Projects
- Cereal Genome Mapping
- Cereal Plant Phenomics
- Enabling High-Resolution Mapping of in vivo Protein-DNA Interactions
- Making Fuel-Producing Microbes
Cereal Genome Mapping
Sequencing
of crop genomes provides deep insights into plant evolution and new tools
for crop improvement. The sequencing of giant and repetitive genomes such as
wheat and barley can be a challenge which requires worldwide collaborative
efforts.
A preliminary step to genome sequencing is the physical mapping, the construction of a scaffold of DNA segments where genes are positioned. Our project is working towards development of a physical map and ultimately a full genome sequence for barley chromosome 7H and wheat chromosomes 7A, 7B and 7D. These chromosomes carry loci controlling important traits including yield, quality, disease resistance and abiotic-stress tolerance. We evaluate the physical distance between markers along these chromosomes, assess their gene content and analyse how the genes recombine between parental lines for breeding of new varieties. Ultimately new genes will be discovered in wheat by shotgun sequencing of isolated chromosome arms using next-generation sequencing technologies.
We also aim to develop computational models describing relationships between genomes of wheat, barley and other cereals. This would enable the use of simpler genomes such as barley to accelerate assembly of the maps in corresponding regions of the more complex wheat genome.
PBRC researchers
- Ute Baumann
- Delphine Fleury
- Peter Langridge
- Bao Lam Huynh
- Andreas Schreiber
Collaborators
- Jaroslav Dolezel, Institute of Experimental Botany
- David Edwards, Australian Centre for Plant Functional Genomics
- Matthew Hayden, DPI Victorian AgriBiosciences Center
- Nils Stein, Leibniz Institute of Plant Genetics and Crop Plant Research
Cereal Plant Phenomics
The Australian Plant Phenomics Facility (APPF) provides state-of-the-art capabilities for plant phenotyping, offering controlled environments, field-based plant growth monitoring using high throughput robotics, and automated imaging and computing technologies that will generate up to 50 TB of data per year.
We will develop phenotyping software suitable for two vital food crops: wheat and barley. Datasets will be generated for diverse sets of germplasm covering collections of wild, landrace and cultivated lines in addition to genetic populations, mutant populations, and transgenic lines where particular genes have been silenced or over-expressed. For many of the lines, notably the genetic populations, additional datasets will also be available. These will include data from field trials covering yield and components of yield under a wide range of environmental conditions, maturity, and many other characteristics. In addition to these phenomic datasets, we will obtain transcriptomic and metabolomic datasets.
From the combined datasets, the ultimate objective is to develop models of the plant's response to environmental and developmental stimuli that can be traced back to specific biochemical or molecular events.
PBRC researchers
- Mahmood Golzarian
- Desmond Lun
- Mark Tester
Collaborators
- Bettina Berger, Australian Centre for Plant Functional Genomics
- James Eddes, Australian Centre for Plant Functional Genomics
- Karthika Rajendran, Australian Centre for Plant Functional Genomics
Enabling High-Resolution Mapping of in vivo Protein-DNA Interactions
Next-generation
sequencing technologies are revolutionizing biology and medicine by allowing
us to probe genetic structure and function and its effect on disease states
at a hitherto unknown level. In particular, next-generation sequencing
technologies permit ChIP-seq—an assay for observing in vivo
protein-DNA interactions, which are vital for cellular functions and are
involved in the mechanisms for many diseases, including cancer, genetic
diseases, and infectious diseases. Thus, ChIP-seq is an important
technology that is likely to have a profound impact on human health and,
with the falling cost of sequencing, it is a technology that is likely to
become more and more accessible. There is, however, a barrier to the
accessibility of ChIP-seq: bioinformatics tools for analysis of ChIP-seq
data are not yet at a stage that would allow them to be widely and easily
used by biologists and clinicians for fast, easy, and high-quality analysis.
We aim to develop robust and efficient computational and statistical methods that allow accurate and reliable identification of genomic loci associated with protein-DNA interaction from ChIP-seq data, leading ultimately to a user-friendly computational tool for ChIP-seq analysis that will be distributed for free for non-profit use through the World Wide Web, enabling fast, easy, and high-quality analysis for biologists and clinicians.
PBRC researchers
Collaborators
- Mark Borowsky, Massachusetts General Hospital
- James Galagan, Boston University
- Muriel Médard, Massachusetts Institute of Technology
- Brian Weiner, Broad Institute of MIT and Harvard
Making Fuel-Producing Microbes
The production of cheap, clean, renewable energy is one of the world's most
pressing problems. And microbes are a potential solution.
Microbes, such as blue-green algae, are capable of taking solar energy and storing it as a chemical fuel, thus allowing us to make use of the solar energy that continually bathes our planet in 10,000-fold abundance to our consumption. In contrast to the traditional solution of photovoltaic cells, solar microbial biofuel does not require expensive batteries for energy storage and, since microbes self-replicate, the capturing apparatus itself is potentially cheaper. Unfortunately, naturally-occurring microbes are not optimised for biofuel production from solar energy and must be engineered for this purpose.
We aim to engineer microbes that are useful for biofuel production using an approach that is grounded in mathematical modelling and computational design. We aim to engineer, in particular, a blue-green algae that converts solar energy and carbon dioxide into petroleum. Our activities include using and developing flux-balance metabolic models and their extensions, developing efficient algorithms for computational design and optimisation, and constructing engineered strains.
PBRC Researchers
Collaborators
- George Church, Harvard Medical School
- Caroline Colijn, University of Bristol
- Nicholas Guido, Harvard Medical School
- Graham Rockwell, Harvard Medical School
