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Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100
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Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Dec 22, 2015

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Page 1: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Office hoursWednesday 3-4pm304A Stanley Hall

Review session5pm Thursday, Dec. 11

GPB100

Page 2: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Association vs. linkage

Strong, easy to detect, but rare in population;may not be reflective of common disease.Also, hard to collect family data.

Common but weak effects; need 1000’s of samples to detect.If no common cause, can fail.

Unrelatedindividuals

Relatedindividuals

Page 3: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Association vs. linkagesmall number of generations; individuals share big chunks of genome; can get co-inheritance between distant markers

many recombinations have happened since common ancestor;shared region is small; no co-inheritance between distant markers

So you need very high density of markers to get signal in an association study, but you get very high spatial resolution.

Page 4: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Association and admixture

Cases

Controls

=

=

At any one of these loci, Caucasian-like allele will be enriched in control samples.

Page 5: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Genotyping by array

Fig. 11.8

Page 6: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Expression microarrays

Fig. 1.13

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Labeled DNA sample vs. labeled mRNA (cDNA) sample

Page 8: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Labeled DNA sample vs. labeled mRNA (cDNA) sample

(reverse transcription in the test tube)

Page 9: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Coding sequence array

Fig. 1.13

Page 10: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Coding sequence array

Fig. 1.13

say, with chemotherapeutic

Page 11: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Coding sequence array

Fig. 1.13

Page 12: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Coding sequence array

Fig. 1.13

Page 13: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Coding sequence array

Fig. 1.13

expression

expression

expressed

not expressed

Page 14: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Why measure expression of all genes at once?

Page 15: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

“Regulon” expression response

http://www.mcb.mcgill.ca/~hallett/GEP/Lecture2/Image17.gif

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(e.g. cortisol)

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“Regulon” expression response

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http://www2.kenyon.edu/Depts/BioEllipse/courses/biol114/Chap06/week08a_files/regulon.gif

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Finding regulatory response on a large scale

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Oligo expression array

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transcripts

(soybean component)

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Expression profiles

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Time since drug administered

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Expression profiles

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Time since drug administered

Time since drug administered

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Expression profiles

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Time since drug administered

Time since drug administered

Each color is a regulon, or “cluster,” of co-regulated genes

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Expression effects of cancer

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Cancer classification

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Cancer classification

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Histological classification is finicky: can we do better?

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Diagnosis via transcriptional profile

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Diagnosis via transcriptional profile

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transcripts

patient samples

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Diagnosis via transcriptional profile

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Diagnosis via transcriptional profileQuickTime™ and a

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Natural variation among “normals”

Two human chromosomes differ at ~1/1000 bases.

96% of these differences are not in protein-coding sequence.Why?

Page 31: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Two human chromosomes differ at ~1/1000 bases.

96% of these differences are not in protein-coding sequence.Most protein coding mutations are deleterious;appear but are culled by natural selection.

Natural variation among “normals”

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Natural variation among “normals”

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Natural variation among “normals”

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Genetic variation in mRNA levels

ORFTFTF

G

kinaseTF

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Genetic variation in mRNA levels

ORFTFTF

G

kinaseTF

Likely to be a complex trait.

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Many mRNA differences at once

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Page 37: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Linkage mapping of mRNA levels

“Black 6” mouse x “DBA” mouse

Page 38: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Linkage mapping of mRNA levels

“Black 6” mouse x “DBA” mouse

~10% mRNA levels significantly different

Page 39: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Linkage mapping of mRNA levels

“Black 6” mouse x “DBA” mouse

111 F2 progeny

Page 40: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Linkage mapping of mRNA levels

“Black 6” mouse x “DBA” mouse

111 F2 progeny

Microarrayeach F2 liver

Page 41: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Linkage mapping of mRNA levels

“Black 6” mouse x “DBA” mouse

111 F2 progeny

Microarrayeach F2 liver

Genotypeeach F2

Page 42: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Linkage mapping of mRNA levels

“Black 6” mouse x “DBA” mouse

111 F2 progeny

Microarrayeach F2 liver

Genotypeeach F2

Looking for linkage (coinheritance) between marker and mRNA level.

Page 43: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

Page 44: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

G

G

Page 45: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

G

G

Page 46: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

G

G One allele = high mRNA,the other = low mRNA

Page 47: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

Page 48: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

Page 49: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

mRNA level shows linkage to locus of polymorphic regulator(s).

Page 50: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Marker is linked to polymorphism in expression regulation cascade

ORFTFTF

G

kinaseTF

mRNA level shows linkage to locus of polymorphic regulator(s).

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Locally acting polymorphisms

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Locally acting polymorphisms

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Locally acting polymorphisms

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Polymorphism responsible for mRNA difference is at the locus of the gene itself

Page 54: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Locally acting polymorphisms

ORFTFTF

G

kinaseTF

Page 55: Office hours Wednesday 3-4pm 304A Stanley Hall Review session 5pm Thursday, Dec. 11 GPB100.

Locally acting polymorphisms

ORFTFTF

G

kinaseTF

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Locally acting polymorphisms

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Polymorphism responsible for mRNA difference is at the locus of the gene itself

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Locally acting polymorphisms

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Polymorphism responsible for mRNA difference is at the locus of the gene itself

~25% of varying mRNAs are caused by locally acting polymorphism

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Nonlocal polymorphisms

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Nonlocal polymorphisms

One polymorphism in a key regulator can affect a regulon: 100’s of related mRNAs.

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Clinical applications

“Black 6” mouse x “DBA” mouse

111 F2 progeny

Microarrayeach F2 liver

Genotypeeach F2

Measure fat pad each F2

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Clinical applications

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Clinical applications

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Colored curves = fat mass at different body locations

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Clinical applications

Finding polymorphism responsible for difference in macroscopic phenotype is hard

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Clinical applications

Finding polymorphism responsible for difference in macroscopic phenotype is hard

If mRNAs change too, can learn mechanism from known function of encoded proteins

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Clinical applications

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Clinical applications

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Clinical applications

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Clinical applications

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Counts allele 1/allele 2, casesCounts allele 1/allele 2, controls

= 1.5

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Clinical applications

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Clinical applications

Marker predicts quantitative expression level = association

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Can we map expression traits first, disease afterward?

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Linkage of human transcripts

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Linkage of human transcripts

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Association of human transcripts

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Association of human transcripts

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linkage (families)

assoc (unrelated)

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Association in multiple populations

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Han Chinese and Japanese

European-Americans in Utah

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Association in multiple populations

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