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Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease

The LEC rat is an authentic model of human Wilson's disease (WD) with an autosomal recessively inherited hepatitis. We investigated linkage between the hepatitis gene (hts) and the rat retinoblas‐toma gene (RB), that is closely linked to the WD gene in humans, to see whether or not the hts gene...

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Autores principales: Sasaki, Nobuya, Hayashizaki, Yoshihide, Kasai, Noriyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919054/
https://www.ncbi.nlm.nih.gov/pubmed/8226276
http://dx.doi.org/10.1111/j.1349-7006.1993.tb02795.x
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author Sasaki, Nobuya
Hayashizaki, Yoshihide
Kasai, Noriyuki
author_facet Sasaki, Nobuya
Hayashizaki, Yoshihide
Kasai, Noriyuki
author_sort Sasaki, Nobuya
collection PubMed
description The LEC rat is an authentic model of human Wilson's disease (WD) with an autosomal recessively inherited hepatitis. We investigated linkage between the hepatitis gene (hts) and the rat retinoblas‐toma gene (RB), that is closely linked to the WD gene in humans, to see whether or not the hts gene is located on the syntenic region of WD and is the counterpart of the WD gene. Polymerase chain reaction‐single strand conformation polymorphism analysis with backcross progenies from LEC and TM strains showed that the recombination rate between these two loci was 55.6%, demonstrating that the hts and RB genes are not linked to each other. These data indicate that the hts gene is not the counterpart of the WD gene and that the human syntenic region on which the WD locus and human RB gene are located, is not conserved in the rat genome.
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spelling pubmed-59190542018-05-11 Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease Sasaki, Nobuya Hayashizaki, Yoshihide Kasai, Noriyuki Jpn J Cancer Res Rapid Communication The LEC rat is an authentic model of human Wilson's disease (WD) with an autosomal recessively inherited hepatitis. We investigated linkage between the hepatitis gene (hts) and the rat retinoblas‐toma gene (RB), that is closely linked to the WD gene in humans, to see whether or not the hts gene is located on the syntenic region of WD and is the counterpart of the WD gene. Polymerase chain reaction‐single strand conformation polymorphism analysis with backcross progenies from LEC and TM strains showed that the recombination rate between these two loci was 55.6%, demonstrating that the hts and RB genes are not linked to each other. These data indicate that the hts gene is not the counterpart of the WD gene and that the human syntenic region on which the WD locus and human RB gene are located, is not conserved in the rat genome. Blackwell Publishing Ltd 1993-10 /pmc/articles/PMC5919054/ /pubmed/8226276 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02795.x Text en
spellingShingle Rapid Communication
Sasaki, Nobuya
Hayashizaki, Yoshihide
Kasai, Noriyuki
Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease
title Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease
title_full Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease
title_fullStr Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease
title_full_unstemmed Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease
title_short Absence of Linkage between the Retinoblastoma Gene and hts Gene in the LEC Rat: A Model of Human Wilson's Disease
title_sort absence of linkage between the retinoblastoma gene and hts gene in the lec rat: a model of human wilson's disease
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919054/
https://www.ncbi.nlm.nih.gov/pubmed/8226276
http://dx.doi.org/10.1111/j.1349-7006.1993.tb02795.x
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