Leandro Exequiel Lucero

Dr. Leandro Exequiel Lucero

Instituto de Agrobiotecnología del Litoral, Universidad Nacional del Litoral, CONICET, FHUC, Centro Científico Tecnológico CONICET Santa Fe, Colectora Ruta Nacional No 168 km. 0, Paraje El Pozo, Santa Fe 3000, Argentina
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Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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1 March 2020 in Molecular Cell
Verified
Journal Article
Closed access
FAFederico Ariel
Federico Ariel
LLLeandro Exequiel Lucero
Leandro Exequiel Lucero
ACAurelie Christ
Aurelie Christ
MMMaria Florencia Mammarella
Maria Florencia Mammarella
TJTeddy Jegu
Teddy Jegu
MCMartin Crespi
Martin Crespi

8 October 2015 in The Plant Journal
Verified
Journal Article
Closed access
PDF file
LLLeandro Exequiel Lucero
Leandro Exequiel Lucero
NUNora G. Uberti‐Manassero
Nora G. Uberti‐Manassero
AAAgustin Arce
Agustin Arce
FCFrancisco Colombatti
Francisco Colombatti
SASergio G. Alemano
Sergio G. Alemano
DGDaniel Gonzalez
Daniel Gonzalez

20 October 2011 in Journal of Experimental Botany
Verified
Journal Article
Open access
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NUNora G. Uberti-Manassero
Nora G. Uberti-Manassero
LLLeandro Exequiel Lucero
Leandro Exequiel Lucero
IVIvana Viola
Ivana Viola
AVAbelardo C. Vegetti
Abelardo C. Vegetti
DGDaniel Gonzalez
Daniel Gonzalez
The function of the class I TCP transcription factor TCP15 from Arabidopsis thaliana has been studied through the analysis of plants that express a fusion of this protein to the EAR repressor domain. Constitutive expression of TCP15-EAR produces growth arrest at the seedling stage, before leaf emergence. Expression of the repressor fusion from the AtTCP15 promoter produces small plants with leaves whose margins progressively curve upwards, starting from the basal part of the lamina. Leaves contain smaller and less differentiated cells, both on the adaxial and abaxial sides. The abaxial domain is relatively enlarged, with disorganized cells separated by empty spaces. TCP15-EAR also affects the growth of leaf petioles, flower pedicels, and anther filaments. Flowers show reduced elongation of the three outer whorls and altered gynoecia with irregular carpel surfaces and enlarged repla. Ectopic stigma-like structures develop from medial and basal parts of the replum. TCP15-EAR produces an increase in expression of the boundary-specific genes LOB, CUC1, and CUC2. Changes in CUC1 and CUC2 expression can be explained by the existence of lower levels of miR164 in leaves and the repression of IAA3/SHY2 and the SAUR-like gene At1g29460 in leaves and flowers. TCP15 binds to the promoter regions of IAA3/SHY2 and At1g29460, suggesting that these genes may be direct targets of the transcription factor. The results indicate that TCP15 regulates the expression of boundary-specific genes through a pathway that affects auxin homeostasis and partially overlaps with the one modulated by class II CIN-like TCP proteins.

14 April 2020 in EMBO Reports
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Journal Article
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RRRichard Rigo
Richard Rigo
JBJérémie Bazin
Jérémie Bazin
NRNatali Romero‐Barrios
Natali Romero‐Barrios
MMMichaël Moison
Michaël Moison
LLLeandro Exequiel Lucero
Leandro Exequiel Lucero
FAFederico Ariel
Federico Ariel

1 December 2017 in Molecular Plant
Verified
Journal Article
Closed access
LLLeandro Exequiel Lucero
Leandro Exequiel Lucero
PMPablo A. Manavella
Pablo A. Manavella
DGDiana E. Gras
Diana E. Gras
FAFederico Ariel
Federico Ariel
DGDaniel Gonzalez
Daniel Gonzalez

2 September 2020 in New Phytologist
Verified
Journal Article
Open access
PDF file
LLLeandro Exequiel Lucero
Leandro Exequiel Lucero
LFLucía Ferrero
Lucía Ferrero
CFCamille Fonouni‐Farde
Camille Fonouni‐Farde
FAFederico Ariel
Federico Ariel
Summary: The extraordinary maturation in high‐throughput sequencing technologies has revealed the existence of a complex network of transcripts in eukaryotic organisms, including thousands of long noncoding (lnc) RNAs with little or no protein‐coding capacity. Subsequent discoveries have shown that lncRNAs participate in a wide range of molecular processes, controlling gene expression and protein activity though direct interactions with proteins, DNA or other RNA molecules. Although significant advances have been achieved in the understanding of lncRNA biology in the animal kingdom, the functional characterization of plant lncRNAs is still in its infancy and remains a major challenge. In this review, we report emerging functional and mechanistic paradigms of plant lncRNAs and partner molecules, and discuss how cutting‐edge technologies may help to identify and classify yet uncharacterized transcripts into functional groups.