Literature DB >> 2265838

The gene coding for the alpha-chain of human propionyl-CoA carboxylase maps to chromosome band 13q32.

I Kennerknecht1, T Suormala, G Barbi, E R Baumgartner.   

Abstract

The human gene encoding the alpha-polypeptide of propionyl-CoA carboxylase (PCC) has hitherto been localized to the distal half of the long arm of chromosome 13, segment 13q22----q34. We studied the enzyme activities of mitochondrial carboxylases in cell cultures obtained from patients with different deletions of chromosome 13. By setting the PCC activity in normal diploid cell cultures (control group) at 100%, cell cultures with trisomy 13 showed 150% activity. In contrast, one of four patients with partial monosomy 13 had an enzyme activity of only 50%. Thus, by comparative deletion mapping, combined with studies of the gene-dosage effect, we have been able to assign the PCCA gene locus to chromosome band 13q32.

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Year:  1990        PMID: 2265838     DOI: 10.1007/bf00197713

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  4 in total

1.  Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes.

Authors:  A M Lamhonwah; T J Barankiewicz; H F Willard; D J Mahuran; F Quan; R A Gravel
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

2.  Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sample.

Authors:  T Suormala; H Wick; J P Bonjour; E R Baumgartner
Journal:  Clin Chim Acta       Date:  1985-01-30       Impact factor: 3.786

3.  Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups.

Authors:  B Wolf; L E Rosenberg
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808

4.  The large-scale separation of peroxisomes, mitochondria, and lysosomes from the livers of rats injected with triton WR-1339. Improved isolation procedures, automated analysis, biochemical and morphological properties of fractions.

Authors:  F Leighton; B Poole; H Beaufay; P Baudhuin; J W Coffey; S Fowler; C De Duve
Journal:  J Cell Biol       Date:  1968-05       Impact factor: 10.539

  4 in total
  3 in total

1.  Unusual presentation of propionic acidaemia as isolated cardiomyopathy.

Authors:  T M Lee; L J Addonizio; B A Barshop; W K Chung
Journal:  J Inherit Metab Dis       Date:  2009-02-24       Impact factor: 4.982

2.  Mutations participating in interallelic complementation in propionic acidemia.

Authors:  R A Gravel; B R Akerman; A M Lamhonwah; M Loyer; A Léon-del-Rio; I Italiano
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

3.  Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia.

Authors:  Mohamed H Al-Hamed; Faiqa Imtiaz; Zuhair Al-Hassnan; Mohammed Al-Owain; Hamad Al-Zaidan; Mohamed S Alamoudi; Eissa Faqeih; Majid Alfadhel; Ali Al-Asmari; M M Saleh; Fuad Almutairi; Nabil Moghrabi; Moeenaldeen AlSayed
Journal:  Mol Genet Metab Rep       Date:  2019-01-09
  3 in total

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