SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families

• Published in: Human mutation 2000-04, Vol.15 (4), p.367-372
• Main Authors: Noguchi, Atsuko, Shoji, Yutaka, Koizumi, Akio, Takahashi, Tsutomu, Shoji, Yasuko, Matsumori, Mika, Kayo, Tsuyoshi, Ohata, Tomoaki, Wada, Yasuhiko, Yoshimura, Ihoko, Maisawa, Shunichi, Konishi, Mineo, Takasago, Yuhei, Takada, Goro
• Format: Article
• Language: English
• Subjects: 5' Untranslated Regions - genetics; Alleles; alternative splicing; Alternative Splicing - genetics; Amino Acid Metabolism, Inborn Errors - genetics; Amino Acid Transport Systems, Basic; Carrier Proteins - chemistry; Carrier Proteins - genetics; DNA Mutational Analysis - methods; Exons - genetics; Female; genomic structure; Humans; Introns - genetics; LPI; Lysine - genetics; Lysine - urine; lysinuric protein intolerance; Male; Membrane Proteins - chemistry; Membrane Proteins - genetics; mutational analysis; SLC7A7
• ISSN: 1059-7794; 1098-1004
• DOI: 10.1002/(SICI)1098-1004(200004)15:4<367::AID-HUMU9>3.0.CO;2-C

Lysinuric protein intolerance (LPI) is a rare inherited disease caused by defective transport of the dibasic amino acids at the basolateral membranes of epithelial cells in the renal tubules and small intestine. The metabolic defect leads to brain dysfunction caused by hyperammonemia with a functional impairment of the urea cycle. Recently, mutations in the human SLC7A7 cDNA coding for y+LAT‐1, which express dibasic amino acid transport activity, were reported to be responsible for LPI. In the present study, we examined the genomic structure of SLC7A7 by DNA sequencing of PCR products, and determined that the gene had 11 exons and 10 introns spanning about 18 kb of genomic DNA. We also identified an alternative RNA splicing at the 5′ untranslated region of the SLC7A7 mRNA in human peripheral blood leukocytes, cultured lymphoblasts, and fibroblasts. As a result of mutational analysis of SLC7A7 in three Japanese LPI families, we found a nonsense mutation (R410X), a splicing mutation(911+1G>A) in intron 4, and four silent polymorphisms (201C/T, 445A/G, 784C/T, 946T/C). Identification of the genomic structure of SLC7A7 may provide a molecular basis for a genetic survey for LPI. Hum Mutat 15:367–372, 2000. © 2000 Wiley‐Liss, Inc.