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Functional Genomics
•Functional genomic datasets•Biological networks•Integrating genomic datasets
BIO520 Bioinformatics Jim Lund
Functional genomics
• Genome scale experiments to understand the function of all the proteins--what they do and how they interact.
• Many different experimental designs– Different kinds of information generated.
• Each has experimental limitations– Coverage: full genome, limited?– False positives.– False negatives.
Reporter Gene
BaitProtein
BindingDomain
Prey Protein
ActivationDomain
• Two hybrid proteins are generated with transcription factor domains
• Both fusions are expressed in a yeast cell that carries a reporter gene whose expression is under the control of binding sites for the DNA-binding domain
The Two-Hybrid Systemfor identifying protein/protein binding pairs
Reporter Gene
BaitProtein
BindingDomain
Prey Protein
ActivationDomain
The Two-Hybrid System
• Interaction of bait and prey proteins localizes the activation domain to the reporter gene, thus activating transcription.
• Since the reporter gene typically codes for a survival factor, yeast colonies will grow only when an interaction occurs.
Interactions shown as a network
Networks
• When methods of detecting functional linkages are applied to all the proteins of an organism, network of interacting, functionally linked proteins can be traced.
• As methods improve for detecting protein linkages, it seems likely that most of the proteins will be included in the network.
What do you miss?
• Tertiary interactions• Regulated interactions
– Subcellular localization dependent
– Cofactor dependent (eg. Hormone-regulated)
• Low-affinity (Kd>10-6)
• Immunolocalization– FUSION PROTEINS
• Prediction– Membrane vs non-membrane
• improved by homology
• WHICH MEMBRANE
– Nuclear vs cytoplasmic
Cellular Location
YFG GFP
Drosophila Fusion Project (FlyTrap)
• Exon GFP vector– Inserts fairly randomly.
• Fluorescent sort thousands of embryos.– Find embryos with an
insertion that produces GFP expression.
• Image– Capture and analyze
images• Curate by hand.• Computer image
analysis and classification.
Developmental Localization
Mouse genomic gene expression• Allen Brain Atlas (ABA) is an interactive, genome-wide
image database of gene expression in the mouse and human brain. 17,000 mouse gene expression patterns, cortex expression for 2,000 human genes.
Allen Brain Atlas
3D mouse gene expression project
Single gene expression database for the mouse research community. Integrated in the Mouse Genome Database (MGD) at the Jackson Laboratory.
10,302 expression entries
WT1 expression (red) on a section of the E9 (Theiler Stage 14) embryo from the Edinburgh Mouse Atlas. The gut epithelium is shown in yellow and the neural tube in a blue overlay. WT1 is expressed in the presumptive mesothelium of the coelom and in the intermediate mesoderm (ventral to the somites).
Methods for discovering protein function
•Automated Binding Assays•High Throughput Enzyme Assays
Genome-wide Knockouts
• Yeast Genome– Recombination
strategy
• Mouse Genome
• More in Functional Genomics!!!
Essential vs Non-essential
• Transcription similar– >99% essential genes transcribed
• Transcript level 70% higher
– >90% non-essential transcribed
• Genome locations similar– Not clustered
– Essential genes rarely near telomeres
Why only 20% essential?
• Redundant– 8.5% of non-essential had CLOSE
homolog in genome (P<10-150)• Essential in another condition• Marginal Benefit
Resources
YEAST• Saccharomyces
Genome Deletion Project– http://www-sequence.st
anford.edu/group/yeast_deletion_project/deletions3.html
MOUSE• Mouse Phenome Database
– http://phenome.jax.org/pub-cgi/phenome/mpdcgi?rtn=docs/home
• Knockout Mouse Project– http://www.knockoutmouse.org/
Genome-Scale Biochemical Assay
• Protein arrays-biochemically active
Databases
• Relationships between genes/proteins.
• How are different types of experimental data integrated?– Schema
• Data quality– Who curates?– Who revises?
Proteome Projects• SwissProt (ExPasy)
– http://expasy.org/ch2d/
• Saccharomyces Genome Database (SGD) Gene Function Information– 2-hybrid, functional assignments, pathways.– http://www.yeastgenome.org/SearchContents.shtml
• Yale TRIPLES– Database of TRansposon-Insertion
Phenotypes, Localization, and Expression in Saccharomyces.
• 2-hybrid databases– http://proteome.wayne.edu/YTHwebsites.html
Pathway and interaction databases
• KEGG (http://www.genome.jp/kegg/)
– Metabolic and signaling pathways• PUMA (http://compbio.mcs.anl.gov/puma2/cgi-bin/index.cgi)
– Metabolic and signaling pathways• DIP (http://dip.doe-mbi.ucla.edu/)
– Protein-protein interactions• BIND (http://bind.ca/)
– Molecular and genetic interactions
KEGG pathway map
Pentose phosphate cycle
Purine metabolism
HISTIDINE METABOLISM
2.4.2.17
3.6.1.31
3.5.4.19
5.3.1.16
2.4.2.-4.2.1.1
92.6.1.9
3.1.3.15
3.5.1.-
2.6.1.-Phosphoribulosyl-Formimino-AICAR-P
Phosphoribosyl-Formimino-AICAR-P
Phosphoribosyl-AMP
Phosphoriboxyl-ATPPRPP
5P-D-1-ribulosyl-formimine
Imidazole-Glicerol-3P
Imidazole-acetole P
L-Histidinol-P
1.1.1.23
2.1.1.-
6.3.2.11
2.1.1.22
6.3.2.11
3.4.13.5
3.4.13.20
3.4.13.3
4.1.1.22
4.1.1.28
1.4.3.61.2.1.31.1413
53.5.2.-3.5.3.5
N-Formyl-L-aspartate
Imidazoloneacetate
Imidazole-4-acetate
Imidazoleacetaldehyde Histamine
Carnosine
Aneserine
1.1.1.23
6.1.1
1-Methyl-L-histidine
L-Hisyidinal
L-Hisyidinal
5P Ribosyl-5-amino 4-Imidazole carboxamide(AICAR)
L-Histidine
Hercyn
Integrating pathway and expression dataThe list of genes being activated or inactivated or that are unaffected when comparing two samples becomes more informative if the genes can be mapped onto maps from which functions can be deduced.