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Please use this identifier to cite or link to this item:
http://hdl.handle.net/10174/4228
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Title: | Cell cycle maneuvering: a strategy taken by plant parasitic nematode to induce specialized feeding sites in plant roots. |
Authors: | Paulo, Vieira Engler, G. Mota, Manuel Abad, Pierre de Veylder, L. Almeida Engler, J |
Keywords: | plant parasitic nematode feeding sites Meloidogyne |
Issue Date: | 16-Jul-2011 |
Citation: | Vieira, P., Engler, G., Mota, M., Abad, P., de Veylder, L. & de Almeida Engler, J. 2011. Cell cycle maneuvering: a strategy taken by plant parasitic nematode to induce specialized feeding sites in plant roots. Society of Nematologists 50th Anniversary Meeting. 16-21 July, Corvallis, Oregon, USA. |
Abstract: | Plant-parasitic nematodes of the genera Meloidogyne are capable to induce giant cells
that undergo repeated mitosis without cytokinesis possibly alternated with endoreduplication
cycles. Promoter activity and mRNA localization of key cell cycle genes like CDKA;1,
CDKB1;1, CYCB1;1, and CYCA2;1 showed early induction of these genes in both nematode
feeding site (NFS). In addition, disturbance in NFS development and nematode maturation
were observed during treatment of infected roots with cell cycle inhibitors. DNA synthesis
experiments demonstrated that both feeding sites undergo extra endocycles possibly justifying
the large nuclei present in NFC. How precisely nematodes manipulate the cell cycle in their
favor remains to be understood. A systematic comparison of the temporal and spatial
expression pattern of different classes of core cell cycle genes between uninfected roots and
nematode infected Arabidopsis thaliana plants resulted in the identification of a collection of
genes possibly implicated in NFC development. Among them, one member of the so-called
interactors of cyclin-dependent kinase/Kip-related proteins (ICK/KRP), negative regulators of
the cell cycle, showed to be upregulated during NFS development. Recent work has shown
that KRP2 might regulate mitosis-to-endocycle transition during Arabidopsis leaf
development and is highly expressed in endoreduplicating cells as potentially occurring in
nematode feeding cells KRPs. To address the direct relevance of these cell cycle inhibitors
genes for NFS ontogeny, mutant lines over- expressing and knocking-down are being used to
determine how NFS development is affected, and which family members are potential
involved in the NFS formation. Furthermore, in vivo subcellular localization of these cell
cycle proteins in NFS has been followed to understand the dynamics of these proteins during
giant cell development. Based on our preliminary results, some of these cell cycles inhibitors
genes are promising candidates involved in NFS development. |
URI: | http://hdl.handle.net/10174/4228 |
Type: | lecture |
Appears in Collections: | BIO - Comunicações - Em Congressos Científicos Internacionais
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