idea: measure the amount of mrna to see which genes are being expressed in (used by) the cell....

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Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently harder. Measuring Gene Expression

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Page 1: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently harder.

Measuring Gene Expression

Page 2: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Central Assumption of Gene Expression Microarrays

• The level of a given mRNA is positively correlated with the expression of the associated protein.– Higher mRNA levels mean higher protein

expression, lower mRNA means lower protein expression

• Other factors:– Protein degradation, mRNA degradation,

polyadenylation, codon preference, translation rates, alternative splicing, translation lag…

Page 3: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Principal Uses of Microarrays

• Genome-scale gene expression analysis– Differential gene expression between two (or

more) sample types– Responses to environmental factors– Disease processes (e.g. cancer)– Effects of drugs– Identification of genes associated with clinical

outcomes (e.g. survival)

Page 4: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Biological questionDifferentially expressed genesSample class prediction etc.

Testing

Biological verification and interpretation

Microarray experiment

Estimation

Experimental design

Image analysis

Normalization

Clustering Discrimination

Page 5: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Microarray example: Biomarker identification - lung cancer

SamplesSamples

Gen

eG

en

ess

Garber, Troyanskaya et al. Diversity of gene expression in adenocarcinoma of the lung. PNAS 2001, 98(24):13784-9.

Page 6: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

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Time (months)

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Cum. Survival (Group 3)

Cum. Survival (Group 2)

Cum. Survival (Group 1)

p = 0.002for Gr. 1 vs.

Gr. 3

Data partitioning clinically important: Patient survival for lung cancer subgroups

Garber, Troyanskaya et al. Diversity of gene expression in adenocarcinoma of the lung. PNAS 2001, 98(24):13784-9.

Page 7: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Technology basics• Microarrays are composed of short, specific DNA

sequences attached to a glass or silicon slide at high density

• A microarray works by exploiting the ability of an mRNA molecule to bind specifically to, or hybridize, the DNA template from which it originated

• RNA or DNA from the sample of interest is fluorescently-labeled so that relative or absolute abundances can be quantitatively measured

Page 8: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Two color vs single color

Bakel and Holstege. 2007. http://www.cell-press.com/misc/page?page=ETBR

Page 9: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Other applications of microarray technology

(besides measuring gene expression)

• DNA copy number analysis• SNP analysis• chIP-chip (interaction data)

• Competitive growth assays• …

Page 10: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Major technologies

• cDNA probes (> 200 nt), usually produced by PCR, attached to either nylon or glass supports

• Oligonucleotides (25-80 nt) attached to glass support

• Oligonucleotides (25-30 nt) synthesized in situ on silica wafers (Affymetrix)

• Probes attached to tagged beads

Page 11: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently
Page 12: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

cDNA Microarray Design

• Probe selection

– Non-redundant set of probes

– Includes genes of interest to project

– Corresponds to physically available clones

• Chip layout

– Grouping of probes by function

– Correspondence between wells in microtiter plates and spots on the chip

Page 13: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Building the chip

Ngai Lab arrayer , UC Berkeley

Print-tip head

Page 14: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

http://transcriptome.ens.fr/sgdb/presentation/principle.php

Page 15: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Example dual channel cDNA array results

Page 16: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently
Page 17: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Affymetrix GeneChips

• Probes are oligos synthesized in situ using a photolithographic approach

• Typically there are multiple oligos per cDNA, plus an equal number of negative controls

• The apparatus requires a fluidics station for hybridization and a special scanner

• Only a single fluorochrome is used per hybridization

Page 18: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

There may be 5,000-100,000 probe sets per chipA probe set = 11-20 PM, MM pairs

Affy

Page 19: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

http://www.weizmann.ac.il/home/ligivol/pictures/system.jpg

Page 20: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently

Interpreting Affymetrix OutputPerfect Match/Mismatch Strategy

• Each probe designed to be perfectly complementary to a target sequence, a partner probe is generated that is identical except for a single base mismatch in its center.

• These probe pairs, called the Perfect Match probe (PM) and the Mismatch probe (MM), allow the quantitation and subtraction of signals caused by non-specific cross-hybridization.

• The difference in hybridization signals between the partners serve as indicators of specific target abundance

Page 21: Idea: measure the amount of mRNA to see which genes are being expressed in (used by) the cell. Measuring protein might be more direct, but is currently