Plant Physiol. Illumina
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


First published online July 9, 2004; 10.1104/pp.104.041996

Plant Physiology 135:1502-1513 (2004)
© 2004 American Society of Plant Biologists

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
135/3/1502    most recent
pp.104.041996v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (24)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ge, L.
Right arrow Articles by Chong, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ge, L.
Right arrow Articles by Chong, K.
Agricola
Right arrow Articles by Ge, L.
Right arrow Articles by Chong, K.
DEVELOPMENT AND HORMONE ACTION

Overexpression of OsRAA1 Causes Pleiotropic Phenotypes in Transgenic Rice Plants, including Altered Leaf, Flower, and Root Development and Root Response to Gravity1

Lei Ge, Hui Chen, Jia-Fu Jiang, Yuan Zhao, Ming-Li Xu, Yun-Yuan Xu, Ke-hui Tan, Zhi-Hong Xu and Kang Chong*

Research Center for Molecular and Developmental Biology, Key Laboratory of Photosynthesis and Environmental Molecular Physiology, Institute of Botany, The Chinese Academy of Sciences, Beijing 100093, China

There are very few root genes that have been described in rice as a monocotyledonous model plant so far. Here, the OsRAA1 (Oryza sativa Root Architecture Associated 1) gene has been characterized molecularly. OsRAA1 encodes a 12.0-kD protein that has 58% homology to the AtFPF1 (Flowering Promoting Factor 1) in Arabidopsis, which has not been reported as modulating root development yet. Data of in situ hybridization and OsRAA1::GUS transgenic plant showed that OsRAA1 expressed specifically in the apical meristem, the elongation zone of root tip, steles of the branch zone, and the young lateral root. Constitutive expression of OsRAA1 under the control of maize (Zea mays) ubiquitin promoter resulted in phenotypes of reduced growth of primary root, increased number of adventitious roots and helix primary root, and delayed gravitropic response of roots in seedlings of rice (Oryza sativa), which are similar to the phenotypes of the wild-type plant treated with auxin. With overexpression of OsRAA1, initiation and growth of adventitious root were more sensitive to treatment of auxin than those of the control plants, while their responses to 9-hydroxyfluorene-9-carboxylic acid in both transgenic line and wild type showed similar results. OsRAA1 constitutive expression also caused longer leaves and sterile florets at the last stage of plant development. Analysis of northern blot and GUS activity staining of OsRAA1::GUS transgenic plants demonstrated that the OsRAA1 expression was induced by auxin. At the same time, overexpression of OsRAA1 also caused endogenous indole-3-acetic acid to increase. These data suggested that OsRAA1 as a new gene functions in the development of rice root systems, which are mediated by auxin. A positive feedback regulation mechanism of OsRAA1 to indole-3-acetic acid metabolism may be involved in rice root development in nature.


1 This work was supported by the Major State Basic Research Program of China (grant no. G19990116), by the Innovation Grand of CAS, National Nature Science Foundation of China (NSFC; grant no. 30270143), and by the State Project of Transgenic Plant (J99–A–024) as well as the State High-Tech Project (2001AA222281).

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.104.041996.

* Corresponding author; e-mail chongk{at}ibcas.ac.cn; fax 86–10–8259–4821.

Received March 5, 2004; returned for revision April 6, 2004; accepted April 7, 2004.




This article has been cited by other articles:


Home page
Plant Physiol.Home page
Q. Ma, X. Dai, Y. Xu, J. Guo, Y. Liu, N. Chen, J. Xiao, D. Zhang, Z. Xu, X. Zhang, et al.
Enhanced Tolerance to Chilling Stress in OsMYB3R-2 Transgenic Rice Is Mediated by Alteration in Cell Cycle and Ectopic Expression of Stress Genes
Plant Physiology, May 1, 2009; 150(1): 244 - 256.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
Y. Han, H. Cao, J. Jiang, Y. Xu, J. Du, X. Wang, M. Yuan, Z. Wang, Z. Xu, and K. Chong
Rice ROOT ARCHITECTURE ASSOCIATED1 Binds the Proteasome Subunit RPT4 and Is Degraded in a D-Box and Proteasome-Dependent Manner
Plant Physiology, October 1, 2008; 148(2): 843 - 855.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
X. Wang, Y. Xu, Y. Han, S. Bao, J. Du, M. Yuan, Z. Xu, and K. Chong
Overexpression of RAN1 in Rice and Arabidopsis Alters Primordial Meristem, Mitotic Progress, and Sensitivity to Auxin
Plant Physiology, January 1, 2006; 140(1): 91 - 101.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 2004 by the American Society of Plant Biologists