Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression

Genomics

Volumn 72, Issue 2, 2001, Pages 145-152

  Obata, Keiko ^a   Fukuda, Takayuki ^a   Morishita, Riyo ^a   Abe, Shunnosuke ^b   Asakawa, Shuichi ^c   Yamaguchi, Seiji ^d   Yoshino, Makoto ^e   Ihara, Kenji ^f   Murayama, Keiko ^g   Shigemoto, Kazuhiro ^a   Shimizu, Nobuyoshi ^c   Kondo, Ikuko ^a  

^a EHIME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b EHIME UNIVERSITY   (Japan)

^c KEIO UNIVERSITY   (Japan)

^d SHIMANE UNIVERSITY   (Japan)

^e KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f KYUSHU UNIVERSITY   (Japan)

^g National Rehabilitation Center for the Disabled   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTIN; METHYLCROTONOYL COENZYME A CARBOXYLASE; RECEPTOR SUBUNIT;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CATABOLISM; CHROMOSOMAL LOCALIZATION; CHROMOSOME 3Q; CHROMOSOME MAP; DNA SEQUENCE; GENE EXPRESSION REGULATION; GENE MUTATION; GENETIC ORGANIZATION; HUMAN; HUMAN CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN;

ANIMALIA; ARABIDOPSIS THALIANA; BACTERIA (MICROORGANISMS); GLYCINE MAX; LYCOPERSICON ESCULENTUM; MAMMALIA;

EID: 0035280249     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6366     Document Type: Article

References (24)

1. Isolated biotin-resistant deficiency of 3-methyl-crotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome
2. Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency
3. Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with a deficiency of 3-methylcrotonyl-CoA carboxylase
4. 3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children
5. Survey of amino-terminal proteolytic cleavage sites in mitochondrial precursor proteins: Leader peptides cleaved by two matrix proteases share a three-amino acid motif
6. An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency detected by newborn screening for maple syrup urine disease
7. Two mitochondrial matrix proteases act sequentially in the processing of mammalian matrix enzymes
8. Interpreting cDNA sequences: Some insights from studies on translation
9. Bovine kidney 3-methylcrotonyl-CoA and propionyl-CoA enzyme carboxylase: Each enzyme contains nonidentical subunits
10. Isolation of 3-methylcrotonyl-coenzyme A carboxylase from bovine kidney
11. Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness
12. Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency: Long-term outcome in a case with neonatal onset
13. Molecular characterization of the non-biotin-containing subunit of 3-metylcrotonyl-CoA carboxylase
14. The biotin-dependent enzymes
15. Isolated 3-metylcrotonyl-CoA carboxylase deficiency in a 15-year-old girl
16. Deficiency of 3-metylglutaconyl-coenzyme A hydratase in two siblings with 3-metylglutaconic aciduria
17. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
18. Molecular cloning and characterization of the cDNA coding for the biotin-containing subunit of 3-methylcrotonoyl-CoA carboxylase: Identification of the biotin carboxylase and biotin-carrier domains
19. Branched chain organic acidurias
20. Two siblings with biotin-resistant 3-methylcrotonyl coenzyme A carboxylase deficiency
21. Molecular cloning of cDNA and genes coding for β-methylcrotonyl-CoA carboxylase of tomato
22. Molecular cloning of the biotinylated subunit of 3-methylcrotonyl-coenzyme A carboxylase of Arabidopsis thaliana