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Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast

BACKGROUND: More than two thirds of the highly expressed ribosomal protein (RP) genes in Saccharomyces cerevisiae contain introns, which is in sharp contrast to the genome-wide five percent intron-containing genes. It is well established that introns carry regulatory sequences and that the transcrip...

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Autores principales: Zhang, Jing, Vingron, Martin, Roepcke, Stefan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2585575/
https://www.ncbi.nlm.nih.gov/pubmed/18959800
http://dx.doi.org/10.1186/1756-0500-1-109
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author Zhang, Jing
Vingron, Martin
Roepcke, Stefan
author_facet Zhang, Jing
Vingron, Martin
Roepcke, Stefan
author_sort Zhang, Jing
collection PubMed
description BACKGROUND: More than two thirds of the highly expressed ribosomal protein (RP) genes in Saccharomyces cerevisiae contain introns, which is in sharp contrast to the genome-wide five percent intron-containing genes. It is well established that introns carry regulatory sequences and that the transcription of RP genes is extensively and coordinately regulated. Here we test the hypotheses that introns are innately associated with heavily transcribed genes and that introns of RP genes contribute regulatory TF binding sequences. Moreover, we investigate whether promoter features are significantly different between intron-containing and intronless RP genes. RESULTS: We find that directly measured transcription rates tend to be lower for intron-containing compared to intronless RP genes. We do not observe any specifically enriched sequence motifs in the introns of RP genes other than those of the branch point and the two splice sites. Comparing the promoters of intron-containing and intronless RP genes, we detect differences in number and position of Rap1-binding and IFHL motifs. Moreover, the analysis of the length distribution and the folding free energies suggest that, at least in a sub-population of RP genes, the 5' untranslated sequences are optimized for regulatory function. CONCLUSION: Our results argue against the direct involvement of introns in the regulation of transcription of highly expressed genes. Moreover, systematic differences in motif distributions suggest that RP transcription factors may act differently on intron-containing and intronless gene promoters. Thus, our findings contribute to the decoding of the RP promoter architecture and may fuel the discussion on the evolution of introns.
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spelling pubmed-25855752008-11-21 Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast Zhang, Jing Vingron, Martin Roepcke, Stefan BMC Res Notes Short Report BACKGROUND: More than two thirds of the highly expressed ribosomal protein (RP) genes in Saccharomyces cerevisiae contain introns, which is in sharp contrast to the genome-wide five percent intron-containing genes. It is well established that introns carry regulatory sequences and that the transcription of RP genes is extensively and coordinately regulated. Here we test the hypotheses that introns are innately associated with heavily transcribed genes and that introns of RP genes contribute regulatory TF binding sequences. Moreover, we investigate whether promoter features are significantly different between intron-containing and intronless RP genes. RESULTS: We find that directly measured transcription rates tend to be lower for intron-containing compared to intronless RP genes. We do not observe any specifically enriched sequence motifs in the introns of RP genes other than those of the branch point and the two splice sites. Comparing the promoters of intron-containing and intronless RP genes, we detect differences in number and position of Rap1-binding and IFHL motifs. Moreover, the analysis of the length distribution and the folding free energies suggest that, at least in a sub-population of RP genes, the 5' untranslated sequences are optimized for regulatory function. CONCLUSION: Our results argue against the direct involvement of introns in the regulation of transcription of highly expressed genes. Moreover, systematic differences in motif distributions suggest that RP transcription factors may act differently on intron-containing and intronless gene promoters. Thus, our findings contribute to the decoding of the RP promoter architecture and may fuel the discussion on the evolution of introns. BioMed Central 2008-10-29 /pmc/articles/PMC2585575/ /pubmed/18959800 http://dx.doi.org/10.1186/1756-0500-1-109 Text en Copyright © 2008 Roepcke et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Zhang, Jing
Vingron, Martin
Roepcke, Stefan
Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
title Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
title_full Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
title_fullStr Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
title_full_unstemmed Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
title_short Characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
title_sort characteristic differences between the promoters of intron-containing and intronless ribosomal protein genes in yeast
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2585575/
https://www.ncbi.nlm.nih.gov/pubmed/18959800
http://dx.doi.org/10.1186/1756-0500-1-109
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