Ana Campilho

Dr. Ana Campilho

1. CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, InBIO Laboratório Associado, Campus de Vairão, Universidade do Porto, 4485-661 Vairão, Portugal
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orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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21 April 2010 in Nature
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Journal Article
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ACAnnelie Carlsbecker
Annelie Carlsbecker
JLJi-Young Lee
Ji-Young Lee
CRChristina J. Roberts
Christina J. Roberts
JDJan Dettmer
Jan Dettmer
SLSatu Lehesranta
Satu Lehesranta
PBPhilip N. Benfey
Philip N. Benfey

1 December 2011 in Developmental Cell
Verified
Journal Article
Closed access
AVAnne Vatén
Anne Vatén
JDJan Dettmer
Jan Dettmer
SWShuang Wu
Shuang Wu
YSYork-Dieter Stierhof
York-Dieter Stierhof
SMShunsuke Miyashima
Shunsuke Miyashima
YHYkä Helariutta
Ykä Helariutta

15 May 2017 in New Phytologist
Verified
Journal Article
Open access
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KRKamil Růžička
Kamil Růžička
MZMi Zhang
Mi Zhang
ACAna Campilho
Ana Campilho
ZBZsuzsanna Bodi
Zsuzsanna Bodi
MKMuhammad Kashif
Muhammad Kashif
RFRupert Fray
Rupert Fray
Summary: N6‐adenosine methylation (m6A) of mRNA is an essential process in most eukaryotes, but its role and the status of factors accompanying this modification are still poorly understood. Using combined methods of genetics, proteomics and RNA biochemistry, we identified a core set of mRNA m6A writer proteins in Arabidopsis thaliana. The components required for m6A in Arabidopsis included MTA, MTB, FIP37, VIRILIZER and the E3 ubiquitin ligase HAKAI. Downregulation of these proteins led to reduced relative m6A levels and shared pleiotropic phenotypes, which included aberrant vascular formation in the root, indicating that correct m6A methylation plays a role in developmental decisions during pattern formation. The conservation of these proteins amongst eukaryotes and the demonstration of a role in writing m6A for the E3 ubiquitin ligase HAKAI is likely to be of considerable relevance beyond the plant sciences.

1 December 2005 in Cell
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Journal Article
Closed access
MWMarjolein Wildwater
Marjolein Wildwater
ACAna Campilho
Ana Campilho
Jose Manuel Perez-PerezJose Manuel Perez-Perez
Jose Manuel Perez-Perez
RHRenze Heidstra
Renze Heidstra
IBIkram Blilou
Ikram Blilou
BSBen Scheres
Ben Scheres

1 December 2008 in Developmental Cell
Verified
Journal Article
Closed access
VWViola Willemsen
Viola Willemsen
MBMarion Bauch
Marion Bauch
TBTom Bennett
Tom Bennett
ACAna Campilho
Ana Campilho
HWHarald Wolkenfelt
Harald Wolkenfelt
BSBen Scheres
Ben Scheres

1 March 2010 in The Plant Cell
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Journal Article
Closed access
TBTom Bennett
Tom Bennett
ATAlbert van Den Toorn
Albert van Den Toorn
GSGabino F. Sanchez-Perez
Gabino F. Sanchez-Perez
ACAna Campilho
Ana Campilho
VWViola Willemsen
Viola Willemsen
BSBen Scheres
Ben Scheres
The root cap has a central role in root growth, determining the growth trajectory and facilitating penetration into the soil. Root cap cells have specialized functions and morphologies, and border cells are released into the rhizosphere by specific cell wall modifications. Here, we demonstrate that the cellular maturation of root cap is redundantly regulated by three genes, SOMBRERO (SMB), BEARSKIN1 (BRN1), and BRN2, which are members of the Class IIB NAC transcription factor family, together with the VASCULAR NAC DOMAIN (VND) and NAC SECONDARY WALL THICKENING PROMOTING FACTOR (NST) genes that regulate secondary cell wall synthesis in specialized cell types. Lateral cap cells in smb-3 mutants continue to divide and fail to detach from the root, phenotypes that are independent of FEZ upregulation in smb-3. In brn1-1 brn2-1 double mutants, columella cells fail to detach, while in triple mutants, cells fail to mature in all parts of the cap. This complex genetic redundancy involves differences in expression, protein activity, and target specificity. All three genes have very similar overexpression phenotypes to the VND/NST genes, indicating that members of this family are largely functionally equivalent. Our results suggest that Class IIB NAC proteins regulate cell maturation in cells that undergo terminal differentiation with strong cell wall modifications.