Literature DB >> 16409302

Impaired interaction of alpha-haemoglobin-stabilising protein with alpha-globin termination mutant in a yeast two-hybrid system.

Chairat Turbpaiboon1, Thawornchai Limjindaporn, Wiyada Wongwiwat, Yaowalak U-Pratya, Noppadol Siritanaratkul, Pa-thai Yenchitsomanus, Sarawut Jitrapakdee, Prapon Wilairat.   

Abstract

Alpha-thalassaemia caused by alpha-globin gene termination codon mutations (alphaT-globin) has been explained by their inherent mRNA instability and by oxidative damage arising from the presence of membrane-bound alphaT-globin chains. To better understand the latter phenomenon, a yeast two-hybrid system was used to assay the interaction between alphaT-globin and its molecular chaperone, alpha-haemoglobin-stabilising protein (AHSP) and impaired binding of alphaT-globin with AHSP compared with alpha(wild-type)-globin was observed.

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Year:  2006        PMID: 16409302     DOI: 10.1111/j.1365-2141.2005.05865.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  11 in total

1.  Insights into hemoglobin assembly through in vivo mutagenesis of α-hemoglobin stabilizing protein.

Authors:  Eugene Khandros; Todd L Mollan; Xiang Yu; Xiaomei Wang; Yu Yao; Janine D'Souza; David A Gell; John S Olson; Mitchell J Weiss
Journal:  J Biol Chem       Date:  2012-01-27       Impact factor: 5.157

2.  Iron deficiency anemia interfering the diagnosis of compound heterozygosity for Hb constant spring and Hb Paksé: The first case report.

Authors:  Thita Chiasakul; Noppacharn Uaprasert
Journal:  J Clin Lab Anal       Date:  2017-02-28       Impact factor: 2.352

3.  Mutation near the binding interfaces at α-hemoglobin stabilizing protein is highly pathogenic.

Authors:  Jesu Francis Borgio; Mohammed S Al-Madan; Sayed AbdulAzeez
Journal:  Am J Transl Res       Date:  2016-10-15       Impact factor: 4.060

Review 4.  Hemoglobin variants: biochemical properties and clinical correlates.

Authors:  Christopher S Thom; Claire F Dickson; David A Gell; Mitchell J Weiss
Journal:  Cold Spring Harb Perspect Med       Date:  2013-03-01       Impact factor: 6.915

5.  Analysis of human alpha globin gene mutations that impair binding to the alpha hemoglobin stabilizing protein.

Authors:  Xiang Yu; Todd L Mollan; Andrew Butler; Andrew J Gow; John S Olson; Mitchell J Weiss
Journal:  Blood       Date:  2009-04-06       Impact factor: 22.113

6.  Hb H disease resulting from the association of an α-thalassemia allele [-(α)] with an unstable α-globin variant [Hb Icaria]: First report on the occurrence in Brazil.

Authors:  Elza M Kimura; Denise M Oliveira; Kleber Fertrin; Valéria R Pinheiro; Susan E D C Jorge; Fernando F Costa; Maria de Fátima Sonati
Journal:  Genet Mol Biol       Date:  2009-12-01       Impact factor: 1.771

7.  Alpha-hemoglobin-stabilizing protein: an erythroid molecular chaperone.

Authors:  Maria Emília Favero; Fernando Ferreira Costa
Journal:  Biochem Res Int       Date:  2011-03-24

Review 8.  Faithful chaperones.

Authors:  Ewa Szolajska; Jadwiga Chroboczek
Journal:  Cell Mol Life Sci       Date:  2011-06-08       Impact factor: 9.261

9.  α-Thalassemia associated with hb instability: a tale of two features. the case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro.

Authors:  Maria Grazia Bisconte; Mercedes Caldora; Gennaro Musollino; Giovanna Cardiero; Angela Flagiello; Gaetana La Porta; Laura Lagona; Romeo Prezioso; Gabriele Qualtieri; Carlo Gaudiano; Emilia Medulla; Antonello Merlino; Piero Pucci; Giuseppina Lacerra
Journal:  PLoS One       Date:  2015-03-02       Impact factor: 3.240

10.  Role of α-globin H helix in the building of tetrameric human hemoglobin: interaction with α-hemoglobin stabilizing protein (AHSP) and heme molecule.

Authors:  Elisa Domingues-Hamdi; Corinne Vasseur; Jean-Baptiste Fournier; Michael C Marden; Henri Wajcman; Véronique Baudin-Creuza
Journal:  PLoS One       Date:  2014-11-04       Impact factor: 3.240

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