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Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

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Record number 541280
Title Ditr P79_Characterisation of PLETHORA during gall formation of the root-knot nematode Meloidogyne incognita
Author(s) Oosterbeek, Matthijs; Overmars, H.A.; Scheres, B.J.G.; Bakker, J.; Goverse, A.
Event ESN Conference 2018, Ghent, 2018-09-09/2018-09-13
Department(s) Laboratory of Nematology
EPS
Laboratory of Molecular Biology
PE&RC
Publication type Poster (scientific)
Publication year 2018
Abstract The parasitic root-knot nematode Meloidogyne incognita manipulates developmental processes in plants through formation of large tumour-like structures, designated as galls, in the roots of their hosts. The transcriptional profile of these galls show significant overlap with that of the formation of lateral roots (Cabrera et al., 2014). Key regulators in the formation of lateral roots are the PLETHORA (PLT) transcription factors PLT3, PLT5 and PLT7. They are induced by the sustained presence of the phytohormone auxin. These genes work together to regulate positioning and outgrowth of lateral root primordia (Hofhuis et al., 2013). The auxin efflux proteins PINFORMED (PIN) are thought to play an important role in this process and PLTs are known to regulate them in plants (Prasad et al., 2011). During the initial development of nematode-induced galls an accumulation of auxin is observed (Karczmarek et al., 2004). Additionally PIN proteins are known to be involved in gall formation (Kyndt et al., 2016). However, how the PIN proteins are regulated upon root-knot nematode infection is unknown. Hence, we studied the possibility that the PLT-PIN module is used during the formation of feeding sites of M. incognita. Mutant lines of the PLT genes showed a decrease in the number of infections and in number of reproducing females as compared to the wild type lines. Additionally, in several mutant lines galls developed that were significantly increased in size. Moreover, the auxin exporter PIN3 in the mutant line of the three PLT genes was no longer localised at the plasma membranes of cells within the feeding site in contrast to the wild type lines. We conclude that the three PLT genes are involved in feeding site initiation and development and could potentially achieve this through regulation of PIN.
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