Analysis of a1 and a2 globin genes among patients with hemoglobin Adana in Malaysia

Hemoglobin (Hb) Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a non-deletional α-thalassemia variant found in Malaysia. An improvement in the molecular techniques in recent years has made identification of Hb Adana much easier. For this study, a total of 26 Hb Adana α-thalassemia intermedia and...

Full description

Saved in:
Bibliographic Details
Main Authors: Lee, T. Y., Lai, M. I., Ismail, P., Ramachandran, V., Tan, J. A. M. A., Teh, L. K., Othman, R., Hussein, N. H., George, E.
Format: Article
Language:English
Published: Fundacao de Pesquisas Cientificas de Ribeirao Preto 2016
Online Access:http://psasir.upm.edu.my/id/eprint/43750/1/Analysis%20of%20%CE%B11%20and%20%CE%B12%20globin%20genes%20among%20patients%20with%20hemoglobin%20Adana%20in%20Malaysia.pdf
http://psasir.upm.edu.my/id/eprint/43750/
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Hemoglobin (Hb) Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a non-deletional α-thalassemia variant found in Malaysia. An improvement in the molecular techniques in recent years has made identification of Hb Adana much easier. For this study, a total of 26 Hb Adana α-thalassemia intermedia and 10 Hb Adana trait blood samples were collected from patients. Common deletional and non-deletional α-thalassemia genotypes were determined using multiplex gap polymerase chain reaction (PCR) and multiplex ARMS PCR techniques. Identification of the Hb Adana location on the α-globin gene was carried out using genomic sequencing and the location of the mutation was confirmed via restriction fragment length polymorphism-PCR. Among the 36 samples, 24 (66.7%) had the -α3.7/αCd59α mutation, while the -α3.7/αCd59α mutation accounted for 2 samples (5.6%) and the remaining 10 (27.8%) samples were α/αCd59α. All 36 samples were found to have the Hb Adana mutation on the a2-globin gene. The position of the α-globin gene mutation found in our cases was similar to that reported in Indonesia (16%) but not to that in Turkey (0.6%). Our results showed that the Hb Adana mutation was preferentially present in the a2-globin genes in Malays compared to the other ethnicities in Malaysia. Thus, the Malays might have similar ancestry based on the similarities in the Hb Adana position.