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Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern
The causal relationship between cell division and growth in plants is complex. Although altered expression of cell-cycle genes frequently leads to altered organ growth, there are many examples where manipulation of the division machinery leads to a limited outcome at the level of organ form, despite...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282533/ https://www.ncbi.nlm.nih.gov/pubmed/24118480 http://dx.doi.org/10.1111/tpj.12342 |
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author | Dorca-Fornell, Carmen Pajor, Radoslaw Lehmeier, Christoph Pérez-Bueno, Marísa Bauch, Marion Sloan, Jen Osborne, Colin Rolfe, Stephen Sturrock, Craig Mooney, Sacha Fleming, Andrew |
author_facet | Dorca-Fornell, Carmen Pajor, Radoslaw Lehmeier, Christoph Pérez-Bueno, Marísa Bauch, Marion Sloan, Jen Osborne, Colin Rolfe, Stephen Sturrock, Craig Mooney, Sacha Fleming, Andrew |
author_sort | Dorca-Fornell, Carmen |
collection | PubMed |
description | The causal relationship between cell division and growth in plants is complex. Although altered expression of cell-cycle genes frequently leads to altered organ growth, there are many examples where manipulation of the division machinery leads to a limited outcome at the level of organ form, despite changes in constituent cell size. One possibility, which has been under-explored, is that altered division patterns resulting from manipulation of cell-cycle gene expression alter the physiology of the organ, and that this has an effect on growth. We performed a series of experiments on retinoblastoma-related protein (RBR), a well characterized regulator of the cell cycle, to investigate the outcome of altered cell division on leaf physiology. Our approach involved combination of high-resolution microCT imaging and physiological analysis with a transient gene induction system, providing a powerful approach for the study of developmental physiology. Our investigation identifies a new role for RBR in mesophyll differentiation that affects tissue porosity and the distribution of air space within the leaf. The data demonstrate the importance of RBR in early leaf development and the extent to which physiology adapts to modified cellular architecture resulting from altered cell-cycle gene expression. |
format | Online Article Text |
id | pubmed-4282533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42825332015-01-15 Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern Dorca-Fornell, Carmen Pajor, Radoslaw Lehmeier, Christoph Pérez-Bueno, Marísa Bauch, Marion Sloan, Jen Osborne, Colin Rolfe, Stephen Sturrock, Craig Mooney, Sacha Fleming, Andrew Plant J Original Articles The causal relationship between cell division and growth in plants is complex. Although altered expression of cell-cycle genes frequently leads to altered organ growth, there are many examples where manipulation of the division machinery leads to a limited outcome at the level of organ form, despite changes in constituent cell size. One possibility, which has been under-explored, is that altered division patterns resulting from manipulation of cell-cycle gene expression alter the physiology of the organ, and that this has an effect on growth. We performed a series of experiments on retinoblastoma-related protein (RBR), a well characterized regulator of the cell cycle, to investigate the outcome of altered cell division on leaf physiology. Our approach involved combination of high-resolution microCT imaging and physiological analysis with a transient gene induction system, providing a powerful approach for the study of developmental physiology. Our investigation identifies a new role for RBR in mesophyll differentiation that affects tissue porosity and the distribution of air space within the leaf. The data demonstrate the importance of RBR in early leaf development and the extent to which physiology adapts to modified cellular architecture resulting from altered cell-cycle gene expression. BlackWell Publishing Ltd 2013-12 2013-11-11 /pmc/articles/PMC4282533/ /pubmed/24118480 http://dx.doi.org/10.1111/tpj.12342 Text en © 2013 The Authors The Plant Journal © 2013 John Wiley & Sons Ltd http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Dorca-Fornell, Carmen Pajor, Radoslaw Lehmeier, Christoph Pérez-Bueno, Marísa Bauch, Marion Sloan, Jen Osborne, Colin Rolfe, Stephen Sturrock, Craig Mooney, Sacha Fleming, Andrew Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
title | Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
title_full | Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
title_fullStr | Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
title_full_unstemmed | Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
title_short | Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
title_sort | increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282533/ https://www.ncbi.nlm.nih.gov/pubmed/24118480 http://dx.doi.org/10.1111/tpj.12342 |
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