Literature DB >> 10895257

Erythroid band 3 variants and disease.

L J Bruce1, M J Tanner.   

Abstract

This review describes some of the naturally occurring band 3 (AEI) variants and their association with disease. Southeast Asian Ovalocytic (SAO) band 3, an inactive and misfolded protein, is probably only maintained in certain populations because it provides protection against the cerebral form of malaria. Many mutations that cause instability of band 3, either at the mRNA or protein level, result in hereditary spherocytosis (HS). Some polymorphisms alter amino acid residues in the extracellular loops of band 3 and are associated with blood group antigens. A truncated form of AEI is expressed in kidney cells and certain AEI mutations are associated with distal renal tubular acidosis (dRTA). The molecular basis of these variants and their effect on the structure and function of band 3 are discussed. The association between band 3 and glycophorin A (GPA) and the structure/function changes of band 3 in the absence of GPA are also described.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10895257     DOI: 10.1053/beha.1999.0046

Source DB:  PubMed          Journal:  Baillieres Best Pract Res Clin Haematol


  9 in total

1.  High prevalence of Southeast Asian ovalocytosis in Malays with distal renal tubular acidosis.

Authors:  Narazah Mohd Yusoff; Hans Van Rostenberghe; Taku Shirakawa; Kaoru Nishiyama; Noryati Amin; Zainal Darus; Nik Zainal; Nizam Isa; Hiroyuki Nozu; Masafumi Matsuo
Journal:  J Hum Genet       Date:  2003-11-15       Impact factor: 3.172

2.  A substrate access tunnel in the cytosolic domain is not an essential feature of the solute carrier 4 (SLC4) family of bicarbonate transporters.

Authors:  Volodymyr Shnitsar; Jing Li; Xuyao Li; Charles Calmettes; Arghya Basu; Joseph R Casey; Trevor F Moraes; Reinhart A F Reithmeier
Journal:  J Biol Chem       Date:  2013-10-11       Impact factor: 5.157

3.  Membrane compartmentalization in Southeast Asian ovalocytosis red blood cells.

Authors:  Rossen Mirchev; Alexander Lam; David E Golan
Journal:  Br J Haematol       Date:  2011-07-27       Impact factor: 6.998

4.  Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations.

Authors:  Pa-Thai Yenchitsomanus; Saranya Kittanakom; Nanyawan Rungroj; Emmanuelle Cordat; Reinhart A F Reithmeier
Journal:  J Mol Genet Med       Date:  2005-11-16

Review 5.  Delivery of drugs bound to erythrocytes: new avenues for an old intravascular carrier.

Authors:  Carlos H Villa; Daniel C Pan; Sergei Zaitsev; Douglas B Cines; Donald L Siegel; Vladimir R Muzykantov
Journal:  Ther Deliv       Date:  2015-07

6.  CrVI exposure and biomarkers: Cr in erythrocytes in relation to exposure and polymorphisms of genes encoding anion transport proteins.

Authors:  Qingshan Qu; Xiaomei Li; Feiyun An; Guang Jia; Lanzeng Liu; Hiroko Watanabe-Meserve; Karen Koenig; Beverly Cohen; Max Costa; Nirmal Roy; Mianhua Zhong; Lung Chi Chen; Suhua Liu; Lei Yan
Journal:  Biomarkers       Date:  2008-08       Impact factor: 2.658

7.  Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak.

Authors:  Damien Barneaud-Rocca; Bernard Pellissier; Franck Borgese; Hélène Guizouarn
Journal:  Int J Cell Biol       Date:  2011-08-23

Review 8.  Cell physiology and molecular mechanism of anion transport by erythrocyte band 3/AE1.

Authors:  Michael L Jennings
Journal:  Am J Physiol Cell Physiol       Date:  2021-10-20       Impact factor: 4.249

Review 9.  Review. Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1.

Authors:  J C Ellory; H Guizouarn; F Borgese; L J Bruce; R J Wilkins; G W Stewart
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-01-27       Impact factor: 6.237

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.