Human fatty aldehyde dehydrogenase gene (ALDH10): Organization and tissue-dependent expression

Genomics

Volumn 40, Issue 1, 1997, Pages 80-85

  Chang, Cheng ^a   Yoshida, Akira ^a  

^a CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DEHYDROGENASE; COMPLEMENTARY DNA; MESSENGER RNA; POLYADENYLATED RNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BINDING SITE; DNA FLANKING REGION; ENZYME ACTIVITY; GENE EXPRESSION; GENE MUTATION; GENOME; HUMAN; HUMAN TISSUE; LIPID METABOLISM; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SJOEGREN LARSSON SYNDROME; TISSUE SPECIFICITY; TRANSCRIPTION INITIATION;

EID: 0031568898     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.4547     Document Type: Article

References (23)

1. Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Smith, J. A., Seidman, J. G., and Struhl, K. (1987). "Current Protocols in Molecular Biology," Wiley, New York.
2. Breathnach, R., and Chambon, P. (1981). Organization and expression of eucaryotic split genes coding for proteins. Annu. Rev. Biochem. 50: 349-383.
3. o are produced by alternative polyadenylation in mouse. Eur. J. Biochem. 221: 421-425.
4. Bucher, P. (1990). Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences. J. Mol. Biol. 212: 563-578.
5. De Laurenzi, V., Rogers, G. R., Hamrock, D. J., Marekov, L. N., Steinert, P. M., Compton, J. G., Markova, N., and Rizzo, W. B. (1996). Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene. Nature Genet. 12: 52-57.
6. Hiraoka, L. R., Hsu, L., and Hsieh, C.-L. (1995). Assignment of ALDH3 to human chromosome 17p11.2 and ALDH5 to human chromosome 9p13. Genomics 25: 323-325.
7. Hsu, L. C., Chang, W.-C., Shibuya, A., and Yoshida, A. (1992). Human stomach aldehyde dehydrogenase cDNA and genomic cloning, primary structure, and expression in Escherichia coli. J. Biol. Chem. 267: 3030-3037.
8. Jagell, S., Gustavson, K.-H., and Holmgren, G. (1981). Sjögren-Larsson syndrome in Sweden: A clinical, genetic and epidemiological study. Clin. Genet. 19: 233-256.
9. Lindahl, R. (1992). Aldehyde dehydrogenases and their role in carcinogenesis. Crit. Rev. Biochem. Mol. Biol. 27: 283-335.
10. Lindahl, R., and Petersen, D. R. (1991). Lipid aldehyde oxidation as a physiological role for class 3 aldehyde dehydrogenases. Biochem. Pharmacol. 41: 1583-1587.
11. Means, A. L., and Farnham, P. J. (1990). Transcription initiation from the dihydrofolate reductase promoter is positioned by HIP1 binding at the initiation site. Mol. Cell. Biol. 10: 653-661.
12. Mitchell, D. Y., and Petersen, D. R. (1989). Oxidation of aldehyde products of lipid peroxidation by rat liver microsomal aldehyde dehydrogenase. Arch. Biochem. Biophys. 269: 11-17.
13. Miyauchi, K, Masaki, R., Taketani, S., Yamamoto, A., Akayama, M., and Tashiro, Y. (1991). Molecular cloning, sequencing, and expression of cDNA for rat liver microsomal aldehyde dehydrogenase. J. Biol. Chem. 266: 19536-19542.
14. Panchenko, L. F., Pirozhkov, S.V., and Antonenkov, V. D. (1985). Subcellular distribution and properties of a clofibrate-induced aldehyde dehydrogenase form rat liver. Biochem. Pharmacol. 34: 471-479.
15. Pigg, M., Jagell, S., Sillén, A., Weissenbach, J., Gustavson, K.-H., and Wadelius, C. (1994). The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic association. Nature Genet. 8: 361-364.
16. Regers, G. R., Rizzo, W. B., Zlotogorski, A., Hashem, N., Lee, M., Compton, J. G., and Bale, S. J. (1995). Genetic homogeneity in Sjögren-Larsson syndrome: Linkage to chromosome 17p in families of different non-Swedish ethnic origins. Am. J. Hum. Genet. 57: 1123-1129.
17. Rizzo, W. B. (1993). Sjögren-Larsson syndrome. Semin. Dermatol. 12: 210-218.
18. + oxidoreductase in cultured fibroblasts. J. Clin. Invest. 88: 1643-1648.
19. Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989). "Molecular Cloning: A Laboratory Manual," (2nd ed.), Cold Spring Habor Laboratory Press, Cold Spring Harbor, NY.
20. Sjögren, T., and Larsson, T. (1957). Oligophrenia in combination with congenital ichthyosis and spastic disorders. Acta Psychiatr. Neurol. Scand. 32: 1-113.
21. Vasiliou, V., Kozak, C. A., Lindahl, R., and Nebert, D. W. (1996). Mouse microsomal class 3 aldehyde dehydrogenase: AHD3 cDNA sequence, inducibility by dioxin and clofibrate, and genetic mapping. DNA Cell Biol. 15: 235-245.
22. Yasunami, M., Kikuchi, I., Sarapata, D., and Yoshida, A. (1990). The human class I alcohol dehydrogenase gene cluster: Three genes are tandemly organized in an 80-kb-long segment of the genome. Genomics 7: 152-158.
23. Yoshida, A. (1992). Molecular genetics of human aldehyde dehydrogenase. Phamacogenetics 2: 139-147.