Cargando…

Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator

Core promoters and chromatin insulators are key regulatory elements that may direct a transcriptional enhancer to prefer a specific promoter in complex genetic loci. Enhancer and insulator flank the sea urchin (Paracentrotus lividus) α-histone H2A transcription unit in a tandem repeated cluster cont...

Descripción completa

Detalles Bibliográficos
Autores principales: Cavalieri, Vincenzo, Melfi, Raffaella, Spinelli, Giovanni
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794192/
https://www.ncbi.nlm.nih.gov/pubmed/19843609
http://dx.doi.org/10.1093/nar/gkp859
_version_ 1782175359583649792
author Cavalieri, Vincenzo
Melfi, Raffaella
Spinelli, Giovanni
author_facet Cavalieri, Vincenzo
Melfi, Raffaella
Spinelli, Giovanni
author_sort Cavalieri, Vincenzo
collection PubMed
description Core promoters and chromatin insulators are key regulatory elements that may direct a transcriptional enhancer to prefer a specific promoter in complex genetic loci. Enhancer and insulator flank the sea urchin (Paracentrotus lividus) α-histone H2A transcription unit in a tandem repeated cluster containing the five histone genes. This article deals with the specificity of interaction between the H2A enhancer-bound MBF-1 activator and histone gene promoters, and with the mechanism that leads the H1 transcripts to peak at about one-third of the value for nucleosomal H3 and H2A mRNAs. To this end, in vivo competition assays of enhancer and insulator functions were performed. Our evidence suggests that the MBF-1 transcription factor participates also in the expression of the H3 gene and that the sns5 insulator buffers the downstream H1 promoter from the H2A enhancer. Altogether, these results provide a clear demonstration of the enhancer-blocking function of a chromatin insulator in a natural gene context. In addition, they suggest that both the H2A enhancer and the sns5 insulator may account for the diverse accumulation of the linker H1 versus the core nucleosomal histones during early development of the sea urchin embryo.
format Text
id pubmed-2794192
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-27941922009-12-16 Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator Cavalieri, Vincenzo Melfi, Raffaella Spinelli, Giovanni Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Core promoters and chromatin insulators are key regulatory elements that may direct a transcriptional enhancer to prefer a specific promoter in complex genetic loci. Enhancer and insulator flank the sea urchin (Paracentrotus lividus) α-histone H2A transcription unit in a tandem repeated cluster containing the five histone genes. This article deals with the specificity of interaction between the H2A enhancer-bound MBF-1 activator and histone gene promoters, and with the mechanism that leads the H1 transcripts to peak at about one-third of the value for nucleosomal H3 and H2A mRNAs. To this end, in vivo competition assays of enhancer and insulator functions were performed. Our evidence suggests that the MBF-1 transcription factor participates also in the expression of the H3 gene and that the sns5 insulator buffers the downstream H1 promoter from the H2A enhancer. Altogether, these results provide a clear demonstration of the enhancer-blocking function of a chromatin insulator in a natural gene context. In addition, they suggest that both the H2A enhancer and the sns5 insulator may account for the diverse accumulation of the linker H1 versus the core nucleosomal histones during early development of the sea urchin embryo. Oxford University Press 2009-12 2009-10-20 /pmc/articles/PMC2794192/ /pubmed/19843609 http://dx.doi.org/10.1093/nar/gkp859 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/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/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene Regulation, Chromatin and Epigenetics
Cavalieri, Vincenzo
Melfi, Raffaella
Spinelli, Giovanni
Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator
title Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator
title_full Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator
title_fullStr Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator
title_full_unstemmed Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator
title_short Promoter activity of the sea urchin (Paracentrotus lividus) nucleosomal H3 and H2A and linker H1 α-histone genes is modulated by enhancer and chromatin insulator
title_sort promoter activity of the sea urchin (paracentrotus lividus) nucleosomal h3 and h2a and linker h1 α-histone genes is modulated by enhancer and chromatin insulator
topic Gene Regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794192/
https://www.ncbi.nlm.nih.gov/pubmed/19843609
http://dx.doi.org/10.1093/nar/gkp859
work_keys_str_mv AT cavalierivincenzo promoteractivityoftheseaurchinparacentrotuslividusnucleosomalh3andh2aandlinkerh1ahistonegenesismodulatedbyenhancerandchromatininsulator
AT melfiraffaella promoteractivityoftheseaurchinparacentrotuslividusnucleosomalh3andh2aandlinkerh1ahistonegenesismodulatedbyenhancerandchromatininsulator
AT spinelligiovanni promoteractivityoftheseaurchinparacentrotuslividusnucleosomalh3andh2aandlinkerh1ahistonegenesismodulatedbyenhancerandchromatininsulator