Literature DB >> 11001625

The HFE gene undergoes alternate splicing processes.

A Thénié1, M Orhant, I Gicquel, P Fergelot, J Y Le Gall, V David, J Mosser.   

Abstract

The MHC class I-related HFE gene appears to be involved in iron metabolism, but its pathogenic mechanism in hemochromatosis remains unknown. Furthermore, very little is known about the regulation of its expression. Hybridization of human tissue Northern blots revealed five different HFE mRNAs, indicating that HFE gene transcription is subject to alternative processes. cDNA selection and RT-PCR performed on HeLa cells clearly demonstrated the occurrence of either differential termination or splicing in HFE transcription. Among the numerous molecules identified, two may have a genuine biological significance.

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Year:  2000        PMID: 11001625     DOI: 10.1006/bcmd.2000.0291

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  3 in total

1.  Deletion of murine Smn exon 7 directed to liver leads to severe defect of liver development associated with iron overload.

Authors:  Jérémie M Vitte; Bénédicte Davoult; Natacha Roblot; Michèle Mayer; Vandana Joshi; Sabrina Courageot; François Tronche; Jacqueline Vadrot; Marie Helene Moreau; François Kemeny; Judith Melki
Journal:  Am J Pathol       Date:  2004-11       Impact factor: 4.307

2.  Differential HFE gene expression is regulated by alternative splicing in human tissues.

Authors:  Rute Martins; Bruno Silva; Daniela Proença; Paula Faustino
Journal:  PLoS One       Date:  2011-03-03       Impact factor: 3.240

3.  Alternative polyadenylation and nonsense-mediated decay coordinately regulate the human HFE mRNA levels.

Authors:  Rute Martins; Daniela Proença; Bruno Silva; Cristina Barbosa; Ana Luísa Silva; Paula Faustino; Luísa Romão
Journal:  PLoS One       Date:  2012-04-18       Impact factor: 3.240

  3 in total

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