I am a Postdoctoral fellow in [[Maloof_Lab |Julin Maloof's lab]] in the [http://www-plb.ucdavis.edu/ Section of Plant Biology] at the [http://www.ucdavis.edu University of California Davis].<br>
I am a Postdoctoral fellow in [[Maloof_Lab |Julin Maloof's lab]] in the [http://www-plb.ucdavis.edu/ Section of Plant Biology] at the [http://www.ucdavis.edu University of California Davis].<br>
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In 2005, I completed my PhD. in JM Martinez-Zapater's lab at the [http://www.cnb.uam.es CNB] (National Center for Biotechnology) in Madrid, Spain, where I performed a quantitative genetic analysis of flowering time in tomato <cite>Jimenez-Gomez07</cite>.
In 2005, I completed my PhD. in JM Martinez-Zapater's lab at the [http://www.cnb.uam.es CNB] (National Center for Biotechnology) in Madrid, Spain, where I performed a quantitative genetic analysis of flowering time in tomato <cite>Jimenez-Gomez07</cite>.<br>
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My main interests are based on the application of modern genetic and bioinformatic techniques to the study of plant evolution. To do this I survey different species and natural populations of plants presenting variation in interesting characteristics, and analyze the responsible molecular mechanism. Here is an small description of some of my work:
My main interests are based on the application of modern genetic and bioinformatic techniques to the study of plant evolution. To do this I survey different species and natural populations of plants presenting variation in interesting characteristics, and analyze the responsible molecular mechanism. Here is an small description of some of my work:
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We use a bioinformatic approach to scrutinize the available tomato EST sequences and detect Single Nucleotide Polymorphisms. This will allow us to estimate the divergence between wild and cultivated tomato species, and will serve to have an idea of the effectiveness of the high throughput genomic methods that are and will be available soon for these species.
We use bioinformatics to detect Single Nucleotide Polymorphisms among tomato EST sequences available in the databases. This will allow us to estimate divergence rates over large regions of the genome of selected species, and will render a new set of molecular markers useful in natural variation studies. In addition we will determine the possibilities that the newly available high throughput genomic methods have on these species.
In 2005, I completed my PhD. in JM Martinez-Zapater's lab at the CNB (National Center for Biotechnology) in Madrid, Spain, where I performed a quantitative genetic analysis of flowering time in tomato [1].
My main interests are based on the application of modern genetic and bioinformatic techniques to the study of plant evolution. To do this I survey different species and natural populations of plants presenting variation in interesting characteristics, and analyze the responsible molecular mechanism. Here is an small description of some of my work:
QTL analysis of the shade avoidance response in Arabidopsis
It is well known that plants from different light environments exhibit different degrees of responsiveness to similar light stimulus. Plants accommodated to sunny environments detect foliar shade from neighboring vegetation they respond increasing petiole and stem elongation and reducing the time to reproduction, a phenomenon called the "shade avoidance response". On the other hand, plants surrounded by tall vegetation are familiarized with the shade and do not present this response.
To identify the molecular mechanisms underlying this differences we are performing QTL analysis using a previously developed, well characterized Recombinant Inbred Line set descent from two different natural populations of Arabidopsis thaliana: Bayreuth, originary from the German low altitude fallow lands, and Shahdara, from the high mountains of Tadjikistan [2].
We grew replicated individual RILs in environments simulating shade and sun conditions and measured them for a number of traits characteristic of the shade avoidance response syndrome. For the QTL analysis we modeled this phenotipic data to calculate a shade avoidance response index and used an available genetic map that includes more than 500 Single Feature Polymorphism (SFP) markers [3].
LOD score graph for several of the traits measured
We are focusing now in a chromosomal region containing about 200 genes to fine map and identify the gene responsible for the differential response to shade between the two natural populations. To do this we employ traditional genetic approaches as well as genomic and network analysis. We are developing a protocol to construct gene networks that will help us consider candidate genes based on coexpression with other genes across microarray experiments [4], colocalization with expression QTLs [5], functional categorization [6] and presence of polymorphisms [7].
Fragment of a gene network
Single Nuncleotide Polymorphism discovery between wild Tomato species
We use bioinformatics to detect Single Nucleotide Polymorphisms among tomato EST sequences available in the databases. This will allow us to estimate divergence rates over large regions of the genome of selected species, and will render a new set of molecular markers useful in natural variation studies. In addition we will determine the possibilities that the newly available high throughput genomic methods have on these species.
Molecular evolution of PHYTOCHROME B
PHYTOCHROME B (PHYB) is the main plant photoreceptor involved in the shade avoidance response. This gene has been reported to be under selective pressure, suggesting that plants with different shade avoidance responses may have different functional alleles of PHYB. Under these presumptions we are sequencing and cloning PHYB genes from a number of species with diverse shade avoidance behaviors. We will soon test if the variation in light responses between these plants are due to particular amino-acid changes in this photoreceptor.
amino-acid changes in a fragment of the PHYB gene in 8 speceis, red and black bars indicate non conserverd/ conserved amino-acid changes respectively
Proteomics of light perception
When plants are exposed to light a number of changes occur that are controlled by complex signaling processes. Light perception includes interaction with flowering time pathways, the circadian clock and hormone pathways between others. Genetics and genomic analysis have so far allowed us to identify and understand part of how this signals occur at the gene expression level, but very little is known about the changes produced in the plant at protein level. The new advances in Proteomics make possible to identify small protein changes with high precision. In collaboration with the Proteomics Facility at the UC Davis Genome Center we are preparing a set of experiments that will allow us to determine the accuracy and power of the newest techniques in protein quantification and to better understand how the proteome is regulated by light.
