Octavio Martínez

Dr. Octavio Martínez

CINVESTAV–LANGEBIO, Irapuato, Guanajuato, 36500, México
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Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

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

Representative Publications

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1 April 2000 in Nature Biotechnology
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JLJosé López-Bucio
José López-Bucio
Octavio MartínezOctavio Martínez
Octavio Martínez
AGArturo Guevara-García
Arturo Guevara-García
Luis Herrera-EstrellaLuis Herrera-Estrella
Luis Herrera-Estrella

1 December 1992 in Theoretical and Applied Genetics
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Octavio MartínezOctavio Martínez
Octavio Martínez
RCR. N. Curnow
R. N. Curnow

14 December 2015 in Proceedings of the National Academy of Sciences
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LYLenin Yong-Villalobos
Lenin Yong-Villalobos
SGSandra Isabel González-Morales
Sandra Isabel González-Morales
KWKazimierz Wrobel
Kazimierz Wrobel
DGDolores Gutiérrez-Alanis
Dolores Gutiérrez-Alanis
SCSergio Alan Cervantes-Peréz
Sergio Alan Cervantes-Peréz
Luis Herrera-EstrellaLuis Herrera-Estrella
Luis Herrera-Estrella
Significance: Significant progress has been achieved in our understanding of plant adaptive responses to ensure growth and reproduction in soils with low phosphate (Pi) availability. However, the potential role of epigenetic mechanisms in the modulation of these responses remains largely unknown. In this article, we describe dynamic changes in global DNA methylation patterns that occur in Arabidopsis plants exposed to low Pi availability; these changes are associated with the onset of Pi starvation responses. We show that the expression of a subset of low Pi-responsive genes is modulated by methylation changes and that DNA methylation is required for the proper establishment of developmental and molecular responses to Pi starvation.

9 February 2012 in PLOS ONE
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Martin HeilMartin Heil
Martin Heil
EIEnrique Ibarra-Laclette
Enrique Ibarra-Laclette
RARosa M. Adame-Álvarez
Rosa M. Adame-Álvarez
Octavio MartínezOctavio Martínez
Octavio Martínez
EREnrique Ramirez-Chávez
Enrique Ramirez-Chávez
Luis Herrera-EstrellaLuis Herrera-Estrella
Luis Herrera-Estrella
Animal-derived elicitors can be used by plants to detect herbivory but they function only in specific insect–plant interactions. How can plants generally perceive damage caused by herbivores? Damaged-self recognition occurs when plants perceive molecular signals of damage: degraded plant molecules or molecules localized outside their original compartment. Flame wounding or applying leaf extract or solutions of sucrose or ATP to slightly wounded lima bean (Phaseolus lunatus) leaves induced the secretion of extrafloral nectar, an indirect defense mechanism. Chemically related molecules that would not be released in high concentrations from damaged plant cells (glucose, fructose, salt, and sorbitol) did not elicit a detectable response, excluding osmotic shock as an alternative explanation. Treatments inducing extrafloral nectar secretion also enhanced endogenous concentrations of the defense hormone jasmonic acid (JA). Endogenous JA was also induced by mechanically damaging leaves of lima bean, Arabidopsis, maize, strawberry, sesame and tomato. In lima bean, tomato and sesame, the application of leaf extract further increased endogenous JA content, indicating that damaged-self recognition is taxonomically widely distributed. Transcriptomic patterns obtained with untargeted 454 pyrosequencing of lima bean in response to flame wounding or the application of leaf extract or JA were highly similar to each other, but differed from the response to mere mechanical damage. We conclude that the amount or concentration of damaged-self signals can quantitatively determine the intensity of the wound response and that the full damaged-self response requires the disruption of many cells. Numerous compounds function as JA-inducing elicitors in different plant species. Most of them are, contain, or release, plant-derived molecular motifs. Damaged-self recognition represents a taxonomically widespread mechanism that contributes to the perception of herbivore feeding by plants. This strategy is independent of insect-derived elicitors and, therefore, allows plants to maintain evolutionary control over their interaction with herbivores.

15 July 2008 in Proceedings of the National Academy of Sciences
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Octavio MartínezOctavio Martínez
Octavio Martínez
MRM. Humberto Reyes-Valdés
M. Humberto Reyes-Valdés
The transcriptome is a set of genes transcribed in a given tissue under specific conditions and can be characterized by a list of genes with their corresponding frequencies of transcription. Transcriptome changes can be measured by counting gene tags from mRNA libraries or by measuring light signals in DNA microarrays. In any case, it is difficult to completely comprehend the global changes that occur in the transcriptome, given that thousands of gene expression measurements are involved. We propose an approach to define and estimate the diversity and specialization of transcriptomes and gene specificity. We define transcriptome diversity as the Shannon entropy of its frequency distribution. Gene specificity is defined as the mutual information between the tissues and the corresponding transcript, allowing detection of either housekeeping or highly specific genes and clarifying the meaning of these concepts in the literature. Tissue specialization is measured by average gene specificity. We introduce the formulae using a simple example and show their application in two datasets of gene expression in human tissues. Visualization of the positions of transcriptomes in a system of diversity and specialization coordinates makes it possible to understand at a glance their interrelations, summarizing in a powerful way which transcriptomes are richer in diversity of expressed genes, or which are relatively more specialized. The framework presented enlightens the relation among transcriptomes, allowing a better understanding of their changes through the development of the organism or in response to environmental stimuli.