Phytocalpain controls the proliferation and differentiation fates of cells in plant organ development

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Title
Phytocalpain controls the proliferation and differentiation fates of cells in plant organ development
Author(s)
Joon Woo Ahn; Moonil Kim; Jeong Hwa Lim; G T Kim; H S Pai
Bibliographic Citation
Plant Journal, vol. 38, no. 6, pp. 969-981
Publication Year
2004
Abstract
Calpain, a calcium-dependent cysteine protease, plays an essential role in basic cellular processes in animal cells, including cell proliferation, apoptosis, and differentiation. NbDEK encodes the calpain homolog of N. benthamiana. In this study, virus-induced gene silencing (VIGS) of NbDEK resulted in arrested organ development and hyperplasia in all the major plant organs examined. The epidermal layers of the leaves and stems were covered with hyperproliferating cell masses, and stomata and trichome development was severely inhibited. During flower development, a single dome-like structure was grown from the flower meristem to generate a large cylinder-shaped flower lacking any floral organs. At the cellular level, cell division was sustained in tissues that were otherwise already differentiated, and cell differentiation was severely hampered. NbDEK is ubiquitously expressed in all the plant tissues examined. In the abnormal organs of the NbDEK VIGS lines, protein levels of D-type cyclins (CycD)2, CycD3, and proliferating cell nuclear antigen (PCNA) were greatly elevated, and transcription of E2F (E2 promoter binding factor), E2F-regulated genes, retinoblastoma (Rb), and KNOTTED1 (KN1)-type homeobox genes was also stimulated. These results suggest that phytocalpain is a key regulator of cell proliferation and differentiation during plant organogenesis, and that it acts partly by controlling the CycD/Rb pathway.
Keyword
CycDE2F-regulated genesInhibited cell differentiationProlonged cell proliferationVirus-induced gene silencing
ISSN
0960-7412
Publisher
Wiley
DOI
http://dx.doi.org/10.1111/j.1365-313X.2004.02102.x
Type
Article
Appears in Collections:
Division of Biomaterials Research > Bionanotechnology Research Center > 1. Journal Articles
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