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Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis
Mammalian promoters are categorized into TATA and CpG-related groups, and they have complementary roles associated with differentiated transcriptional characteristics. While the TATA box is also found in plant promoters, it is not known if CpG-type promoters exist in plants. Plant promoters contain...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2094075/ https://www.ncbi.nlm.nih.gov/pubmed/17855401 http://dx.doi.org/10.1093/nar/gkm685 |
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author | Yamamoto, Yoshiharu Y. Ichida, Hiroyuki Abe, Tomoko Suzuki, Yutaka Sugano, Sumio Obokata, Junichi |
author_facet | Yamamoto, Yoshiharu Y. Ichida, Hiroyuki Abe, Tomoko Suzuki, Yutaka Sugano, Sumio Obokata, Junichi |
author_sort | Yamamoto, Yoshiharu Y. |
collection | PubMed |
description | Mammalian promoters are categorized into TATA and CpG-related groups, and they have complementary roles associated with differentiated transcriptional characteristics. While the TATA box is also found in plant promoters, it is not known if CpG-type promoters exist in plants. Plant promoters contain Y Patches (pyrimidine patches) in the core promoter region, and the ubiquity of these beyond higher plants is not understood as well. Sets of promoter sequences were utilized for the analysis of local distribution of short sequences (LDSS), and approximately one thousand octamer sequences have been identified as promoter constituents from Arabidopsis, rice, human and mouse, respectively. Based on their localization profiles, the identified octamer sequences were classified into several major groups, REG (Regulatory Element Group), TATA box, Inr (Initiator), Kozak, CpG and Y Patch. Comparison of the four species has revealed three categories: (i) shared groups found in both plants and mammals (TATA box), (ii) common groups found in both kingdoms but the utilized sequence is differentiated (REG, Inr and Kozak) and (iii) specific groups found in either plants or mammals (CpG and Y Patch). Our comparative LDSS analysis has identified conservation and differentiation of promoter architectures between higher plants and mammals. |
format | Text |
id | pubmed-2094075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20940752007-12-03 Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis Yamamoto, Yoshiharu Y. Ichida, Hiroyuki Abe, Tomoko Suzuki, Yutaka Sugano, Sumio Obokata, Junichi Nucleic Acids Res Genomics Mammalian promoters are categorized into TATA and CpG-related groups, and they have complementary roles associated with differentiated transcriptional characteristics. While the TATA box is also found in plant promoters, it is not known if CpG-type promoters exist in plants. Plant promoters contain Y Patches (pyrimidine patches) in the core promoter region, and the ubiquity of these beyond higher plants is not understood as well. Sets of promoter sequences were utilized for the analysis of local distribution of short sequences (LDSS), and approximately one thousand octamer sequences have been identified as promoter constituents from Arabidopsis, rice, human and mouse, respectively. Based on their localization profiles, the identified octamer sequences were classified into several major groups, REG (Regulatory Element Group), TATA box, Inr (Initiator), Kozak, CpG and Y Patch. Comparison of the four species has revealed three categories: (i) shared groups found in both plants and mammals (TATA box), (ii) common groups found in both kingdoms but the utilized sequence is differentiated (REG, Inr and Kozak) and (iii) specific groups found in either plants or mammals (CpG and Y Patch). Our comparative LDSS analysis has identified conservation and differentiation of promoter architectures between higher plants and mammals. Oxford University Press 2007-09 2007-09-12 /pmc/articles/PMC2094075/ /pubmed/17855401 http://dx.doi.org/10.1093/nar/gkm685 Text en © 2007 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 | Genomics Yamamoto, Yoshiharu Y. Ichida, Hiroyuki Abe, Tomoko Suzuki, Yutaka Sugano, Sumio Obokata, Junichi Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis |
title | Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis |
title_full | Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis |
title_fullStr | Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis |
title_full_unstemmed | Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis |
title_short | Differentiation of core promoter architecture between plants and mammals revealed by LDSS analysis |
title_sort | differentiation of core promoter architecture between plants and mammals revealed by ldss analysis |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2094075/ https://www.ncbi.nlm.nih.gov/pubmed/17855401 http://dx.doi.org/10.1093/nar/gkm685 |
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