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Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein

Hox genes determine anterior–posterior specificity of an animal body. In mammals, these genes map onto four chromosomal loci in a clustered manner, and their expression is regulated in a coordinated manner according to their chromosomal structure. In the present study, we analysed the Hoxb9 promoter...

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Detalles Bibliográficos
Autores principales: Yamagishi, Takumi, Hirose, Shigehisa, Kondo, Takashi
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330229/
https://www.ncbi.nlm.nih.gov/pubmed/18276649
http://dx.doi.org/10.1093/nar/gkm1079
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author Yamagishi, Takumi
Hirose, Shigehisa
Kondo, Takashi
author_facet Yamagishi, Takumi
Hirose, Shigehisa
Kondo, Takashi
author_sort Yamagishi, Takumi
collection PubMed
description Hox genes determine anterior–posterior specificity of an animal body. In mammals, these genes map onto four chromosomal loci in a clustered manner, and their expression is regulated in a coordinated manner according to their chromosomal structure. In the present study, we analysed the Hoxb9 promoter and found that promoter activity in cultured cells is linked to secondary structure formation of promoter DNA. In nuclear extracts, we also detected binding activity specific for secondary-structured DNA. We successfully isolated a candidate gene encoding this specific DNA-binding protein, FBXL10, and demonstrated the effects of the gene product on Hoxb9 promoter activity. Our results suggest that DNA can regulate gene expression by other, non-sequence-specific modes of genetic coding.
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spelling pubmed-23302292008-05-05 Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein Yamagishi, Takumi Hirose, Shigehisa Kondo, Takashi Nucleic Acids Res Molecular Biology Hox genes determine anterior–posterior specificity of an animal body. In mammals, these genes map onto four chromosomal loci in a clustered manner, and their expression is regulated in a coordinated manner according to their chromosomal structure. In the present study, we analysed the Hoxb9 promoter and found that promoter activity in cultured cells is linked to secondary structure formation of promoter DNA. In nuclear extracts, we also detected binding activity specific for secondary-structured DNA. We successfully isolated a candidate gene encoding this specific DNA-binding protein, FBXL10, and demonstrated the effects of the gene product on Hoxb9 promoter activity. Our results suggest that DNA can regulate gene expression by other, non-sequence-specific modes of genetic coding. Oxford University Press 2008-04 2008-02-14 /pmc/articles/PMC2330229/ /pubmed/18276649 http://dx.doi.org/10.1093/nar/gkm1079 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Yamagishi, Takumi
Hirose, Shigehisa
Kondo, Takashi
Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
title Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
title_full Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
title_fullStr Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
title_full_unstemmed Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
title_short Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
title_sort secondary dna structure formation for hoxb9 promoter and identification of its specific binding protein
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330229/
https://www.ncbi.nlm.nih.gov/pubmed/18276649
http://dx.doi.org/10.1093/nar/gkm1079
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