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High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh
BACKGROUND: Bangladesh lies in the global thalassemia belt, which has a defined mutational hot-spot in the beta-globin gene. The high carrier frequencies of beta-thalassemia trait and hemoglobin E-trait in Bangladesh necessitate a reliable DNA-based carrier screening approach that could supplement t...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751541/ https://www.ncbi.nlm.nih.gov/pubmed/29295702 http://dx.doi.org/10.1186/s12863-017-0594-3 |
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author | Islam, Md Tarikul Sarkar, Suprovath Kumar Sultana, Nusrat Begum, Mst. Noorjahan Bhuyan, Golam Sarower Talukder, Shezote Muraduzzaman, A. K. M. Alauddin, Md Islam, Mohammad Sazzadul Biswas, Pritha Promita Biswas, Aparna Qadri, Syeda Kashfi Shirin, Tahmina Banu, Bilquis Sadya, Salma Hussain, Manzoor Sarwardi, Golam Khan, Waqar Ahmed Mannan, Mohammad Abdul Shekhar, Hossain Uddin Chowdhury, Emran Kabir Sajib, Abu Ashfaqur Akhteruzzaman, Sharif Qadri, Syed Saleheen Qadri, Firdausi Mannoor, Kaiissar |
author_facet | Islam, Md Tarikul Sarkar, Suprovath Kumar Sultana, Nusrat Begum, Mst. Noorjahan Bhuyan, Golam Sarower Talukder, Shezote Muraduzzaman, A. K. M. Alauddin, Md Islam, Mohammad Sazzadul Biswas, Pritha Promita Biswas, Aparna Qadri, Syeda Kashfi Shirin, Tahmina Banu, Bilquis Sadya, Salma Hussain, Manzoor Sarwardi, Golam Khan, Waqar Ahmed Mannan, Mohammad Abdul Shekhar, Hossain Uddin Chowdhury, Emran Kabir Sajib, Abu Ashfaqur Akhteruzzaman, Sharif Qadri, Syed Saleheen Qadri, Firdausi Mannoor, Kaiissar |
author_sort | Islam, Md Tarikul |
collection | PubMed |
description | BACKGROUND: Bangladesh lies in the global thalassemia belt, which has a defined mutational hot-spot in the beta-globin gene. The high carrier frequencies of beta-thalassemia trait and hemoglobin E-trait in Bangladesh necessitate a reliable DNA-based carrier screening approach that could supplement the use of hematological and electrophoretic indices to overcome the barriers of carrier screening. With this view in mind, the study aimed to establish a high resolution melting (HRM) curve-based rapid and reliable mutation screening method targeting the mutational hot-spot of South Asian and Southeast Asian countries that encompasses exon-1 (c.1 - c.92), intron-1 (c.92 + 1 - c.92 + 130) and a portion of exon-2 (c.93 - c.217) of the HBB gene which harbors more than 95% of mutant alleles responsible for beta-thalassemia in Bangladesh. RESULTS: Our HRM approach could successfully differentiate ten beta-globin gene mutations, namely c.79G > A, c.92 + 5G > C, c.126_129delCTTT, c.27_28insG, c.46delT, c.47G > A, c.92G > C, c.92 + 130G > C, c.126delC and c.135delC in heterozygous states from the wild type alleles, implying the significance of the approach for carrier screening as the first three of these mutations account for ~85% of total mutant alleles in Bangladesh. Moreover, different combinations of compound heterozygous mutations were found to generate melt curves that were distinct from the wild type alleles and from one another. Based on the findings, sixteen reference samples were run in parallel to 41 unknown specimens to perform direct genotyping of the beta-thalassemia specimens using HRM. The HRM-based genotyping of the unknown specimens showed 100% consistency with the sequencing result. CONCLUSIONS: Targeting the mutational hot-spot, the HRM approach could be successfully applied for screening of beta-thalassemia carriers in Bangladesh as well as in other countries of South Asia and Southeast Asia. The approach could be a useful supplement of hematological and electrophortic indices in order to avoid false positive and false negative results. