Literature DB >> 10978502

Structure of the 5' region of the human hexokinase type I (HKI) gene and identification of an additional testis-specific HKI mRNA.

F Andreoni1, A Ruzzo, M Magnani.   

Abstract

We previously reported the structure of the human hexokinase type I (HKI) gene and provided direct evidence of an alternative red blood cell-specific exon 1 located in the 5' flanking region of the gene. Three unique HKI mRNA species have also been described in human spermatogenic cells. These mRNAs contain a testis-specific sequence not present in somatic cell HKI, but lack the sequence for the porin-binding domain necessary for HKI to bind to porin on the outer mitochondrial membrane. The present study reports a new mRNA isoform, hHKI-td, isolated from human sperm. hHKI-td mRNA contains both a testis-specific sequence at the 5' end common to the three other mRNA isoforms and an additional unique sequence. Screening of a cosmid library and analysis of the cosmids containing the HKI gene revealed that testis-specific sequences are encoded by six different exons. Five of these exons are located upstream from the somatic exon 1 (5.6-30 kb) and one within intron 1. This study shows that a single human HKI gene spanning at least 100 kb encodes multiple transcripts that are generated by alternative splicing of different 5' exons. Testis-specific transcripts are probably produced by a separate promoter that induces the expression of the HKI gene in spermatogenic cells.

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Year:  2000        PMID: 10978502     DOI: 10.1016/s0167-4781(00)00147-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  6 in total

1.  Bovine hexokinase type I: full-length cDNA sequence and characterisation of the recombinant enzyme.

Authors:  Francesca Andreoni; Giordano Serafini; Maria Elena Laguardia; Mauro Magnani
Journal:  Mol Cell Biochem       Date:  2005-01       Impact factor: 3.396

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.  A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa.

Authors:  Lori S Sullivan; Daniel C Koboldt; Sara J Bowne; Steven Lang; Susan H Blanton; Elizabeth Cadena; Cheryl E Avery; Richard A Lewis; Kaylie Webb-Jones; Dianna H Wheaton; David G Birch; Razck Coussa; Huanan Ren; Irma Lopez; Christina Chakarova; Robert K Koenekoop; Charles A Garcia; Robert S Fulton; Richard K Wilson; George M Weinstock; Stephen P Daiger
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-09-04       Impact factor: 4.799

5.  Costunolide reduces glycolysis-associated activation of hepatic stellate cells via inhibition of hexokinase-2.

Authors:  Dujing Ban; Shangbo Hua; Wen Zhang; Chao Shen; Xuehua Miao; Wensheng Liu
Journal:  Cell Mol Biol Lett       Date:  2019-08-14       Impact factor: 5.787

6.  Novel myristoylation of the sperm-specific hexokinase 1 isoform regulates its atypical localization.

Authors:  Sujeet Kumar; Sreejit Parameswaran; Rajendra K Sharma
Journal:  Biol Open       Date:  2015-11-18       Impact factor: 2.422

  6 in total

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