CHARACTERIZATION OF THE GENE ENCODING HUMAN PEROXISOMAL 3-OXOACYL-COA THIOLASE (ACAA) - NO LARGE DNA REARRANGEMENT IN A THIOLASE-DEFICIENT PATIENT

被引:31
作者
BOUT, A
FRANSE, MM
COLLINS, J
BLONDEN, L
TAGER, JM
BENNE, R
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,EC SLATER INST BIOCHEM RES,MEIBERGDREEF 15,1105 AZ AMSTERDAM,NETHERLANDS
[2] YESHIVA UNIV ALBERT EINSTEIN COLL MED,BRONX,NY 10461
[3] LEIDEN UNIV,2300 RA LEIDEN,NETHERLANDS
关键词
GENE CHARACTERIZATION; 3-OXOACYL-COA; THIOLASE DEFICIENCY; BETA-OXIDATION; PEROXISOME; (HUMAN);
D O I
10.1016/0167-4781(91)90035-K
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have characterized the gene encoding human peroxisomal 3-oxoacyl-CoA thiolase, an enzyme operative in the peroxisomal beta-oxidation system. We found one version of this gene (gene symbol ACAA) in the human genome, in contrast to the situation in rat where two versions have been described. The human gene shows a high structural similarity to the rat genes. It contains 12 exons and 11 introns and spans about 11 kb. We have determined the 5' end of the human thiolase mRNA by employing primer extension analysis and we have sequenced the region upstream of the gene. The putative promoter area displays some of the characteristics typical of promoters of other peroxisomal genes, in that it contains GC elements, but lacks TATA boxes. Finally, no large DNA rearrangement involving the thiolase gene could be observed in a patient suffering from pseudo-Zellweger syndrome (peroxisomal thiolase deficiency).
引用
收藏
页码:43 / 51
页数:9
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