{"title":"在 FUT1*01 等位基因背景上鉴定出一个 c.425G > A 的新型 FUT1 等位基因","authors":"Lin-Nan Shao, Yi-Cheng Yang, Chun-Xiang Li, Ning Li, Yue-Xin Xia, Shi-Hang Zhou, Xiao-Hua Liang","doi":"10.1007/s12288-024-01838-3","DOIUrl":null,"url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Background and Objectives</h3><p>The expression of the H antigen on red blood cell membranes is dependent on the human <i>FUT1</i> gene. We herein report a novel <i>FUT1</i> allele found in a Chinese individual.</p><h3 data-test=\"abstract-sub-heading\">Materials and methods</h3><p>The entire <i>FUT1</i> genes of these probands were sequenced through PacBio third-generation sequencing. 3D molecular models of the wild-type and mutant fucosyltransferases were generated using the DynaMut web-server. The effect of the mutation on the enzyme function was predicted by PROVEAN and PolyPhen2.</p><h3 data-test=\"abstract-sub-heading\">Results</h3><p>Two probands exhibited discrepancies in their ABO group typing. PacBio sequencing identified that proband 1 possessed a typical <i>ABO*B.01</i>/<i>ABO*O.01.02</i> genotype for the <i>ABO</i> gene, and was heterozygous with <i>FUT1*01</i> and a reported functionally weakened allele <i>FUT1*01W.23</i> (c.424 C > T, p.Arg142Trp) for <i>FUT1</i> gene. Proband 2 had the <i>ABO*BA.02</i>/<i>ABO*B.01</i> genotype, and was heterozygous for <i>FUT1*01.02</i> and a novel <i>FUT1*01</i>-like allele with c.425G > A (p.Arg142Gln). <i>In silico</i> analysis indicated that the c.424 C > T mutation was classified as “Deleterious” or “Damaging”, whereas the c.425G > A mutation was considered “Neutral” or “Benign”.</p><h3 data-test=\"abstract-sub-heading\">Conclusion</h3><p>We have identified a novel <i>FUT1</i> allele with c.425G > A on the <i>FUT1*01</i> allele background in an individual exhibiting the B(A) phenotype. These findings contribute to the expanding repository of knowledge regarding the H blood group system.</p>","PeriodicalId":13314,"journal":{"name":"Indian Journal of Hematology and Blood Transfusion","volume":"111 1","pages":""},"PeriodicalIF":0.9000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification of a Novel FUT1 Allele with c.425G > A on the FUT1*01 Allele Background\",\"authors\":\"Lin-Nan Shao, Yi-Cheng Yang, Chun-Xiang Li, Ning Li, Yue-Xin Xia, Shi-Hang Zhou, Xiao-Hua Liang\",\"doi\":\"10.1007/s12288-024-01838-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3 data-test=\\\"abstract-sub-heading\\\">Background and Objectives</h3><p>The expression of the H antigen on red blood cell membranes is dependent on the human <i>FUT1</i> gene. We herein report a novel <i>FUT1</i> allele found in a Chinese individual.</p><h3 data-test=\\\"abstract-sub-heading\\\">Materials and methods</h3><p>The entire <i>FUT1</i> genes of these probands were sequenced through PacBio third-generation sequencing. 3D molecular models of the wild-type and mutant fucosyltransferases were generated using the DynaMut web-server. The effect of the mutation on the enzyme function was predicted by PROVEAN and PolyPhen2.