This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow P3Rs: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when P3Rs are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via ISI Web of Science (10)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cheidde, L.
Right arrow Articles by Heilberg, I. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cheidde, L.
Right arrow Articles by Heilberg, I. P.
Related Collections
Right arrow Genitourinary Tract
PEDIATRICS Vol. 112 No. 6 December 2003, pp. 1361-1367

A Novel Mutation in the Anion Exchanger 1 Gene Is Associated With Familial Distal Renal Tubular Acidosis and Nephrocalcinosis

Lara Cheidde, MD, MSc*, Teresa Cristina Vieira, MD, PhD{ddagger}, Paulo Roberto Moura Lima, PhD§, Sara Teresinha Ollala Saad, MD, PhD§ and Ita Pfeferman Heilberg, MD, PhD*

* Nephrology Division, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil
{ddagger} Endocrinology Division, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil
§ Hemocentro, Faculdade de Ciências Médicas de Campinas, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil

Objective. The anion exchanger gene (AE1) or band 3 encodes a chloride-bicarbonate (Cl/HCO3) exchanger expressed in the erythrocyte and in the renal {alpha}-intercalated cells involved in urine acidification. The purpose of the present study was to screen for mutations in the AE1 gene in 2 brothers (10 and 15 years of age) with familial distal renal tubular acidosis (dRTA), nephrocalcinosis, and failure to thrive.

Methods. AE1 mutations were screened by single-strand conformation polymorphism, cloning, and sequencing.

Results. A complete form of dRTA was confirmed in the 2 affected brothers and an incomplete form in their father. All 3 were heterozygous for a novel 20-bp deletion in exon 20 of the AE1 gene. This deletion resulted in 1 mutation in codon 888 (Ala-888->Leu) followed by a premature termination codon at position 889, truncating the protein by 23 amino acids. As band 3 deficiency might lead to spherocytic hemolytic anemia or ovalocytosis, erythrocyte abnormalities were also investigated, but no morphologic changes in erythrocyte membrane were found and the osmotic fragility test was normal.

Conclusions. A novel mutation in the AE1 gene was identified in association with autosomal dominant dRTA. We suggest that RTA be considered a diagnostic possibility in all children with failure to thrive and nephrocalcinosis.


Key Words: distal renal tubular acidosis • nephrocalcinosis • anion exchanger 1 • band 3

Abbreviations: NC, nephrocalcinosis • dRTA, distal renal tubular acidosis • CA II, cytoplasmic carbonic anhydrase II • uRBP, urinary retinol binding protein • SSCP, single-strand conformation polymorphism • PCR, polymerase chain reaction


Received for publication Sep 18, 2002; Accepted Mar 16, 2003.




This article has been cited by other articles:


Home page
PhysiologyHome page
A. C. Fry and F. E. Karet
Inherited Renal Acidoses
Physiology, June 1, 2007; 22(3): 202 - 211.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
A. Pushkin and I. Kurtz
SLC4 base (HCO3-, CO32-) transporters: classification, function, structure, genetic diseases, and knockout models
Am J Physiol Renal Physiol, March 1, 2006; 290(3): F580 - F599.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Kittanakom, E. Cordat, V. Akkarapatumwong, P.-t. Yenchitsomanus, and R. A. F. Reithmeier
Trafficking Defects of a Novel Autosomal Recessive Distal Renal Tubular Acidosis Mutant (S773P) of the Human Kidney Anion Exchanger (kAE1)
J. Biol. Chem., September 24, 2004; 279(39): 40960 - 40971.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. Rungroj, M. A. J. Devonald, A. W. Cuthbert, F. Reimann, V. Akkarapatumwong, P.-t. Yenchitsomanus, W. M. Bennett, and F. E. Karet
A Novel Missense Mutation in AE1 Causing Autosomal Dominant Distal Renal Tubular Acidosis Retains Normal Transport Function but Is Mistargeted in Polarized Epithelial Cells
J. Biol. Chem., April 2, 2004; 279(14): 13833 - 13838.
[Abstract] [Full Text] [PDF]