Literature DB >> 9530634

Structure of the human biotinidase gene.

H C Knight1, T R Reynolds, G A Meyers, R J Pomponio, G A Buck, B Wolf.   

Abstract

Biotinidase cleaves biotin from biocytin, thereby recycling the vitamin. We have determined the structure of the human biotinidase gene. A genomic clone, containing three exons that code for the mature enzyme, was obtained by screening a human genomic bacteriophage library with the biotinidase cDNA by plaque hybridization. To obtain a clone containing the most 5' exon of the biotinidase cDNA, a human PAC library by PCR was screened. The human biotinidase gene is organized into four exons and spans at least 23 kb. The 5'-flanking region of exon 1 contains a CCAAT element, three initiator sequences, an octamer sequence, three methylation consensus sites, two GC boxes, and one HNF-5 site, but has no TATA element. The region from nt -600 to +400 has features of a CpG island and resembles a housekeeping gene promoter. The structure and sequence of this gene are useful for identifying and characterizing mutations that cause biotinidase deficiency.

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Year:  1998        PMID: 9530634     DOI: 10.1007/s003359900760

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


  19 in total

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Journal:  Nucleic Acids Res       Date:  1989-03-25       Impact factor: 16.971

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Authors:  K J Norrgard; R J Pomponio; K L Swango; J Hymes; T Reynolds; G A Buck; B Wolf
Journal:  Hum Mutat       Date:  1998       Impact factor: 4.878

8.  Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States.

Authors:  K J Norrgard; R J Pomponio; K L Swango; J Hymes; T R Reynolds; G A Buck; B Wolf
Journal:  Biochem Mol Med       Date:  1997-06

9.  Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiency.

Authors:  R J Pomponio; T R Reynolds; H Cole; G A Buck; B Wolf
Journal:  Nat Genet       Date:  1995-09       Impact factor: 38.330

10.  Localization of serum biotinidase (BTD) to human chromosome 3 in band p25.

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Journal:  Genomics       Date:  1994-08       Impact factor: 5.736

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  21 in total

1.  Novel mutations cause biotinidase deficiency in Turkish children.

Authors:  R J Pomponio; T Coskun; M Demirkol; A Tokatli; I Ozalp; G Hüner; T Baykal; B Wolf
Journal:  J Inherit Metab Dis       Date:  2000-03       Impact factor: 4.982

2.  Novel mutations in children with profound biotinidase deficiency from Saudi Arabia.

Authors:  R J Pomponio; P T Ozand; M Al Essa; B Wolf
Journal:  J Inherit Metab Dis       Date:  2000-03       Impact factor: 4.982

3.  Evaluation of the biotinidase activity in hepatic glycogen storage disease patients. Undescribed genetic finding associated with atypical enzymatic behavior: an outlook.

Authors:  Celia J Angaroni; Alicia N Giner-Ayala; Lorena P Hill; Norberto B Guelbert; Ana E Paschini-Capra; Raquel Dodelson de Kremer
Journal:  J Inherit Metab Dis       Date:  2010-06-08       Impact factor: 4.982

4.  Molecular characterisation and neuropsychological outcome of 21 patients with profound biotinidase deficiency detected by newborn screening and family studies.

Authors:  Dorothea Möslinger; Adolf Mühl; Terttu Suormala; Regula Baumgartner; Sylvia Stöckler-Ipsiroglu
Journal:  Eur J Pediatr       Date:  2003-11-20       Impact factor: 3.183

Review 5.  Biological functions of biotinylated histones.

Authors:  Nagarama Kothapalli; Gabriela Camporeale; Alice Kueh; Yap C Chew; Anna M Oommen; Jacob B Griffin; Janos Zempleni
Journal:  J Nutr Biochem       Date:  2005-07       Impact factor: 6.048

6.  Synthetic ecosystems based on airborne inter- and intrakingdom communication.

Authors:  Wilfried Weber; Marie Daoud-El Baba; Martin Fussenegger
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-05       Impact factor: 11.205

7.  Development and characterization of a mouse with profound biotinidase deficiency: a biotin-responsive neurocutaneous disorder.

Authors:  Kirit Pindolia; Megan Jordan; Caiying Guo; Nell Matthews; Donald M Mock; Erin Strovel; Miriam Blitzer; Barry Wolf
Journal:  Mol Genet Metab       Date:  2010-10-13       Impact factor: 4.797

8.  Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screening.

Authors:  Mehmet Karaca; Rıza Köksal Özgül; Özlem Ünal; Didem Yücel-Yılmaz; Mustafa Kılıç; Burcu Hişmi; Ayşegül Tokatlı; Turgay Coşkun; Ali Dursun; Hatice Serap Sivri
Journal:  Eur J Pediatr       Date:  2015-03-11       Impact factor: 3.183

9.  High frequencies of biotinidase (BTD) gene mutations in the Hungarian population.

Authors:  Ilona Milánkovics; Krisztina Németh; Csilla Somogyi; Agnes Schuler; György Fekete
Journal:  J Inherit Metab Dis       Date:  2010-06-15       Impact factor: 4.982

10.  Biotinyl-methyl 4-(amidomethyl)benzoate is a competitive inhibitor of human biotinidase.

Authors:  Keyna A Kobza; Kittichai Chaiseeda; Gautam Sarath; James M Takacs; Janos Zempleni
Journal:  J Nutr Biochem       Date:  2008-05-13       Impact factor: 6.048

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