Literature DB >> 9531504

Structure of the human hexokinase type I gene and nucleotide sequence of the 5' flanking region.

A Ruzzo1, F Andreoni, M Magnani.   

Abstract

This study reports the precise intron/exon boundaries and intron/exon composition of the human hexokinase type I gene. A yeast artificial chromosome containing the hexokinase type I gene was isolated from the yeast artificial chromosome library of the Centre d'Etude du Polymorphisme Humaine. A cosmid sublibrary was created and direct sequencing of the individual cosmids was used to provide the exon/intron organization. The human hexokinase type I gene was found to be composed of 18 exons ranging in size from 63 to 305 bp. Intron 1 is at least 15 kb in length, whereas intron 2 spans at least 10 kb. Overall, the length of the 17 introns ranges from 104 to greater than 15 kb. The entire coding region is contained in at least 75 kb of the gene. The structure of the gene reveals a remarkable conservation of the size of the exons compared with glucokinase and hexokinase type II. Isolation of the 5' flanking region of the gene revealed a 75-90% identity with the rat sequence. Direct evidence of an alternative red-blood-cell-specific exon 1 located upstream of the 5' flanking region of the gene is also provided.

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Year:  1998        PMID: 9531504      PMCID: PMC1219395          DOI: 10.1042/bj3310607

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  52 in total

1.  Structural analysis of human pyruvate kinase L-gene and identification of the promoter activity in erythroid cells.

Authors:  H Kanno; H Fujii; S Miwa
Journal:  Biochem Biophys Res Commun       Date:  1992-10-30       Impact factor: 3.575

2.  Complete amino acid sequence of the type III isozyme of rat hexokinase, deduced from the cloned cDNA.

Authors:  D A Schwab; J E Wilson
Journal:  Arch Biochem Biophys       Date:  1991-03       Impact factor: 4.013

3.  Automated "hot start" PCR using mineral oil and paraffin wax.

Authors:  B J Bassam; G Caetano-Anollés
Journal:  Biotechniques       Date:  1993-01       Impact factor: 1.993

4.  Mammalian hexokinase 1: evolutionary conservation and structure to function analysis.

Authors:  L D Griffin; B D Gelb; D A Wheeler; D Davison; V Adams; E R McCabe
Journal:  Genomics       Date:  1991-12       Impact factor: 5.736

5.  Human glucokinase gene: isolation, structural characterization, and identification of a microsatellite repeat polymorphism.

Authors:  Y Tanizawa; A Matsutani; K C Chiu; M A Permutt
Journal:  Mol Endocrinol       Date:  1992-07

6.  Functional consequences of mutation of highly conserved serine residues, found at equivalent positions in the N- and C-terminal domains of mammalian hexokinases.

Authors:  M Baijal; J E Wilson
Journal:  Arch Biochem Biophys       Date:  1992-10       Impact factor: 4.013

7.  In vitro and in vivo protein--DNA interactions on the rat erythroid-specific L' pyruvate kinase gene promoter.

Authors:  V Lacronique; D Boquet; S Lopez; A Kahn; M Raymondjean
Journal:  Nucleic Acids Res       Date:  1992-11-11       Impact factor: 16.971

8.  Complete amino acid sequence of the type II isozyme of rat hexokinase, deduced from the cloned cDNA: comparison with a hexokinase from novikoff ascites tumor.

Authors:  A P Thelen; J E Wilson
Journal:  Arch Biochem Biophys       Date:  1991-05-01       Impact factor: 4.013

9.  Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.

Authors:  M Stoffel; P Froguel; J Takeda; H Zouali; N Vionnet; S Nishi; I T Weber; R W Harrison; S J Pilkis; S Lesage
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

10.  A single mRNA, transcribed from an alternative, erythroid-specific, promoter, codes for two non-myristylated forms of NADH-cytochrome b5 reductase.

Authors:  G Pietrini; D Aggujaro; P Carrera; J Malyszko; A Vitale; N Borgese
Journal:  J Cell Biol       Date:  1992-06       Impact factor: 10.539

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  4 in total

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2.  First mutation in the red blood cell-specific promoter of hexokinase combined with a novel missense mutation causes hexokinase deficiency and mild chronic hemolysis.

Authors:  Karen M K de Vooght; Wouter W van Solinge; Annet C van Wesel; Sabina Kersting; Richard van Wijk
Journal:  Haematologica       Date:  2009-07-16       Impact factor: 9.941

3.  A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR).

Authors:  Janina Hantke; David Chandler; Rosalind King; Ronald J A Wanders; Dora Angelicheva; Ivailo Tournev; Elyshia McNamara; Marcel Kwa; Velina Guergueltcheva; Radka Kaneva; Frank Baas; Luba Kalaydjieva
Journal:  Eur J Hum Genet       Date:  2009-06-17       Impact factor: 4.246

4.  PharmGKB summary: methylene blue pathway.

Authors:  Ellen M McDonagh; José M Bautista; Ilan Youngster; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2013-09       Impact factor: 2.089

  4 in total

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