Genomic structure and organization of the human rBAT gene (SLC3A1)
Cystinuria is an autosomal recessive disorder of amino acid transport, manifesting as three phenotypes (I, II, and III). An amino acid transport gene, rBAT, is responsible for cystinuria. Mutation and linkage analyses have demonstrated the disease to be heterogeneous, with rBAT being the defective g...
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Published in | Genomics (San Diego, Calif.) Vol. 37; no. 2; pp. 249 - 252 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier
15.10.1996
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Subjects | |
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Abstract | Cystinuria is an autosomal recessive disorder of amino acid transport, manifesting as three phenotypes (I, II, and III). An amino acid transport gene, rBAT, is responsible for cystinuria. Mutation and linkage analyses have demonstrated the disease to be heterogeneous, with rBAT being the defective gene in type I cystinuria. The genomic structure of the human rBAT gene (HGMW-approved symbol SLC 3A1) has been established via two strategies: (i) construction of two different genomic libraries by subcloning the Mega-YAC921B6 (CEPH), containing rBAT, in Lambda ZAP and screening using rBAT cDNA and different PCR products; and (ii) generation and sequencing of genomic fragments by long PCR using rBAT cDNA-derived primers. The rBAT gene spans approximately 45 kb and consists of 10 exons. The introns range from 500 to 13,000 bp. All splice sites conform to the GT/AG rule. The promoter region has been further analyzed, and a predicted TATA box 98 bp upstream of the first coding ATG was identified. In addition an Alu repeat has been detected 72 bp upstream of the predicted TATA box. |
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AbstractList | Cystinuria is an autosomal recessive disorder of amino acid transport, manifesting as three phenotypes (I, II, and III). An amino acid transport gene, rBAT, is responsible for cystinuria. Mutation and linkage analyses have demonstrated the disease to be heterogeneous, with rBAT being the defective gene in type I cystinuria. The genomic structure of the human rBAT gene (HGMW-approved symbol SLC 3A1) has been established via two strategies: (i) construction of two different genomic libraries by subcloning the Mega-YAC921B6 (CEPH), containing rBAT, in Lambda ZAP and screening using rBAT cDNA and different PCR products; and (ii) generation and sequencing of genomic fragments by long PCR using rBAT cDNA-derived primers. The rBAT gene spans approximately 45 kb and consists of 10 exons. The introns range from 500 to 13,000 bp. All splice sites conform to the GT/AG rule. The promoter region has been further analyzed, and a predicted TATA box 98 bp upstream of the first coding ATG was identified. In addition an Alu repeat has been detected 72 bp upstream of the predicted TATA box. |
Author | CALONGE, M. J PURROY, J ZELANTE, L GASPARINI, P ZORZANO, A BISCEGLIA, L ESTIVILL, X NUNES, V PALACIN, M TESTAR, X |
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Keywords | Human Urinary system disease Nucleotide sequence Transcription promoter Biological transport Tubulopathy Metabolic diseases Renal disease Gene organization Cystinuria Genetic disease Gene Aminoacid Chromosome DNA Genetics Aminoacid disorder Aminoaciduria |
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Snippet | Cystinuria is an autosomal recessive disorder of amino acid transport, manifesting as three phenotypes (I, II, and III). An amino acid transport gene, rBAT, is... |
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SubjectTerms | Amino Acid Transport Systems, Basic Biological and medical sciences Carrier Proteins - genetics Cystinuria - genetics Exons Fundamental and applied biological sciences. Psychology Genes. Genome Genome, Human Humans Introns Membrane Glycoproteins - genetics Molecular and cellular biology Molecular genetics Polymerase Chain Reaction |
Title | Genomic structure and organization of the human rBAT gene (SLC3A1) |
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