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Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi
BACKGROUND: GC-skews have previously been linked to transcription in some eukaryotes. They have been associated with transcription start sites, with the coding strand G-biased in mammals and C-biased in fungi and invertebrates. RESULTS: We show a consistent and highly significant pattern of GC-skew...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315797/ https://www.ncbi.nlm.nih.gov/pubmed/22208287 http://dx.doi.org/10.1186/1471-2164-12-638 |
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author | McLean, Malcolm A Tirosh, Itay |
author_facet | McLean, Malcolm A Tirosh, Itay |
author_sort | McLean, Malcolm A |
collection | PubMed |
description | BACKGROUND: GC-skews have previously been linked to transcription in some eukaryotes. They have been associated with transcription start sites, with the coding strand G-biased in mammals and C-biased in fungi and invertebrates. RESULTS: We show a consistent and highly significant pattern of GC-skew within genes of almost all unicellular fungi. The pattern of GC-skew is asymmetrical: the coding strand of genes is typically C-biased at the 5' ends but G-biased at the 3' ends, with intermediate skews at the middle of genes. Thus, the initiation, elongation, and termination phases of transcription are associated with different skews. This pattern influences the encoded proteins by generating differential usage of amino acids at the 5' and 3' ends of genes. These biases also affect fourfold-degenerate positions and extend into promoters and 3' UTRs, indicating that skews cannot be accounted by selection for protein function or translation. CONCLUSIONS: We propose two explanations, the mutational pressure hypothesis, and the adaptive hypothesis. The mutational pressure hypothesis is that different co-factors bind to RNA pol II at different phases of transcription, producing different mutational regimes. The adaptive hypothesis is that cytidine triphosphate deficiency may lead to C-avoidance at the 3' ends of transcripts to control the flow of RNA pol II molecules and reduce their frequency of collisions. |
format | Online Article Text |
id | pubmed-3315797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33157972012-03-31 Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi McLean, Malcolm A Tirosh, Itay BMC Genomics Research Article BACKGROUND: GC-skews have previously been linked to transcription in some eukaryotes. They have been associated with transcription start sites, with the coding strand G-biased in mammals and C-biased in fungi and invertebrates. RESULTS: We show a consistent and highly significant pattern of GC-skew within genes of almost all unicellular fungi. The pattern of GC-skew is asymmetrical: the coding strand of genes is typically C-biased at the 5' ends but G-biased at the 3' ends, with intermediate skews at the middle of genes. Thus, the initiation, elongation, and termination phases of transcription are associated with different skews. This pattern influences the encoded proteins by generating differential usage of amino acids at the 5' and 3' ends of genes. These biases also affect fourfold-degenerate positions and extend into promoters and 3' UTRs, indicating that skews cannot be accounted by selection for protein function or translation. CONCLUSIONS: We propose two explanations, the mutational pressure hypothesis, and the adaptive hypothesis. The mutational pressure hypothesis is that different co-factors bind to RNA pol II at different phases of transcription, producing different mutational regimes. The adaptive hypothesis is that cytidine triphosphate deficiency may lead to C-avoidance at the 3' ends of transcripts to control the flow of RNA pol II molecules and reduce their frequency of collisions. BioMed Central 2011-12-30 /pmc/articles/PMC3315797/ /pubmed/22208287 http://dx.doi.org/10.1186/1471-2164-12-638 Text en Copyright ©2011 McLean and Tirosh; 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 | Research Article McLean, Malcolm A Tirosh, Itay Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
title | Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
title_full | Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
title_fullStr | Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
title_full_unstemmed | Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
title_short | Opposite GC skews at the 5' and 3' ends of genes in unicellular fungi |
title_sort | opposite gc skews at the 5' and 3' ends of genes in unicellular fungi |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315797/ https://www.ncbi.nlm.nih.gov/pubmed/22208287 http://dx.doi.org/10.1186/1471-2164-12-638 |
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