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Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay
Human protection of telomeres 1 (POT1) gene is a single stranded telomere binding proteins with a critical role in ensuring chromosome stability. There have been variants of POT1 gene, and the polymorphisms of POT1 gene were associated with some diseases. Polymerase chain reaction–restriction fragme...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864762/ https://www.ncbi.nlm.nih.gov/pubmed/27247888 http://dx.doi.org/10.1186/s40064-016-2214-5 |
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author | Wang, Sihua Duan, Xiaoran Wang, Tuanwei Feng, Xiaolei Wang, Pengpeng Yao, Wu Wu, Yongjun Wu, Yiming Yan, Zhen Feng, Feifei Yu, Songcheng Wang, Wei |
author_facet | Wang, Sihua Duan, Xiaoran Wang, Tuanwei Feng, Xiaolei Wang, Pengpeng Yao, Wu Wu, Yongjun Wu, Yiming Yan, Zhen Feng, Feifei Yu, Songcheng Wang, Wei |
author_sort | Wang, Sihua |
collection | PubMed |
description | Human protection of telomeres 1 (POT1) gene is a single stranded telomere binding proteins with a critical role in ensuring chromosome stability. There have been variants of POT1 gene, and the polymorphisms of POT1 gene were associated with some diseases. Polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) is a traditional method to detect the single nucleotide polymorphism (SNP), and it can be used to detect the polymorphism of rs10250202. But the restriction enzymes required for the detection of the polymorphism of rs10250202 are expensive. So we designed a novel PCR–RFLP assay for genotyping the POT1 rs10250202 SNP. In the study, a new restriction enzyme cutting site was created by created restriction site PCR (CRS-PCR), and the restriction enzyme BclI for CRS-PCR was cheaper than other enzymes. After detecting Han Chinese workers, Allele frequencies were found to be 51.54 % for allele A and 48.46 % for allele C respectively. The PCR results were confirmed by DNA sequencing. CRS-PCR provides a simple, low-cost, practical, and reproducible method. |
format | Online Article Text |
id | pubmed-4864762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-48647622016-05-31 Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay Wang, Sihua Duan, Xiaoran Wang, Tuanwei Feng, Xiaolei Wang, Pengpeng Yao, Wu Wu, Yongjun Wu, Yiming Yan, Zhen Feng, Feifei Yu, Songcheng Wang, Wei Springerplus Research Human protection of telomeres 1 (POT1) gene is a single stranded telomere binding proteins with a critical role in ensuring chromosome stability. There have been variants of POT1 gene, and the polymorphisms of POT1 gene were associated with some diseases. Polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) is a traditional method to detect the single nucleotide polymorphism (SNP), and it can be used to detect the polymorphism of rs10250202. But the restriction enzymes required for the detection of the polymorphism of rs10250202 are expensive. So we designed a novel PCR–RFLP assay for genotyping the POT1 rs10250202 SNP. In the study, a new restriction enzyme cutting site was created by created restriction site PCR (CRS-PCR), and the restriction enzyme BclI for CRS-PCR was cheaper than other enzymes. After detecting Han Chinese workers, Allele frequencies were found to be 51.54 % for allele A and 48.46 % for allele C respectively. The PCR results were confirmed by DNA sequencing. CRS-PCR provides a simple, low-cost, practical, and reproducible method. Springer International Publishing 2016-05-11 /pmc/articles/PMC4864762/ /pubmed/27247888 http://dx.doi.org/10.1186/s40064-016-2214-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Wang, Sihua Duan, Xiaoran Wang, Tuanwei Feng, Xiaolei Wang, Pengpeng Yao, Wu Wu, Yongjun Wu, Yiming Yan, Zhen Feng, Feifei Yu, Songcheng Wang, Wei Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay |
title | Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay |
title_full | Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay |
title_fullStr | Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay |
title_full_unstemmed | Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay |
title_short | Detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for PCR–RFLP assay |
title_sort | detection of the rs10250202 polymorphism in protection of telomeres 1 gene through introducing a new restriction enzyme site for pcr–rflp assay |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864762/ https://www.ncbi.nlm.nih.gov/pubmed/27247888 http://dx.doi.org/10.1186/s40064-016-2214-5 |
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