.‐J. Lv
摘要
Summary Currently, Luminex technology based on the PCR sequence‐specific oligonucleotide (SSO) probe method has been widely used for HLA genotyping in the immunogenetics laboratories. Here, we reported a case with HLA‐B allele dropout by Luminex technology. The initial HLA‐B result of the Luminex method with a commercial agent kit was inconclusive, and then, the result of PCR‐SBT technology indicated the dropout as a HLA‐B*58 allele. Subsequently, the full‐length sequence of HLA‐B allele was determined by TOPO‐TA cloning, and a novel allele B*58:01:01:02 was identified in the individual. Compared with HLA‐B*58:01:01:01, the novel allele showed some nucleotides difference at 509 C>T, 521 T>G and CCC insertion in position 503 of intron 2. According to the full‐length sequence, the new mutations of intron 2 were contributed to HLA‐B locus allele dropout in the sample. Our results indicated multiplatform should be used to improve the HLA typing accuracy when a conclusive HLA genotype cannot be determined.
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