</p><h3 data-test=\\\"abstract-sub-heading\\\">Results</h3><p>Two probands exhibited discrepancies in their ABO group typing. PacBio sequencing identified that proband 1 possessed a typical <i>ABO*B.01</i>/<i>ABO*O.01.02</i> genotype for the <i>ABO</i> gene, and was heterozygous with <i>FUT1*01</i> and a reported functionally weakened allele <i>FUT1*01W.23</i> (c.424 C > T, p.Arg142Trp) for <i>FUT1</i> gene. Proband 2 had the <i>ABO*BA.02</i>/<i>ABO*B.01</i> genotype, and was heterozygous for <i>FUT1*01.02</i> and a novel <i>FUT1*01</i>-like allele with c.425G > A (p.Arg142Gln). <i>In silico</i> analysis indicated that the c.424 C > T mutation was classified as “Deleterious” or “Damaging”, whereas the c.425G > A mutation was considered “Neutral” or “Benign”.</p><h3 data-test=\\\"abstract-sub-heading\\\">Conclusion</h3><p>We have identified a novel <i>FUT1</i> allele with c.425G > A on the <i>FUT1*01</i> allele background in an individual exhibiting the B(A) phenotype. 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引用次数: 0
摘要
背景和目的红细胞膜上 H 抗原的表达依赖于人类 FUT1 基因。材料与方法通过 PacBio 第三代测序技术对这些受试者的整个 FUT1 基因进行了测序。使用 DynaMut 网络服务器生成了野生型和突变型岩藻糖基转移酶的三维分子模型。突变对酶功能的影响由 PROVEAN 和 PolyPhen2 预测。PacBio 测序结果显示,探病者 1 的 ABO 基因为典型的 ABO*B.01/ABO*O.01.02 基因型,并且是 FUT1*01 基因的杂合子,以及据报道 FUT1 基因功能减弱的等位基因 FUT1*01W.23 (c.424 C > T, p.Arg142Trp)。Proband 2 的基因型为 ABO*BA.02/ABO*B.01,是 FUT1*01.02 和一个新的 FUT1*01 样等位基因(c.425G >A(p.Arg142Gln))的杂合子。硅学分析表明,c.424 C > T 突变被归类为 "有害 "或 "损伤性 "突变,而 c.425G > A 突变被认为是 "中性 "或 "良性 "突变。这些发现有助于扩大有关 H 血型系统的知识库。
Identification of a Novel FUT1 Allele with c.425G > A on the FUT1*01 Allele Background
Background and Objectives
The expression of the H antigen on red blood cell membranes is dependent on the human FUT1 gene. We herein report a novel FUT1 allele found in a Chinese individual.
Materials and methods
The entire FUT1 genes of these probands were sequenced through PacBio third-generation sequencing. 3D molecular models of the wild-type and mutant fucosyltransferases were generated using the DynaMut web-server. The effect of the mutation on the enzyme function was predicted by PROVEAN and PolyPhen2.
Results
Two probands exhibited discrepancies in their ABO group typing. PacBio sequencing identified that proband 1 possessed a typical ABO*B.01/ABO*O.01.02 genotype for the ABO gene, and was heterozygous with FUT1*01 and a reported functionally weakened allele FUT1*01W.23 (c.424 C > T, p.Arg142Trp) for FUT1 gene. Proband 2 had the ABO*BA.02/ABO*B.01 genotype, and was heterozygous for FUT1*01.02 and a novel FUT1*01-like allele with c.425G > A (p.Arg142Gln). In silico analysis indicated that the c.424 C > T mutation was classified as “Deleterious” or “Damaging”, whereas the c.425G > A mutation was considered “Neutral” or “Benign”.
Conclusion
We have identified a novel FUT1 allele with c.425G > A on the FUT1*01 allele background in an individual exhibiting the B(A) phenotype. These findings contribute to the expanding repository of knowledge regarding the H blood group system.
期刊介绍:
Indian Journal of Hematology and Blood Transfusion is a medium for propagating and exchanging ideas within the medical community. It publishes peer-reviewed articles on a variety of aspects of clinical hematology, laboratory hematology and hemato-oncology. The journal exists to encourage scientific investigation in the study of blood in health and in disease; to promote and foster the exchange and diffusion of knowledge relating to blood and blood-forming tissues; and to provide a forum for discussion of hematological subjects on a national scale.
The Journal is the official publication of The Indian Society of Hematology & Blood Transfusion.