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Molecular analysis of SCARECROW genes expressed in white lupin cluster roots
The Scarecrow (SCR) transcription factor plays a crucial role in root cell radial patterning and is required for maintenance of the quiescent centre and differentiation of the endodermis. In response to phosphorus (P) deficiency, white lupin (Lupinus albus L.) root surface area increases some 50-fol...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837254/ https://www.ncbi.nlm.nih.gov/pubmed/20167612 http://dx.doi.org/10.1093/jxb/erp400 |
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author | Sbabou, Laila Bucciarelli, Bruna Miller, Susan Liu, Junqi Berhada, Fatiha Filali-Maltouf, Abdelkarim Allan, Deborah Vance, Carroll |
author_facet | Sbabou, Laila Bucciarelli, Bruna Miller, Susan Liu, Junqi Berhada, Fatiha Filali-Maltouf, Abdelkarim Allan, Deborah Vance, Carroll |
author_sort | Sbabou, Laila |
collection | PubMed |
description | The Scarecrow (SCR) transcription factor plays a crucial role in root cell radial patterning and is required for maintenance of the quiescent centre and differentiation of the endodermis. In response to phosphorus (P) deficiency, white lupin (Lupinus albus L.) root surface area increases some 50-fold to 70-fold due to the development of cluster (proteoid) roots. Previously it was reported that SCR-like expressed sequence tags (ESTs) were expressed during early cluster root development. Here the cloning of two white lupin SCR genes, LaSCR1 and LaSCR2, is reported. The predicted amino acid sequences of both LaSCR gene products are highly similar to AtSCR and contain C-terminal conserved GRAS family domains. LaSCR1 and LaSCR2 transcript accumulation localized to the endodermis of both normal and cluster roots as shown by in situ hybridization and gene promoter::reporter staining. Transcript analysis as evaluated by quantitative real-time-PCR (qRT-PCR) and RNA gel hybridization indicated that the two LaSCR genes are expressed predominantly in roots. Expression of LaSCR genes was not directly responsive to the P status of the plant but was a function of cluster root development. Suppression of LaSCR1 in transformed roots of lupin and Medicago via RNAi (RNA interference) delivered through Agrobacterium rhizogenes resulted in decreased root numbers, reflecting the potential role of LaSCR1 in maintaining root growth in these species. The results suggest that the functional orthologues of AtSCR have been characterized. |
format | Text |
id | pubmed-2837254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28372542010-03-15 Molecular analysis of SCARECROW genes expressed in white lupin cluster roots Sbabou, Laila Bucciarelli, Bruna Miller, Susan Liu, Junqi Berhada, Fatiha Filali-Maltouf, Abdelkarim Allan, Deborah Vance, Carroll J Exp Bot Research Papers The Scarecrow (SCR) transcription factor plays a crucial role in root cell radial patterning and is required for maintenance of the quiescent centre and differentiation of the endodermis. In response to phosphorus (P) deficiency, white lupin (Lupinus albus L.) root surface area increases some 50-fold to 70-fold due to the development of cluster (proteoid) roots. Previously it was reported that SCR-like expressed sequence tags (ESTs) were expressed during early cluster root development. Here the cloning of two white lupin SCR genes, LaSCR1 and LaSCR2, is reported. The predicted amino acid sequences of both LaSCR gene products are highly similar to AtSCR and contain C-terminal conserved GRAS family domains. LaSCR1 and LaSCR2 transcript accumulation localized to the endodermis of both normal and cluster roots as shown by in situ hybridization and gene promoter::reporter staining. Transcript analysis as evaluated by quantitative real-time-PCR (qRT-PCR) and RNA gel hybridization indicated that the two LaSCR genes are expressed predominantly in roots. Expression of LaSCR genes was not directly responsive to the P status of the plant but was a function of cluster root development. Suppression of LaSCR1 in transformed roots of lupin and Medicago via RNAi (RNA interference) delivered through Agrobacterium rhizogenes resulted in decreased root numbers, reflecting the potential role of LaSCR1 in maintaining root growth in these species. The results suggest that the functional orthologues of AtSCR have been characterized. Oxford University Press 2010-03 2010-02-18 /pmc/articles/PMC2837254/ /pubmed/20167612 http://dx.doi.org/10.1093/jxb/erp400 Text en © 2010 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details) |
spellingShingle | Research Papers Sbabou, Laila Bucciarelli, Bruna Miller, Susan Liu, Junqi Berhada, Fatiha Filali-Maltouf, Abdelkarim Allan, Deborah Vance, Carroll Molecular analysis of SCARECROW genes expressed in white lupin cluster roots |
title | Molecular analysis of SCARECROW genes expressed in white lupin cluster roots |
title_full | Molecular analysis of SCARECROW genes expressed in white lupin cluster roots |
title_fullStr | Molecular analysis of SCARECROW genes expressed in white lupin cluster roots |
title_full_unstemmed | Molecular analysis of SCARECROW genes expressed in white lupin cluster roots |
title_short | Molecular analysis of SCARECROW genes expressed in white lupin cluster roots |
title_sort | molecular analysis of scarecrow genes expressed in white lupin cluster roots |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837254/ https://www.ncbi.nlm.nih.gov/pubmed/20167612 http://dx.doi.org/10.1093/jxb/erp400 |
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