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Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements
BACKGROUND: Much of the organismal variation we observe in nature is due to differences in organ size. The observation that even closely related species can show large, stably inherited differences in organ size indicates a strong genetic component to the control of organ size. Despite recent progre...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362746/ https://www.ncbi.nlm.nih.gov/pubmed/22433627 http://dx.doi.org/10.1186/1471-2229-12-41 |
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author | Breuninger, Holger Lenhard, Michael |
author_facet | Breuninger, Holger Lenhard, Michael |
author_sort | Breuninger, Holger |
collection | PubMed |
description | BACKGROUND: Much of the organismal variation we observe in nature is due to differences in organ size. The observation that even closely related species can show large, stably inherited differences in organ size indicates a strong genetic component to the control of organ size. Despite recent progress in identifying factors controlling organ growth in plants, our overall understanding of this process remains limited, partly because the individual factors have not yet been connected into larger regulatory pathways or networks. To begin addressing this aim, we have studied the upstream regulation of expression of BIG BROTHER (BB), a central growth-control gene in Arabidopsis thaliana that prevents overgrowth of organs. Final organ size and BB expression levels are tightly correlated, implying the need for precise control of its expression. BB expression mirrors proliferative activity, yet the gene functions to limit proliferation, suggesting that it acts in an incoherent feedforward loop downstream of growth activators to prevent over-proliferation. RESULTS: To investigate the upstream regulation of BB we combined a promoter deletion analysis with a phylogenetic footprinting approach. We were able to narrow down important, highly conserved, cis-regulatory elements within the BB promoter. Promoter sequences of other Brassicaceae species were able to partially complement the A. thaliana bb-1 mutant, suggesting that at least within the Brassicaceae family the regulatory pathways are conserved. CONCLUSIONS: This work underlines the complexity involved in precise quantitative control of gene expression and lays the foundation for identifying important upstream regulators that determine BB expression levels and thus final organ size. |
format | Online Article Text |
id | pubmed-3362746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33627462012-05-31 Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements Breuninger, Holger Lenhard, Michael BMC Plant Biol Research Article BACKGROUND: Much of the organismal variation we observe in nature is due to differences in organ size. The observation that even closely related species can show large, stably inherited differences in organ size indicates a strong genetic component to the control of organ size. Despite recent progress in identifying factors controlling organ growth in plants, our overall understanding of this process remains limited, partly because the individual factors have not yet been connected into larger regulatory pathways or networks. To begin addressing this aim, we have studied the upstream regulation of expression of BIG BROTHER (BB), a central growth-control gene in Arabidopsis thaliana that prevents overgrowth of organs. Final organ size and BB expression levels are tightly correlated, implying the need for precise control of its expression. BB expression mirrors proliferative activity, yet the gene functions to limit proliferation, suggesting that it acts in an incoherent feedforward loop downstream of growth activators to prevent over-proliferation. RESULTS: To investigate the upstream regulation of BB we combined a promoter deletion analysis with a phylogenetic footprinting approach. We were able to narrow down important, highly conserved, cis-regulatory elements within the BB promoter. Promoter sequences of other Brassicaceae species were able to partially complement the A. thaliana bb-1 mutant, suggesting that at least within the Brassicaceae family the regulatory pathways are conserved. CONCLUSIONS: This work underlines the complexity involved in precise quantitative control of gene expression and lays the foundation for identifying important upstream regulators that determine BB expression levels and thus final organ size. BioMed Central 2012-03-20 /pmc/articles/PMC3362746/ /pubmed/22433627 http://dx.doi.org/10.1186/1471-2229-12-41 Text en Copyright ©2012 Breuninger and Lenhard; 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 Breuninger, Holger Lenhard, Michael Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements |
title | Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements |
title_full | Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements |
title_fullStr | Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements |
title_full_unstemmed | Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements |
title_short | Expression of the central growth regulator BIG BROTHER is regulated by multiple cis-elements |
title_sort | expression of the central growth regulator big brother is regulated by multiple cis-elements |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362746/ https://www.ncbi.nlm.nih.gov/pubmed/22433627 http://dx.doi.org/10.1186/1471-2229-12-41 |
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