Please use this identifier to cite or link to this item: http://ir.swu.ac.th/jspui/handle/123456789/15296
Title: Relative quantitation of mRNA in β-thalassemia/Hb E using real-time polymerase chain reaction
Authors: Watanapokasin Y.
Winichagoon P.
Fuchareon S.
Wilairat P.
Keywords: alpha globin
beta globin
hemoglobin E
messenger RNA
article
beta thalassemia
clinical article
controlled study
disease severity
gene sequence
hemoglobin determination
hemoglobinopathy
human
human cell
pathogenesis
polymerase chain reaction
reticulocyte
RNA analysis
RNA splicing
Issue Date: 2000
Abstract: β-Thalassemia and Hb E patients, with seemingly identical genotypes, have a remarkable variability in severity. Reduction in red cell survival in β-thalassemia is correlated with the amount of intracellular unmatched α- globin chains. However, it was only recently realized that mRNA, whose translation is prematurely terminated, is also unstable. No systematic attempts have been made to investigate mRNA stability in β-thalassemia arising from nonsense mutations located upstream from the normal termination codon. In this study, one-step real-time polymerase chain reaction has been employed to compare the levels of α- and β-globin mRNA in reticulocytes from β-thalassemia/Hb E subjects. The results showed the highest α/β- globin mRNA ratio (median = 5.70, n = 13) in frameshift codons 41/42 (- TTCT)/Hb E individuals compared to normal subjects (median = 1.02, n = 6), or those with Hb E trait (median = 2.15, n = 8). In addition, there was a concomitant increase in the α/β-globin mRNA ratio with decrease in hemoglobin level, i.e., increase in severity. The difference in the ratio among β-thalassemia/Hb E patients with the same genotype may be attributed to individual variations of efficiency in β(E)-globin mRNA splicing and in the destruction of prematurely terminated mRNA.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034092252&doi=10.3109%2f03630260009003429&partnerID=40&md5=28b5c16a0a40c207ff4cc33ad2cfdffc
http://ir.swu.ac.th/jspui/handle/123456789/15296
ISSN: 3630269
Appears in Collections:Scopus 1983-2021

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