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-017-0594-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5751541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57515412018-01-05 High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh Islam, Md Tarikul Sarkar, Suprovath Kumar Sultana, Nusrat Begum, Mst. Noorjahan Bhuyan, Golam Sarower Talukder, Shezote Muraduzzaman, A. K. M. Alauddin, Md Islam, Mohammad Sazzadul Biswas, Pritha Promita Biswas, Aparna Qadri, Syeda Kashfi Shirin, Tahmina Banu, Bilquis Sadya, Salma Hussain, Manzoor Sarwardi, Golam Khan, Waqar Ahmed Mannan, Mohammad Abdul Shekhar, Hossain Uddin Chowdhury, Emran Kabir Sajib, Abu Ashfaqur Akhteruzzaman, Sharif Qadri, Syed Saleheen Qadri, Firdausi Mannoor, Kaiissar BMC Genet Research Article BACKGROUND: Bangladesh lies in the global thalassemia belt, which has a defined mutational hot-spot in the beta-globin gene. The high carrier frequencies of beta-thalassemia trait and hemoglobin E-trait in Bangladesh necessitate a reliable DNA-based carrier screening approach that could supplement the use of hematological and electrophoretic indices to overcome the barriers of carrier screening. With this view in mind, the study aimed to establish a high resolution melting (HRM) curve-based rapid and reliable mutation screening method targeting the mutational hot-spot of South Asian and Southeast Asian countries that encompasses exon-1 (c.1 - c.92), intron-1 (c.92 + 1 - c.92 + 130) and a portion of exon-2 (c.93 - c.217) of the HBB gene which harbors more than 95% of mutant alleles responsible for beta-thalassemia in Bangladesh. RESULTS: Our HRM approach could successfully differentiate ten beta-globin gene mutations, namely c.79G > A, c.92 + 5G > C, c.126_129delCTTT, c.27_28insG, c.46delT, c.47G > A, c.92G > C, c.92 + 130G > C, c.126delC and c.135delC in heterozygous states from the wild type alleles, implying the significance of the approach for carrier screening as the first three of these mutations account for ~85% of total mutant alleles in Bangladesh. Moreover, different combinations of compound heterozygous mutations were found to generate melt curves that were distinct from the wild type alleles and from one another. Based on the findings, sixteen reference samples were run in parallel to 41 unknown specimens to perform direct genotyping of the beta-thalassemia specimens using HRM. The HRM-based genotyping of the unknown specimens showed 100% consistency with the sequencing result. CONCLUSIONS: Targeting the mutational hot-spot, the HRM approach could be successfully applied for screening of beta-thalassemia carriers in Bangladesh as well as in other countries of South Asia and Southeast Asia. The approach could be a useful supplement of hematological and electrophortic indices in order to avoid false positive and false negative results. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-017-0594-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-02 /pmc/articles/PMC5751541/ /pubmed/29295702 http://dx.doi.org/10.1186/s12863-017-0594-3 Text en © The Author(s). 2018 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Islam, Md Tarikul Sarkar, Suprovath Kumar Sultana, Nusrat Begum, Mst. Noorjahan Bhuyan, Golam Sarower Talukder, Shezote Muraduzzaman, A. K. M. Alauddin, Md Islam, Mohammad Sazzadul Biswas, Pritha Promita Biswas, Aparna Qadri, Syeda Kashfi Shirin, Tahmina Banu, Bilquis Sadya, Salma Hussain, Manzoor Sarwardi, Golam Khan, Waqar Ahmed Mannan, Mohammad Abdul Shekhar, Hossain Uddin Chowdhury, Emran Kabir Sajib, Abu Ashfaqur Akhteruzzaman, Sharif Qadri, Syed Saleheen Qadri, Firdausi Mannoor, Kaiissar High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh |
title | High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh |
title_full | High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh |
title_fullStr | High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh |
title_full_unstemmed | High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh |
title_short | High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh |
title_sort | high resolution melting curve analysis targeting the hbb gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in bangladesh |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751541/ https://www.ncbi.nlm.nih.gov/pubmed/29295702 http://dx.doi.org/10.1186/s12863-017-0594-3 |
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