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针对HBB基因突变热点的高分辨率熔解曲线分析为孟加拉国所有常见以及大多数罕见的β-珠蛋白基因突变提供了一种可靠的筛查方法。

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.

作者信息

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

机构信息

Laboratory of Genetics and Genomics, Institute for Developing Science and Health Initiatives, Mohakhali, Dhaka, Bangladesh.

Infectious Diseases Laboratory, Institute for Developing Science and Health Initiatives, Mohakhali, Dhaka, Bangladesh.

出版信息

BMC Genet. 2018 Jan 2;19(1):1. doi: 10.1186/s12863-017-0594-3.

Abstract

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.

摘要

背景

孟加拉国位于全球地中海贫血带,该地带在β-珠蛋白基因中有一个明确的突变热点。孟加拉国β-地中海贫血特征和血红蛋白E特征的高携带频率,使得有必要采用一种可靠的基于DNA的携带者筛查方法,以补充血液学和电泳指标的使用,从而克服携带者筛查的障碍。考虑到这一点,本研究旨在建立一种基于高分辨率熔解(HRM)曲线的快速可靠的突变筛查方法,该方法针对南亚和东南亚国家的突变热点,涵盖HBB基因的外显子1(c.1 - c.92)、内含子1(c.92 + 1 - c.92 + 130)和外显子2的一部分(c.93 - c.217),该基因携带了孟加拉国超过95%的导致β-地中海贫血的突变等位基因。

结果

我们的HRM方法能够成功区分10种β-珠蛋白基因突变,即杂合状态下的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和c.135delC与野生型等位基因,这意味着该方法对于携带者筛查具有重要意义,因为这些突变中的前三种占孟加拉国总突变等位基因的约85%。此外,发现复合杂合突变的不同组合会产生与野生型等位基因以及彼此不同的熔解曲线。基于这些发现,将16个参考样本与41个未知样本并行运行,以使用HRM对β-地中海贫血样本进行直接基因分型。基于HRM的未知样本基因分型与测序结果显示100%一致。

结论

针对突变热点,HRM方法可成功应用于孟加拉国以及南亚和东南亚其他国家的β-地中海贫血携带者筛查。该方法可以作为血液学和电泳指标的有益补充,以避免假阳性和假阴性结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fd7/5751541/7410be20959e/12863_2017_594_Fig1_HTML.jpg

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