Literature DB >> 8102917

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes.

S Wang1, J H Nadeau, A Duncan, M F Robert, G Fontaine, K Schappert, K R Johnson, E Zietkiewicz, P Hruz, H Miziorko.   

Abstract

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL) is a homodimeric mitochondrial matrix enzyme that catalyzes the last step of ketogenesis. Using a human HL cDNA as a probe, we isolated a 1.4-kb mouse HL cDNA (HLM) from a mouse liver library and extended the sequence in the 5' direction, using RACE PCR to include the complete coding sequence. The nucleotide sequence of the mouse HL coding region is 85.7% identical to human HL, and 52.6% to Ps. mevalonii HL. Peptide identities of 87.4% and 54.3% respectively were observed. Southern analysis of 29 strains of laboratory mice and of Mus spretus revealed a total of about 25 kb of hybridizing fragments and three polymorphic fragments in both EcoRI and Hin-dIII digestions. The mouse HL locus (Hmgcl) was localized on Chromosome (Chr) 4: Pmv-19-12.6 +/- 3.6 cM-Hmgcl-7.3 +/- 2.3 cM-Xmv-8-1.5 +/- 1.0 cM-Gpd-1. The human HL locus (HMGCL) was mapped to distal Chr 1p by analysis of a human-hamster hybrid cell panel and by in situ hybridization.

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Year:  1993        PMID: 8102917     DOI: 10.1007/bf00360589

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  16 in total

Review 1.  Mouse chromosome 4.

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10.  3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency.

Authors:  G A Mitchell; M F Robert; P W Hruz; S Wang; G Fontaine; C E Behnke; L M Mende-Mueller; K Schappert; C Lee; K M Gibson; H M Miziorko
Journal:  J Biol Chem       Date:  1993-02-25       Impact factor: 5.157

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  8 in total

1.  Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway.

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Journal:  Mol Biol Rep       Date:  2011-09-28       Impact factor: 2.316

2.  Characterization of the hydroxymethylglutaryl-CoA lyase precursor, a protein targeted to peroxisomes and mitochondria.

Authors:  L I Ashmarina; M F Robert; M A Elsliger; G A Mitchell
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3.  A nonsense mutation in the 3-hydroxy-3-methylglutaryl-CoA lyase gene produces exon skipping in two patients of different origin with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

Authors:  J Pié; N Casals; C H Casale; C Buesa; C Mascaró; A Barceló; M O Rolland; T Zabot; D Haro; F Eyskens; P Divry; F G Hegardt
Journal:  Biochem J       Date:  1997-04-15       Impact factor: 3.857

4.  HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q.

Authors:  G A Mitchell; P T Ozand; M F Robert; L Ashmarina; J Roberts; K M Gibson; R J Wanders; S Wang; I Chevalier; E Plöchl; H Miziorko
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

5.  Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.

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Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

6.  Molecular cloning of rat mitochondrial 3-hydroxy-3-methylglutaryl-CoA lyase and detection of the corresponding mRNA and of those encoding the remaining enzymes comprising the ketogenic 3-hydroxy-3-methylglutaryl-CoA cycle in central nervous system of suckling rat.

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Journal:  Biochem J       Date:  1998-01-15       Impact factor: 3.857

7.  Molecular basis of 3-hydroxy-3-methylglutaric aciduria.

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8.  Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.

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  8 in total

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