Literature DB >> 1684944

Structure and expression of the human mitochondrial acetoacetyl-CoA thiolase-encoding gene.

M Kano1, T Fukao, S Yamaguchi, T Orii, T Osumi, T Hashimoto.   

Abstract

To examine 3-ketothiolase deficiency at the gene level, we analyzed the structure of the human mitochondrial acetoacetyl-CoA thiolase (MAT; EC 2.3.1.9)-encoding gene (MAT). From the genomic library of a normal subject in lambda EMBL3, we isolated seven overlapping clones covering the entire length of MAT and the structural organization was determined. The gene spans approx. 27 kb and contains twelve exons interrupted by eleven introns. The 5'-flanking region of the gene lacks a conventional TATA box, but is G + C-rich and contains two CAAT boxes. Included are a putative binding site for the transcription factor, Sp1, and sequences resembling the binding sites of several other transcription factors, all features characteristic of housekeeping genes. A CAT assay revealed that a 101-bp DNA fragment immediately upstream from the cap site has promoter activity, and suggested that a DNA fragment from bp -888 to -102 probably contains a negative regulatory element(s).

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Year:  1991        PMID: 1684944     DOI: 10.1016/0378-1119(91)90623-j

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  13 in total

1.  Molecular basis of 3-ketothiolase deficiency: detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolase.

Authors:  T Fukao; S Yamaguchi; A Wakazono; H Okamoto; T Orii; T Osumi; T Hashimoto
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Identification of TaqI polymorphism in the mitochondrial acetoacetyl-CoA thiolase gene and familial analysis of 3-ketothiolase deficiency.

Authors:  T Kuwahara; T Fukao; M Kano; S Yamaguchi; T Orii; T Hashimoto
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

3.  Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry.

Authors:  Toshiyuki Fukao; Shinsuke Maruyama; Toshihiro Ohura; Yuki Hasegawa; Mitsuo Toyoshima; Antti M Haapalainen; Naomi Kuwada; Mari Imamura; Isao Yuasa; Rik K Wierenga; Seiji Yamaguchi; Naomi Kondo
Journal:  JIMD Rep       Date:  2011-09-06

4.  CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1.

Authors:  X Chen; L Yang; N Udar; T Liang; N Uhrhammer; S Xu; J O Bay; Z Wang; S Dandakar; S Chiplunkar; I Klisak; M Telatar; H Yang; P Concannon; R A Gatti
Journal:  Mamm Genome       Date:  1997-02       Impact factor: 2.957

5.  Clinical and molecular analysis of 6 Chinese patients with isoleucine metabolism defects: identification of 3 novel mutations in the HSD17B10 and ACAT1 gene.

Authors:  Ling Su; Xiuzhen Li; Ruizhu Lin; Huiying Sheng; Zhichun Feng; Li Liu
Journal:  Metab Brain Dis       Date:  2017-09-05       Impact factor: 3.584

Review 6.  Disorders of mitochondrial fatty acyl-CoA beta-oxidation.

Authors:  R J Wanders; P Vreken; M E den Boer; F A Wijburg; A H van Gennip; L IJlst
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

7.  Identification of three mutant alleles of the gene for mitochondrial acetoacetyl-coenzyme A thiolase. A complete analysis of two generations of a family with 3-ketothiolase deficiency.

Authors:  T Fukao; S Yamaguchi; T Orii; R B Schutgens; T Osumi; T Hashimoto
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

8.  Identification of a novel exonic mutation at -13 from 5' splice site causing exon skipping in a girl with mitochondrial acetoacetyl-coenzyme A thiolase deficiency.

Authors:  T Fukao; S Yamaguchi; A Wakazono; T Orii; G Hoganson; T Hashimoto
Journal:  J Clin Invest       Date:  1994-03       Impact factor: 14.808

9.  Single-nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT1 gene.

Authors:  Hideo Sasai; Yuka Aoyama; Hiroki Otsuka; Elsayed Abdelkreem; Mina Nakama; Tomohiro Hori; Hidenori Ohnishi; Lesley Turner; Toshiyuki Fukao
Journal:  Mol Genet Genomic Med       Date:  2017-02-08       Impact factor: 2.183

10.  A Novel Mutation of Beta-ketothiolase Deficiency: The First Report from Iran and Review of Literature.

Authors:  Rahim Vakili; Somayyeh Hashemian
Journal:  Iran J Child Neurol       Date:  2018
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