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Survey and characterization of nonfunctional alleles of FUT2 in a database
The expression of ABO antigens in human saliva is regulated by the FUT2 gene, which encodes a secretor type α(1,2)fucosyltransferase. Secretors express ABO substrates in saliva and non-secretors do not. Secretor status is an object of concern, especially for susceptibility to various infectious dise...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862633/ https://www.ncbi.nlm.nih.gov/pubmed/33542434 http://dx.doi.org/10.1038/s41598-021-82895-w |
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author | Soejima, Mikiko Koda, Yoshiro |
author_facet | Soejima, Mikiko Koda, Yoshiro |
author_sort | Soejima, Mikiko |
collection | PubMed |
description | The expression of ABO antigens in human saliva is regulated by the FUT2 gene, which encodes a secretor type α(1,2)fucosyltransferase. Secretors express ABO substrates in saliva and non-secretors do not. Secretor status is an object of concern, especially for susceptibility to various infectious diseases. A multitude of single nucleotide polymorphisms (SNPs) and copy number variations (CNVs) have been reported, and they show unique distributions among different populations. In this study, we selected 18 uncharacterized FUT2 alleles listed in the Erythrogene database and obtained genomic DNA having these alleles. We experimentally confirmed the haplotypes, but 10 of 18 alleles disagreed with those in the database, which may be attributed to their low frequency. We then examined the activity of the encoded α(1,2)fucosyltransferase for 13 alleles by flow cytometry of H antigen expression. The impact of each nonsynonymous SNP on the enzyme was also estimated by software. We finally identified two non-secretor alleles (se(610)and se(357,856,863)) and one weak secretor allele (se(262,357)), while in silico analysis predicted that many alleles impair the function. The present results suggest that correct haplotyping and functional assays are desirable for analysis of the FUT2 gene. |
format | Online Article Text |
id | pubmed-7862633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78626332021-02-08 Survey and characterization of nonfunctional alleles of FUT2 in a database Soejima, Mikiko Koda, Yoshiro Sci Rep Article The expression of ABO antigens in human saliva is regulated by the FUT2 gene, which encodes a secretor type α(1,2)fucosyltransferase. Secretors express ABO substrates in saliva and non-secretors do not. Secretor status is an object of concern, especially for susceptibility to various infectious diseases. A multitude of single nucleotide polymorphisms (SNPs) and copy number variations (CNVs) have been reported, and they show unique distributions among different populations. In this study, we selected 18 uncharacterized FUT2 alleles listed in the Erythrogene database and obtained genomic DNA having these alleles. We experimentally confirmed the haplotypes, but 10 of 18 alleles disagreed with those in the database, which may be attributed to their low frequency. We then examined the activity of the encoded α(1,2)fucosyltransferase for 13 alleles by flow cytometry of H antigen expression. The impact of each nonsynonymous SNP on the enzyme was also estimated by software. We finally identified two non-secretor alleles (se(610)and se(357,856,863)) and one weak secretor allele (se(262,357)), while in silico analysis predicted that many alleles impair the function. The present results suggest that correct haplotyping and functional assays are desirable for analysis of the FUT2 gene. Nature Publishing Group UK 2021-02-04 /pmc/articles/PMC7862633/ /pubmed/33542434 http://dx.doi.org/10.1038/s41598-021-82895-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Soejima, Mikiko Koda, Yoshiro Survey and characterization of nonfunctional alleles of FUT2 in a database |
title | Survey and characterization of nonfunctional alleles of FUT2 in a database |
title_full | Survey and characterization of nonfunctional alleles of FUT2 in a database |
title_fullStr | Survey and characterization of nonfunctional alleles of FUT2 in a database |
title_full_unstemmed | Survey and characterization of nonfunctional alleles of FUT2 in a database |
title_short | Survey and characterization of nonfunctional alleles of FUT2 in a database |
title_sort | survey and characterization of nonfunctional alleles of fut2 in a database |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862633/ https://www.ncbi.nlm.nih.gov/pubmed/33542434 http://dx.doi.org/10.1038/s41598-021-82895-w |
work_keys_str_mv | AT soejimamikiko surveyandcharacterizationofnonfunctionalallelesoffut2inadatabase AT kodayoshiro surveyandcharacterizationofnonfunctionalallelesoffut2inadatabase |