Cloning and characterization of the mouse short-chain acyl-CoA dehydrogenase gene

Mammalian Genome

Volumn 7, Issue 4, 1996, Pages 262-264

  Kelly, C L ^a   Wood, P A ^a  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PRIACANTHUS HAMRUR;

ACYL COENZYME A DEHYDROGENASE; DNA; PRIMER DNA;

ANIMAL; ARTICLE; CHROMOSOME MAP; EXON; GENETICS; INTRON; MOLECULAR CLONING; MOLECULAR GENETICS; MOUSE; NUCLEOTIDE SEQUENCE;

ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASES; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; CLONING, MOLECULAR; DNA; DNA PRIMERS; EXONS; INTRONS; MICE; MOLECULAR SEQUENCE DATA;

EID: 0030120816     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900078     Document Type: Article

References (12)

1. Carter, M.E., Gulick, T., Moore, D.D., Kelly, D.P. (1994). A pleiotropic element in the medium-chain acyl-coenzyme A dehydrogenase gene promoter mediates transcriptional regulation by multiple nuclear receptor transcription factors and defines novel receptor-DNA binding motifs. Mol. Cell. Biol. 14, 4360-4372.
2. Davis, L.G., Dibner, M.D., Battey, J.F. (1986). Basic Methods in Molecular Biology. (New York: Elsevier Science Publishing Co., Inc.).
3. Feinberg, A.P., Vogelstein, B. (1983). A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 132, 6-13.
4. Hinsdale, M.E., Kelly, C.L., Wood, P.A. (1993). Null allele at Bcd-1 locus in BALB/cByJ mice is due to a deletion in the short-chain acyl-CoA dehydrogenase gene and results in missplicing of mRNA. Genomics 16, 605-611.
5. Kelly, C.L., Hinsdale, M.E., Wood, P.A. (1943). Cloning and characterization of mouse short-chain acyl-CoA dehydrogenase cDNA. Genomics 18, 137-140.
6. Sambrook, J., Fritsch, E.F., Maniatis, T. (1489). Molecular Cloning: A Laboratory Manual. (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press).
7. Prochazka, M., Leiter, E.H. (1986). A null activity variant found at the butyryl CoA dehydrogenase (Bcd-1) locus in BALB/cByJ subline. Mouse News Lett. 75, 31.
8. Roe, C.R., Coates, P.M. (1995). Mitochondrial fatty acid oxidation disorders. In The Metabolic and Molecular Bases of Inherited Disease, C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle, eds. (New York: McGraw-Hill, Inc.), pp. 1501-1533.
9. Sanger, F., Nicklen, S., Coulson, A.R. (1977). DNA sequencing with chain termination inhibitors. Proc. Natl. Acad. Sci. USA 75, 5463-5467.
10. Schiffer, S.P., Prochaska, M., Jezyk, P.F., Roderick, T.H., Yudhoff, M., Patterson, D.F. (1989). Organic aciduria and butryl CoA dehydrogenase deficiency in BALB/cByJ mice. Biochem. Genet. 27, 47-58.
11. Tolwani, R.J., Farmer, S.C., Kurtz, D.M., Johnson, K.R., Davisson, M.T., Hinsdale, M.E., Cresci, S., Kelly, D.P., Wood, P.A. (1996). Gene-promoter structure and chromosomal location of the mouse medium-chain acyl-CoA dehydrogenase gene. Gene, in press.
12. Wood, P.A., Amendt, B.A., Rhead, W.J., Millington, D.S., Inoue, F., Armstrong, D. (1989). Short-chain acyl-coenzyme A dehydrogenase deficiency in mice. Pediatr. Res. 25, 38-43.