Literature DB >> 8468053

Structural organization of the human isovaleryl-CoA dehydrogenase gene.

B Parimoo1, K Tanaka.   

Abstract

Isovaleryl-CoA dehydrogenase (IVD) catalyzes the third step in leucine catabolism. The genetic deficiency of IVD causes isovaleric acidemia. The functional IVD gene spans approximately 15 kb and consists of 12 exons and 11 introns, with the exon size ranging from 52 to 728 bp. The poly(A) addition site begins 21 nucleotides downstream of this signal. The 5'-flanking region contained typical promoter elements such as TATA and CAT boxes in addition to other putative regulatory sequences. The transcription start site appeared to be located 344 bp upstream of the initiator methionine codon. The GC content in this region is very high. In Northern blot analysis, the IVD cDNA probe hybridized to three RNA species of sizes 2.1, 3.6, and 4.8 kb, respectively. The 2.1-kb band corresponds to the size of IVD cDNA. The results from experiments using an IVD-specific oligomer and stringent washes with 3.0 M tetramethylammonium chloride suggested that high GC content may have caused hybridization of the probe to the 3.6- and 4.8-kb species.

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Year:  1993        PMID: 8468053     DOI: 10.1006/geno.1993.1111

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  8 in total

Review 1.  Newborn screening: After the thrill is gone.

Authors:  Jerry Vockley
Journal:  Mol Genet Metab       Date:  2007-07-02       Impact factor: 4.797

2.  Chronic intermittent form of isovaleric aciduria in a 2-year-old boy.

Authors:  Jin Min Cho; Beom Hee Lee; Gu-Hwan Kim; Yoo-Mi Kim; Jin-Ho Choi; Han-Wook Yoo
Journal:  Korean J Pediatr       Date:  2013-08-27

3.  Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia.

Authors:  María L Couce; Luís Aldamiz-Echevarría; María A Bueno; Patricia Barros; Amaya Belanger-Quintana; Javier Blasco; María-Teresa García-Silva; Ana M Márquez-Armenteros; Isidro Vitoria; Inmaculada Vives; Rosa Navarrete; Ana Fernández-Marmiesse; Belén Pérez; Celia Pérez-Cerdá
Journal:  J Hum Genet       Date:  2016-12-01       Impact factor: 3.172

4.  Structural organization of the human short-chain acyl-CoA dehydrogenase gene.

Authors:  M J Corydon; B S Andresen; P Bross; M Kjeldsen; P H Andreasen; H Eiberg; S Kølvraa; N Gregersen
Journal:  Mamm Genome       Date:  1997-12       Impact factor: 2.957

5.  Exon skipping in IVD RNA processing in isovaleric acidemia caused by point mutations in the coding region of the IVD gene.

Authors:  J Vockley; P K Rogan; B D Anderson; J Willard; R S Seelan; D I Smith; W Liu
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

Review 6.  Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneity.

Authors:  Jerry Vockley; Regina Ensenauer
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-05-15       Impact factor: 3.908

7.  Characterization of variants of uncertain significance in isovaleryl-CoA dehydrogenase identified through newborn screening: An approach for faster analysis.

Authors:  Olivia M D'Annibale; Erik A Koppes; Ahmad N Alodaib; Catherine Kochersperger; Anuradha Karunanidhi; Al-Walid Mohsen; Jerry Vockley
Journal:  Mol Genet Metab       Date:  2021-08-30       Impact factor: 4.204

8.  A common mutation is associated with a mild, potentially asymptomatic phenotype in patients with isovaleric acidemia diagnosed by newborn screening.

Authors:  Regina Ensenauer; Jerry Vockley; Jan-Marie Willard; Joseph C Huey; Jörn Oliver Sass; Steven D Edland; Barbara K Burton; Susan A Berry; René Santer; Sarah Grünert; Hans-Georg Koch; Iris Marquardt; Piero Rinaldo; Sihoun Hahn; Dietrich Matern
Journal:  Am J Hum Genet       Date:  2004-10-14       Impact factor: 11.025

  8 in total

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