Skip Navigation



JXB Advance Access published online on November 1, 2004

Journal of Experimental Botany, doi:10.1093/jxb/eri015
© 2004 by Oxford University Press
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary data
Right arrow All Versions of this Article:
56/409/101    most recent
eri015v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
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 PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Moyle, R.
Right arrow Articles by Botella, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Moyle, R.
Right arrow Articles by Botella, J. R.
Agricola
Right arrow Articles by Moyle, R.
Right arrow Articles by Botella, J. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received April 5, 2004
Accepted August 20, 2004

RESEARCH PAPER

Developing pineapple fruit has a small transcriptome dominated by metallothionein

Richard Moyle 1, David J. Fairbairn 1, Jonni Ripi 1, Mark Crowe 2, and Jose R. Botella 1*

1 Plant Genetic Engineering Laboratory, Department of Botany, University of Queensland, QLD 4072, Australia
2 Institute of Molecular Biosciences, University of Queensland, Australia

* To whom correspondence should be addressed.
Jose R. Botella, E-mail: j.botella{at}botany.uq.edu.au


   Abstract

In a first step toward understanding the molecular basis of pineapple fruit development, a sequencing project was initiated to survey a range of expressed sequences from green unripe and yellow ripe fruit tissue. A highly abundant metallothionein transcript was identified during library construction, and was estimated to account for up to 50% of all EST library clones. Library clones with metallothionein subtracted were sequenced, and 408 unripe green and 1140 ripe yellow edited EST clone sequences were retrieved. Clone redundancy was high, with the combined 1548 clone sequences clustering into just 634 contigs comprising 191 consensus sequences and 443 singletons. Half of the EST clone sequences clustered within 13.5% and 9.3% of contigs from green unripe and yellow ripe libraries, respectively, indicating that a small subset of genes dominate the majority of the transcriptome. Furthermore, sequence cluster analysis, northern analysis, and functional classification revealed major differences between genes expressed in the unripe green and ripe yellow fruit tissues. Abundant genes identified from the green fruit include a fruit bromelain and a bromelain inhibitor. Abundant genes identified in the yellow fruit library include a MADS box gene, and several genes normally associated with protein synthesis, including homologues of ribosomal L10 and the translation factors SUI1 and eIF5A. Both the green unripe and yellow ripe libraries contained high proportions of clones associated with oxidative stress responses and the detoxification of free radicals.

Keywords: Ananas comosus; EST; metallothionein; non-climacteric fruit; pineapple; fruit ripening.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Plant Physiol.Home page
L. W. Neuteboom, K. O. Matsumoto, and D. A. Christopher
An Extended AE-Rich N-Terminal Trunk in Secreted Pineapple Cystatin Enhances Inhibition of Fruit Bromelain and Is Posttranslationally Removed during Ripening
Plant Physiology, October 1, 2009; 151(2): 515 - 527.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
T. Xue, X. Li, W. Zhu, C. Wu, G. Yang, and C. Zheng
Cotton metallothionein GhMT3a, a reactive oxygen species scavenger, increased tolerance against abiotic stress in transgenic tobacco and yeast
J. Exp. Bot., January 1, 2009; 60(1): 339 - 349.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
Y. Trusov, W. Zhang, S. M. Assmann, and J. R. Botella
G{gamma}1 + G{gamma}2 != G{beta}: Heterotrimeric G Protein G{gamma}-Deficient Mutants Do Not Recapitulate All Phenotypes of G{beta}-Deficient Mutants
Plant Physiology, June 1, 2008; 147(2): 636 - 649.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
J. Yuan, D. Chen, Y. Ren, X. Zhang, and J. Zhao
Characteristic and Expression Analysis of a Metallothionein Gene, OsMT2b, Down-Regulated by Cytokinin Suggests Functions in Root Development and Seed Embryo Germination of Rice
Plant Physiology, April 1, 2008; 146(4): 1637 - 1650.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
W.-J. Guo, M. Meetam, and P. B. Goldsbrough
Examining the Specific Contributions of Individual Arabidopsis Metallothioneins to Copper Distribution and Metal Tolerance
Plant Physiology, April 1, 2008; 146(4): 1697 - 1706.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
M. Faurobert, C. Mihr, N. Bertin, T. Pawlowski, L. Negroni, N. Sommerer, and M. Causse
Major Proteome Variations Associated with Cherry Tomato Pericarp Development and Ripening
Plant Physiology, March 1, 2007; 143(3): 1327 - 1346.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
R. D. Newcomb, R. N. Crowhurst, A. P. Gleave, E. H.A. Rikkerink, A. C. Allan, L. L. Beuning, J. H. Bowen, E. Gera, K. R. Jamieson, B. J. Janssen, et al.
Analyses of Expressed Sequence Tags from Apple
Plant Physiology, May 1, 2006; 141(1): 147 - 166.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.