ATB0/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis

S. Larriba, L. Sumoy, M. D. Ramos, J. Giménez, Xavier P. Estivill, T. Casals, V. Nunes

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The Na+-dependent amino acid transporter named ATB0 was previously found to be located in 19q13.3 by fluorescence in situ hybridisation. Genetic heterogeneity in the 19q13.2-13.4 region, syntenic to the Cystic Fibrosis Modulator Locus 1 (CFM1) in mouse, seemed to be associated to the intestinal phenotypic variation of cystic fibrosis (CF). We performed fine chromosomal mapping of ATB0 on radiation hybrid (RH) panels G3 and TNG. Based on the most accurate location results from TNG-RH panel, mapping analysis evidenced that ATB0 is localised between STS SHGC-13875 (D19S995) and STS SHGC-6138 in 19q13.3, that corresponds with the immediately telomeric/distal segment of the strongest linkage region within the human CFM1 (hCFM1) syntenic region. Regarding to the genomic structure and exon organisation, our results show that the ATB0 gene is organised into eight exons. The knowledge of the genomic structure allowed us to perform an exhaustive mutational analysis of the gene. Evaluation of the possible implication of ATB0 in the intestinal phenotype of CF was performed on the basis of the functional characteristics of the encoded protein, its apparent relevance to meconium ileus (MI) and position in relation to the hCFM1 syntenic region. We have analysed this gene in samples from CF patients with and without MI. Several sequence variations in the ATB0 gene were identified, although none of them seemed to be related to the intestinal phenotype of CF. Even though no particular allele or haplotype in ATB0 appears to be associated to CF-MI disease, new SNPs identified should be useful in segregation and linkage disequilibrium analyses in families affected by other disorders caused by the impairment of neutral amino acid transport.

Original languageEnglish
Pages (from-to)860-866
Number of pages7
JournalEuropean Journal of Human Genetics
Volume9
Issue number11
Publication statusPublished - 2001
Externally publishedYes

Fingerprint

Cystic Fibrosis
Phenotype
Meconium
Ileus
Genes
Radiation Hybrid Mapping
Exons
Neutral Amino Acids
Amino Acid Transport Systems
Genetic Heterogeneity
Linkage Disequilibrium
Fluorescence In Situ Hybridization
Haplotypes
Single Nucleotide Polymorphism
Alleles
Organizations
Proteins

Keywords

  • Association analysis
  • ATB/SLC1A5 gene
  • Cystic fibrosis
  • Gastrointestinal system

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

ATB0/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis. / Larriba, S.; Sumoy, L.; Ramos, M. D.; Giménez, J.; Estivill, Xavier P.; Casals, T.; Nunes, V.

In: European Journal of Human Genetics, Vol. 9, No. 11, 2001, p. 860-866.

Research output: Contribution to journalArticle

Larriba, S. ; Sumoy, L. ; Ramos, M. D. ; Giménez, J. ; Estivill, Xavier P. ; Casals, T. ; Nunes, V. / ATB0/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis. In: European Journal of Human Genetics. 2001 ; Vol. 9, No. 11. pp. 860-866.
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AU - Nunes, V.

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