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Towards Quantitative Biology<br />

Robin Friedman


ATG ACG AAG...<br />

Methionine<br />

Lysine<br />

Threonine<br />

DNA<br />

mRNA<br />

<strong>Protein</strong>


ATG ACG AAG...<br />

Methionine<br />

Lysine<br />

Threonine<br />

DNA<br />

DNA<br />

DNA<br />

mRNA<br />

mRNA<br />

mRNA<br />

<strong>Protein</strong><br />

<strong>Protein</strong><br />

<strong>Protein</strong>


ATG ACG AAG...<br />

Methionine<br />

Lysine<br />

Threonine<br />

DNA<br />

DNA<br />

DNA<br />

mRNA<br />

mRNA<br />

mRNA<br />

<strong>Protein</strong><br />

<strong>Protein</strong><br />

<strong>Protein</strong><br />

One gene One protein One function


Number of genes<br />

Organismal complexity


Species<br />

Number of Neurons Number of genes<br />

Human 10 11 21,000<br />

Mouse 10 7 22,000<br />

Fruitfly 10 5 14,000<br />

Nematode 302 19,000


Species<br />

Number of Neurons Number of genes<br />

Human 10 11 21,000<br />

Mouse 10 7 22,000<br />

Fruitfly 10 5 14,000<br />

Nematode 302 19,000


Species<br />

Number of Neurons Number of genes<br />

Human 10 11 21,000<br />

Mouse 10 7 22,000<br />

Fruitfly 10 5 14,000<br />

Nematode 302 19,000<br />

1.5% of human genome is protein coding


Nucleus<br />

Cytoplasm<br />

DNA<br />

pre-mRNA<br />

transcription<br />

<strong>Protein</strong><br />

splicing<br />

mRNA<br />

translation<br />

export<br />

degradation


Nucleus<br />

Cytoplasm<br />

DNA<br />

pre-mRNA<br />

transcription<br />

<strong>Protein</strong><br />

mRNA<br />

splicing<br />

translation<br />

miRNAs<br />

export<br />

degradation


Transcription<br />

Factors<br />

RNA Binding<br />

<strong>Protein</strong>s<br />

mRNAs<br />

miRNAs


Transcription<br />

Factors<br />

RNA Binding<br />

<strong>Protein</strong>s<br />

mRNAs<br />

miRNAs


Transcription<br />

Factors<br />

RNA Binding<br />

<strong>Protein</strong>s<br />

mRNAs<br />

miRNAs


Sequencing cost (nucleotides/dollar)<br />

10 6<br />

10 4<br />

10 2<br />

10 0<br />

10 6<br />

10 4<br />

10 2<br />

10 0<br />

Storage cost (megabytes/dollars)<br />

1990 1995 2000 2005 2010<br />

Year


Transcription<br />

Factors<br />

RNA Binding<br />

<strong>Protein</strong>s<br />

mRNAs<br />

miRNAs


Electrophoretic mobility shift assay<br />

Bound DNA<br />

Unbound DNA<br />

Increasing protein concentration


Electrophoretic mobility shift assay<br />

Bound DNA<br />

Unbound DNA<br />

Increasing protein concentration


10 Gb per run<br />

Illumina Genome Analyzer


Illumina Genome Analyzer<br />

GCC AGA TTG<br />

>10 Gb per run


Illumina Genome Analyzer<br />

GCC AGA TTG<br />

A<br />

C<br />

G<br />

T<br />

>10 Gb per run


Illumina Genome Analyzer<br />

GCC AGA TTG<br />

A<br />

C<br />

G<br />

T<br />

>10 Gb per run


Illumina Genome Analyzer<br />

GCC AGA TTG<br />

A<br />

C<br />

G<br />

T<br />

>10 Gb per run


Illumina Genome Analyzer<br />

GCC AGA TTG<br />

A<br />

C<br />

G<br />

T<br />

>10 Gb per run


Illumina Genome Analyzer<br />

A channel


Illumina Genome Analyzer<br />

A channel<br />

C channel<br />

G channel<br />

T channel


