Literature DB >> 21269848

Enzymatic and metabolic characterization of the phosphoglycerate kinase deficiency associated with chronic hemolytic anemia caused by the PGK-Barcelona mutation.

María José Ramírez-Bajo1, Ada Repiso, Pablo Pérez de la Ossa, Elisenda Bañón-Maneus, Pedro de Atauri, Fernando Climent, Joan-Lluís Vives Corrons, Marta Cascante, José Carreras.   

Abstract

Recently, we reported a new mutation of phosphoglycerate kinase (PGK), called PGK-Barcelona, which causes chronic hemolytic anemia associated with progressive neurological impairment. We found a 140T→A substitution that produces an Ile46Asn change located at the N-domain of the enzyme and we suggested that the decrease of the PGK activity is probably related to a loss of enzyme stability. In this paper, by analyzing whole hemolysates and cloned enzymes, we show that both enzymes possess similar kinetic properties (although some differences are observed in the Km values) and the same electrophoretic mobility. However, PGK-Barcelona has higher thermal instability. Therefore, we confirm that the decrease of the red blood cell (RBC) PGK activity caused by the PGK-Barcelona mutation is more closely related to a loss of enzyme stability than to a decrease of enzyme catalytic function. Furthermore, we have measured the levels of glycolytic metabolites and adenine nucleotides in the RBC from controls and from the patient. The increase of 2,3-bisphosphoglycerate and the decrease of ATP RBC levels are the only detected metabolic changes that could cause hemolytic anemia.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21269848     DOI: 10.1016/j.bcmd.2010.12.009

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  5 in total

1.  A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria.

Authors:  Shigeto Matsumaru; Hirokazu Oguni; Hiromi Ogura; Keiko Shimojima; Satoru Nagata; Hitoshi Kanno; Toshiyuki Yamamoto
Journal:  Intractable Rare Dis Res       Date:  2017-05

2.  Phosphoglycerate kinase deficiency due to a novel mutation (c. 1180A>G) manifesting as chronic hemolytic anemia in a Japanese boy.

Authors:  Masato Tamai; Takeshi Kawano; Ryota Saito; Ken Sakurai; Yoshihiro Saito; Hisashi Yamada; Hiroyuki Ida; Masaharu Akiyama
Journal:  Int J Hematol       Date:  2014-06-17       Impact factor: 2.490

3.  Molecular insights on pathogenic effects of mutations causing phosphoglycerate kinase deficiency.

Authors:  Laurent R Chiarelli; Simone M Morera; Paola Bianchi; Elisa Fermo; Alberto Zanella; Alessandro Galizzi; Giovanna Valentini
Journal:  PLoS One       Date:  2012-02-14       Impact factor: 3.240

4.  Insulin and mTOR Pathway Regulate HDAC3-Mediated Deacetylation and Activation of PGK1.

Authors:  Shiwen Wang; Bowen Jiang; Tengfei Zhang; Lixia Liu; Yi Wang; Yiping Wang; Xiufei Chen; Huaipeng Lin; Lisha Zhou; Yukun Xia; Leilei Chen; Chen Yang; Yue Xiong; Dan Ye; Kun-Liang Guan
Journal:  PLoS Biol       Date:  2015-09-10       Impact factor: 8.029

5.  A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population.

Authors:  Virginia Garcia-Solaesa; Pablo Serrano-Lorenzo; Maria Antonia Ramos-Arroyo; Alberto Blázquez; Inmaculada Pagola-Lorz; Mercè Artigas-López; Joaquín Arenas; Miguel A Martín; Ivonne Jericó-Pascual
Journal:  Genes (Basel)       Date:  2019-10-10       Impact factor: 4.096

  5 in total

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