JXB Advance Access published online on October 17, 2007
Journal of Experimental Botany, doi:10.1093/jxb/erm189
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
FOCUS PAPER |
Programmed cell death and tissue remodeling in plants
Department of Biology, Dalhousie University, Halifax, Nova Scotia, Canada, B3H 4J1
* To whom correspondence should be addressed. E-mail: arunika.gunawardena{at}dal.ca
The use of programmed cell death (PCD) to remodel plants at the cellular, tissue, and organ levels is particularly fascinating and occurs in such processes as tracheary element differentiation, lysigenous aerenchyma formation, development of functionally unisexual flowers from bisexual floral primordia, and leaf morphogenesis. The formation of complex leaf shape through the use of PCD is a rare event across vascular plants and occurs only in a few species of Monstera and related genera, and in the lace plant (Aponogeton madagascariensis). During early development, the lace plant leaf forms a pattern of equidistantly positioned perforations across the surface of the leaf, giving it a lattice-like appearance. Due to the accessibility and predictability of this process, the lace plant provides highly suitable material for the study of developmentally regulated PCD in plants. A sterile lace plant culture system has been successfully established, providing material free of micro-organisms for experimental study. The potential role of ethylene and caspase-like activity in developmentally regulated PCD in the lace plant is currently under investigation, with preliminary results indicating that both may play a role in the cell death pathway.
Key words: Lace plant, leaf morphogenesis, perforations, programmed cell death, remodeling
Received 11 May 2007; Revised 30 June 2007 Accepted 18 July 2007
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
H. Wright, W. G. van Doorn, and A. H. L. A. N. Gunawardena In vivo study of developmental programmed cell death using the lace plant (Aponogeton madagascariensis; Aponogetonaceae) leaf model system Am. J. Botany, May 1, 2009; 96(5): 865 - 876. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. V. Radchuk, L. Borisjuk, N. Sreenivasulu, K. Merx, H.-P. Mock, H. Rolletschek, U. Wobus, and W. Weschke Spatiotemporal Profiling of Starch Biosynthesis and Degradation in the Developing Barley Grain Plant Physiology, May 1, 2009; 150(1): 190 - 204. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Hirano, K. Aya, T. Hobo, H. Sakakibara, M. Kojima, R. A. Shim, Y. Hasegawa, M. Ueguchi-Tanaka, and M. Matsuoka Comprehensive Transcriptome Analysis of Phytohormone Biosynthesis and Signaling Genes in Microspore/Pollen and Tapetum of Rice Plant Cell Physiol., October 1, 2008; 49(10): 1429 - 1450. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Farage-Barhom, S. Burd, L. Sonego, R. Perl-Treves, and A. Lers Expression analysis of the BFN1 nuclease gene promoter during senescence, abscission, and programmed cell death-related processes J. Exp. Bot., September 1, 2008; 59(12): 3247 - 3258. [Abstract] [Full Text] [PDF] |
||||



