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Edinburgh, Scotland, United Kingdom - TAIR

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Sequencing across the genome-phenome<br />

divide<br />

The development of DNA sequencing technologies producing vast amounts of<br />

sequence information has triggered a paradigm shift in biology, enabling<br />

massively parallel surveying of complex nucleic acid populations. The diversity<br />

of applications to which these technologies have already been applied<br />

demonstrates the immense range of cellular processes and properties that can<br />

now be studied at the single-base resolution. As part of the Arabidopsis 1001<br />

genomes project (http://1001genome.org project), we have carried out both<br />

resequencing and de novo sequencing and assembly of several accessions. In<br />

parallel, we developed RNA-Seq and MethylC-Seq methods which now allow<br />

sequence-level maps of the transcriptome and cytosine DNA methylome,<br />

respectively. When combined with the genome sequences, an in depth view of<br />

the relationship between genetic and epigenetic variation and their effects on<br />

gene expression can be obtained. In addition, we have applied now-generation<br />

DNA sequencing approaches to identify the sites of insertion of T-DNA in large<br />

populations of arrayed plants. This approach should enable completion of the<br />

Arabidopsis Unimutant Project, which aims to identify sequence-indexed<br />

homozygous insertion mutations for all genes in the Col-0 genome (see<br />

http://signal.salk.edu). Finally, a major deficiency in the repertoire of plant<br />

genomic resources is the paucity of large-scale protein-protein and protein-DNA<br />

information for Arabidopsis or any plant system. Genome-wide molecular<br />

interaction maps (interactomes) are an indispensible tool for systems biology,<br />

aid focused biological studies, provide network information for topological<br />

analysis and aid the development of large-scale dynamic models. We have<br />

created a first generation plant interactome map in a collaboration led by the<br />

Center for Cancer Systems Biology. Utilizing both high throughput, high-quality<br />

yeast-2-hybrid and improved protein array technologies, a 9k by 9k binary<br />

interaction map has been developed using a recombination-vector based<br />

ORFeome collection of sequence-validated Arabidopsis open reading frame<br />

(ORF) clones. Properties of this first generation plant protein-protein interactome<br />

map, examples of its utility and examples of novel biological insights derived<br />

from it will be described.<br />

63<br />

C12<br />

Wednesday 16:00 - 16:30<br />

Tools and Resources<br />

Joseph Ecker<br />

The Salk Institute<br />

La Jolla<br />

CA<br />

USA

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