Robert Doczi

Dr. Robert Doczi

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Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2004 in Molecular Cell
Verified
Journal Article
Closed access
Markus TeigeMarkus Teige
Markus Teige
ESElisabeth Scheikl
Elisabeth Scheikl
TEThomas Eulgem
Thomas Eulgem
RDRobert Doczi
Robert Doczi
KIKazuya Ichimura
Kazuya Ichimura
HHHeribert Hirt
Heribert Hirt

1 July 2007 in The Plant Cell
Verified
Journal Article
Closed access
ASAlois Schweighofer
Alois Schweighofer
VKVaiva Kazanaviciute
Vaiva Kazanaviciute
ESElisabeth Scheikl
Elisabeth Scheikl
Markus TeigeMarkus Teige
Markus Teige
RDRobert Doczi
Robert Doczi
IMIrute Meskiene
Irute Meskiene
Wound signaling pathways in plants are mediated by mitogen-activated protein kinases (MAPKs) and stress hormones, such as ethylene and jasmonates. In Arabidopsis thaliana, the transmission of wound signals by MAPKs has been the subject of detailed investigations; however, the involvement of specific phosphatases in wound signaling is not known. Here, we show that AP2C1, an Arabidopsis Ser/Thr phosphatase of type 2C, is a novel stress signal regulator that inactivates the stress-responsive MAPKs MPK4 and MPK6. Mutant ap2c1 plants produce significantly higher amounts of jasmonate upon wounding and are more resistant to phytophagous mites (Tetranychus urticae). Plants with increased AP2C1 levels display lower wound activation of MAPKs, reduced ethylene production, and compromised innate immunity against the necrotrophic pathogen Botrytis cinerea. Our results demonstrate a key role for the AP2C1 phosphatase in regulating stress hormone levels, defense responses, and MAPK activities in Arabidopsis and provide evidence that the activity of AP2C1 might control the plant's response to B. cinerea.

12 October 2007 in The Plant Cell
Verified
Journal Article
Closed access
RDRobert Doczi
Robert Doczi
GBGünter Brader
Günter Brader
APAladár Pettkó-Szandtner
Aladár Pettkó-Szandtner
IRIva Rajh
Iva Rajh
ADArmin Djamei
Armin Djamei
Heribert HirtHeribert Hirt
Heribert Hirt
Although the Arabidopsis thaliana genome contains genes encoding 20 mitogen-activated protein kinases (MAPKs) and 10 MAPK kinases (MAPKKs), most of them are still functionally uncharacterized. In this work, we analyzed the function of the group B MAPK kinase, MKK3. Transgenic ProMKK3:GUS lines showed basal expression in vascular tissues that was strongly induced by Pseudomonas syringae pv tomato strain DC3000 (Pst DC3000) infection but not by abiotic stresses. The growth of virulent Pst DC3000 was increased in mkk3 knockout plants and decreased in MKK3-overexpressing plants. Moreover, MKK3 overexpression lines showed increased expression of several PR genes. By yeast two-hybrid analysis, coimmunoprecipitation, and protein kinase assays, MKK3 was revealed to be an upstream activator of the group C MAPKs MPK1, MPK2, MPK7, and MPK14. Flagellin-derived flg22 peptide strongly activated MPK6 but resulted in poor activation of MPK7. By contrast, MPK6 and MPK7 were both activated by H(2)O(2), but only MPK7 activation was enhanced by MKK3. In agreement with the notion that MKK3 regulates the expression of PR genes, ProPR1:GUS expression was strongly enhanced by coexpression of MKK3-MPK7. Our results reveal that the MKK3 pathway plays a role in pathogen defense and further underscore the importance and complexity of MAPK signaling in plant stress responses.

1 September 2012 in Trends in Plant Science
Verified
Journal Article
Closed access
RDRobert Doczi
Robert Doczi
LÖLászló Ökrész
László Ökrész
ARAlfonso E. Romero
Alfonso E. Romero
APAlberto Paccanaro
Alberto Paccanaro
LBLászló Bögre
László Bögre

15 July 2008 in New Phytologist
Verified
Journal Article
Open access
PDF file
MMMargit Menges
Margit Menges
RDRobert Doczi
Robert Doczi
LÖLászló Ökrész
László Ökrész
PMPiero Angelo Morandini
Piero Angelo Morandini
LMLuca Mizzi
Luca Mizzi
LBLászló Bögre
László Bögre
• Mitogen activated protein kinase (MAPK) pathways are signal transduction modules with layers of protein kinases having c. 120 genes in Arabidopsis, but only a few have been linked experimentally to functions. • We analysed microarray expression data for 114 MAPK signalling genes represented on the ATH1 Affymetrix arrays; determined their expression patterns during development, and in a wide range of time-course microarray experiments for their signal-dependent transcriptional regulation and their coregulation with other signalling components and transcription factors. • Global expression correlation of the MAPK genes with each of the represented 21 692 Arabidopsis genes was determined by calculating Pearson correlation coefficients. To group MAPK signalling genes based on similarities in global regulation, we performed hierarchical clustering on the pairwise correlation values. This should allow inferring functional information from well-studied MAPK components to functionally uncharacterized ones. Statistical overrepresentation of specific gene ontology (GO) categories in the gene lists showing high expression correlation values with each of the MAPK components predicted biological themes for the gene functions. • The combination of these methods provides functional information for many uncharacterized MAPK genes, and a framework for complementary future experimental dissection of the function of this complex family.

25 December 2017 in FEBS Letters
Verified
Journal Article
Open access
PDF file
MDMagdalena Dory
Magdalena Dory
EHElizabeth Hatzimasoura
Elizabeth Hatzimasoura
BKBrigitta M. Kállai
Brigitta M. Kállai
SNSzilvia K. Nagy
Szilvia K. Nagy
KJKatalin Jäger
Katalin Jäger
RDRobert Doczi
Robert Doczi
Plant growth flexibly adapts to environmental conditions, implying cross‐talk between environmental signalling and developmental regulation. Here, we show that the PIN auxin efflux carrier family possesses three highly conserved putative mitogen‐activated protein kinase (MAPK) sites adjacent to the phosphorylation sites of the well‐characterised AGC kinase PINOID, which regulates the polar localisation of PINs and directional auxin transport, thereby underpinning organ growth. The conserved sites of PIN1 are phosphorylated in vitro by two environmentally activated MAPKs, MPK4 and MPK6. In contrast to AGC kinases, MAPK‐mediated phosphorylation of PIN1 at adjacent sites leads to a partial loss of the plasma membrane localisation of PIN1. MAPK‐mediated modulation of PIN trafficking may participate in environmental adjustment of plant growth.