Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Dorca-Fornell, Carmen, Pajor, Radoslaw, Lehmeier, Christoph, Pérez-Bueno, Marísa, Bauch, Marion, Sloan, Jen, Osborne, Colin, Rolfe, Stephen, Sturrock, Craig, Mooney, Sacha, Fleming, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2013
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
_version_ 1782351151254994944
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
work_keys_str_mv AT dorcafornellcarmen increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT pajorradoslaw increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT lehmeierchristoph increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT perezbuenomarisa increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT bauchmarion increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT sloanjen increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT osbornecolin increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT rolfestephen increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT sturrockcraig increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT mooneysacha increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern
AT flemingandrew increasedleafmesophyllporosityfollowingtransientretinoblastomarelatedproteinsilencingisrevealedbymicrocomputedtomographyimagingandleadstoasystemlevelphysiologicalresponsetothealteredcelldivisionpattern