[Analysis of a Chinese pedigree with Bw subtype due to a novel variant of α-1,3-N-acetylgalactosaminyltransferase gene].

Wen Wu, Xinping Zhang, Chao Liu, Xiangyan Huang
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Abstract

Objective: To explore the serological characteristics and genetic variant in a Chinese pedigree with Bw subtype.

Methods: A 32-year-old female proband who had undergone prenatal examination on December 10, 2020 at the 960th Hospital of the PLA Joint Logistics Support Force and five members from her pedigree were selected as the study subjects. Peripheral blood samples were collected and subjected to ABO blood group phenotyping with serological methods and ABO blood group genotyping with fluorescent PCR. Genetic testing and haplotype analysis were carried out by direct sequencing of the entire coding region of the ABO gene in the proband and cloned sequencing of exons 1-7.

Results: The blood type serology of the proband showed Bw, and her ABO blood type genotype determined by fluorescence PCR was B/O. The direct sequencing results showed that the proband had matched the ABO*O.01.01/ABO*B.01 genotype and carried a c.1A>G variant. Cloned sequencing has confirmed the c.1A>G variant to have occurred in the ABO*B.01 allele. Family analysis revealed that the mother of the proband had an O blood type, her husband had a B phenotype, and her three children had a normal B blood type. DNA sequencing showed that the two sons of the proband had a genotype of ABO*B.01 and c.1A>G/ABO*B.01. The daughter of the proband was ABO*O.01.01/ABO*B.01, whilst her mother was ABO*O.01.01/ABO *O.01.02. The novel c.1A>G variant sequence has been registered with the database with a number MZ076785 1.

Conclusion: The novel c.1A>G variant of exon 1 of α- 1,3 galactose aminotransferase gene probably underlay the reduced expression of B antigen in this pedigree.

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[α-1,3-N-乙酰半乳糖氨基转移酶基因新型变异导致的 Bw 亚型中国血统分析]。
摘要方法:选取 2020 年 12 月 10 日在中国人民解放军总后勤部第 960 医院接受产前检查的一名 32 岁女患者及其血统中的五名成员作为研究对象,探讨 Bw 亚型中国血统的血清学特征和遗传变异:方法:选取 2020 年 12 月 10 日在中国人民解放军联合后勤保障部队第 960 医院接受产前检查的一名 32 岁女性原发性 Bw 亚型患者及其血亲中的 5 名成员作为研究对象。采集外周血样本,用血清学方法进行 ABO 血型表型分析,用荧光 PCR 方法进行 ABO 血型基因分型分析。基因检测和单倍型分析是通过直接测序 proband 的 ABO 基因整个编码区和克隆测序外显子 1-7 来进行的:结果:疑似患者的血型血清学检查结果为 Bw,荧光 PCR 测定的 ABO 血型基因型为 B/O。直接测序结果显示,该患者符合 ABO*O.01.01/ABO*B.01 基因型,并携带 c.1A>G 变异。克隆测序证实,c.1A>G 变异发生在 ABO*B.01 等位基因中。家庭分析表明,病例母亲的血型为 O 型,其丈夫的血型为 B 型,三个孩子的血型均为正常的 B 型。DNA 测序显示,病例的两个儿子的基因型为 ABO*B.01 和 c.1A>G/ABO*B.01。原告的女儿是 ABO*O.01.01/ABO*B.01 血型,而她的母亲是 ABO*O.01.01/ABO *O.01.02。新型 c.1A>G 变异序列已在数据库中登记,编号为 MZ076785 1.Conclusion:结论:α- 1,3 半乳糖氨基转移酶基因第 1 外显子的新型 c.1A>G 变异可能是该血统中 B 抗原表达降低的基础。
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来源期刊
中华医学遗传学杂志
中华医学遗传学杂志 Medicine-Medicine (all)
CiteScore
0.50
自引率
0.00%
发文量
9521
期刊介绍: Chinese Journal of Medical Genetics is a medical journal, founded in 1984, under the supervision of the China Association for Science and Technology, sponsored by the Chinese Medical Association (hosted by Sichuan University), and is now a monthly magazine, which attaches importance to academic orientation, adheres to the scientific, scholarly, advanced, and innovative, and has a certain degree of influence in the industry. Chinese Journal of Medical Genetics is a journal of Peking University, and is now included in Peking University Journal (Chinese Journal of Humanities and Social Sciences), CSCD Source Journals of Chinese Science Citation Database (with extended version), Statistical Source Journals (China Science and Technology Dissertation Outstanding Journals), Zhi.com (in Chinese), Wipu (in Chinese), Wanfang (in Chinese), CA Chemical Abstracts (U.S.), JST (Japan Science and Technology Science and Technology), and JST (Japan Science and Technology Science and Technology Research Center). ), JST (Japan Science and Technology Agency), Pж (AJ) Abstracts Journal (Russia), Copernicus Index (Poland), Cambridge Scientific Abstracts, Abstracts and Citation Database, Abstracts Magazine, Medical Abstracts, and so on.
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