Illumina Genome Analyzer<br />

A channel<br />

C channel<br />

Merge<br />

G channel<br />

T channel


HiTS-FLIP method<br />

High-Throughput Sequencing<br />

Fluorescent Ligand Interaction Profile<br />

100,000,000<br />

Random 25mers


HiTS-FLIP method<br />

High-Throughput Sequencing<br />

Fluorescent Ligand Interaction Profile<br />

100,000,000<br />

Random 25mers


HiTS-FLIP method<br />

High-Throughput Sequencing<br />

Fluorescent Ligand Interaction Profile<br />

100,000,000<br />

Random 25mers<br />

GCN4<br />

mOrange tag


HiTS-FLIP method<br />

High-Throughput Sequencing<br />

Fluorescent Ligand Interaction Profile<br />

100,000,000<br />

Random 25mers<br />

GCN4<br />

mOrange tag


GCN4<br />

HiTS-FLIP method


HiTS-FLIP method<br />

GCN4<br />

Merge


HiTS-FLIP method<br />

GCN4<br />

Merge


HiTS-FLIP method<br />

GCN4<br />

Merge


GCN4<br />

master regulator of amino<br />

acid biosynthesis in yeast


GCN4<br />

master regulator of amino<br />

acid biosynthesis in yeast<br />

Decades of research<br />

on binding specificity<br />

ATGACTCAT<br />

ATGAGTCAT


GCN4 binds its canonical motif<br />

440,000,000 data points


GCN4 binds its canonical motif<br />

Intensity above background<br />

0.9<br />

0.8<br />

0.7<br />

0.6<br />

0.5<br />

0.4<br />

0.3<br />

0.2<br />

0.1<br />

0<br />

440,000,000 data points<br />

7mers<br />

Consensus:<br />

TATGACTCAT<br />

NNTGACTCAN<br />

NATGACTCNN<br />

NNTGACTAAN<br />

NGTGACTCNN<br />

TATGACTNNN<br />

NATGACTANN<br />

NATGACTGNN<br />

NNNGACTCAT<br />

GATGACTNNN<br />

NATGACACNN<br />

NNNTACAGGT<br />

NNNAGCTACC<br />

NGATACTANN<br />

NNNTCCTAAC<br />

NATGAATGNN


Concentration-dependent GCN4 binding<br />

Normalized wash intensity above background<br />

0.9<br />

0.8<br />

0.7<br />

0.6<br />

0.5<br />

0.4<br />

0.3<br />

0.2<br />

0.1<br />

0<br />

−0.1<br />

1 10 100 1000<br />

[Gcn4p] (nM)<br />

Consensus:<br />

TATGACTCAT<br />

NNTGACTCAN<br />

NATGACTCNN<br />

NNTGACTAAN<br />

NGTGACTCNN<br />

TATGACTNNN<br />

NATGACTANN<br />

NATGACTGNN<br />

NNNGACTCAT<br />

GATGACTNNN<br />

NATGACACNN<br />

NNNTACAGGT<br />

NNNAGCTACC<br />

NGATACTANN<br />

NNNTCCTAAC<br />

NATGAATGNN


Dissociation constants<br />

Normalized wash intensity above background<br />

0.9<br />

0.8<br />

0.7<br />

0.6<br />

0.5<br />

0.4<br />

0.3<br />

0.2<br />

0.1<br />

0<br />

10 0 10 1 10 2 10 3<br />

[GCN4] (nM)<br />

Hill coefficient = 2.0<br />

KD = 42 nM


Dissociation constants<br />

1000<br />

HiTS−FLIP K D<br />

(nM)<br />

100<br />

10<br />

10 100 1000<br />

Gel shift K D<br />

(nM)<br />

R. Nutiu


Binding interdependencies<br />

TGACTCA<br />

TGAGTCT


Conclusion


Conclusion<br />

Colected a half billion data points, recapitulated<br />

decades of GCN4 research in a single experiment


Conclusion<br />

Colected a half billion data points, recapitulated<br />

decades of GCN4 research in a single experiment<br />

Opens door for more quantitative modeling of<br />

transcription


Acknowledgements<br />

Razvan Nutiu, Christopher Burge,<br />

Gary Schroth, Shujun Luo

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