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adaptive sampling algorithm for the exploration of RNA mutational landscapes under evolutionary pressure Jérôme Waldispühl, PhD School of Computer Science, McGill Centre for Bioinformatics, McGill University, Canada Yann Ponty, PhD Laboratoire d’informatique (LIX), École Polytechnique, France

Jérôme Waldispühl, PhD School of Computer Science, McGill Centre for Bioinformatics,

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An unbiased adaptive sampling algorithm for the exploration of RNA mutational landscapes under evolutionary pressure. Jérôme Waldispühl, PhD School of Computer Science, McGill Centre for Bioinformatics, McGill University , Canada Yann Ponty , PhD Laboratoire d’informatique (LIX), - PowerPoint PPT Presentation

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Page 1: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

An unbiased adaptive sampling algorithm for the exploration of RNA mutational landscapes under evolutionary pressure

Jérôme Waldispühl, PhDSchool of Computer Science, McGill Centre for Bioinformatics,McGill University, Canada

Yann Ponty, PhDLaboratoire d’informatique (LIX),École Polytechnique, France

Page 2: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Philippe Flajolet (1948 – 2011)

Page 3: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

RNAmutants: Algorithms to explore the RNA mutational landscape

Overview

Understanding how mutations influence RNA secondary structures AND how structures influence mutations (Waldispühl et al., PLoS Comp Bio, 2008).

Page 4: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Sampling k-mutants

CAGUGAUUGCAGUGCGAUGC (-1.20)..((.(((((...))))))) Classic: 0 mutation

CAGUGAUUGCAGUGCGAUcC (-3.40)..(.((((((...)))))))CAGUGAUUGCAGUGCGgUGC (-0.30)((.((....)).))......CAGUGAUcGCAGUGCGAUGC (-3.10).....(((((...)))))..

RNAmutants: 1 mutation

uAGcGccgGgAGacCGgcGC (-18.00)..(((((((....)))))))CccUGgccGCAagGCcAgGg (-20.40)((((((((....))))))))CcGUGgccGCgagGCcAcGg (-19.10)((((((((....))))))))

RNAmutants: 10 mutations

Seed

Sample k mutations increasing the folding energyConsequence: it increases the C+G content

Page 5: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Objectives

How to efficiently sample sequences at arbitrary C+G contents … without bias!

C+G Content (%)

Sam

ple

frequ

ency

Target C+G content

Page 6: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Outline

• Background: RNAmutants in a nutshell Algorithms to sample RNA secondary structures and mutations.

• Our approach: Adaptive sampling Uniformly shifting the distribution of samples.

• Results: Evolutionary studies Insights on the evolutionary pressure stemming from an optimization of the thermodynamical stability.

Page 7: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Outline

• Background: RNAmutants in a nutshell Algorithms to sample RNA secondary structures and mutations.

• Our approach: Adaptive sampling Uniformly shifting the distribution of samples.

• Results: Evolutionary studies Insights on the evolutionary pressure stemming from an optimization of the thermodynamical stability.

Page 8: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

RNA secondary structure

The secondary structure is the ensemble of base-pairs in the structure.

Bracket notation:((((((((…)))..((((….)))).(((…)))..)))))

Page 9: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Loop decomposition

Stacking pairs

Page 10: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

UUUACGGCUAGC

Parameterization of the mutational landscape

UCUGAAACCCGU

UUUACGGCCAGC

Sequence ensemble Structure ensemble

CCUCAACGAAGC

UCUACGGCCAGC

UUUAAGGCCAGC

1-neighborhood(1 mutations)

Page 11: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Classical Recursions (Zuker & Stiegler, McCaskill)

Enumerate all secondary structures

Page 12: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

RNAmutants Generalize Classical Algorithms

Enumerate all secondary structures over all mutants (Waldispuhl et al., ECCB, 2002)

Page 13: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Our approach

Explore the complete mutation landscape. Polynomial time and space algorithm. Compute the partition function for all sequences:

Sample by backtracking the dynamic prog. tables.

RNAmutants

(Waldispuhl et al., PLoS Comp Bio, 2008)

Z = exp(− E(s,S)RT

)S∑

s∑

Z(s) = exp(β ⋅E(s,S))S

RNAmutants:

Single sequence:

Page 14: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Sampling k-mutants

CAGUGAUUGCAGUGCGAUGC (-1.20)..((.(((((...))))))) Classic: 0 mutation

CAGUGAUUGCAGUGCGAUcC (-3.40)..(.((((((...)))))))CAGUGAUUGCAGUGCGgUGC (-0.30)((.((....)).))......CAGUGAUcGCAGUGCGAUGC (-3.10).....(((((...)))))..

RNAmutants: 1 mutation

uAGcGccgGgAGacCGgcGC (-18.00)..(((((((....)))))))CccUGgccGCAagGCcAgGg (-20.40)((((((((....))))))))CcGUGgccGCgagGCcAcGg (-19.10)((((((((....))))))))

RNAmutants: 10 mutations

Seed

Sample k mutations increasing the folding energyConsequence: it increases the C+G content

Page 15: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Outline

• Background: RNAmutants in a nutshell Algorithms to sample RNA secondary structures and mutations.

• Our approach: Adaptive sampling Uniformly shifting the distribution of samples.

• Results: Evolutionary studies Insights on the evolutionary pressure stemming from an optimization of the thermodynamical stability.

Page 16: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

UUUAAGGCUAGC

Our approach: Weighting mutations

UCUGAAACCCGU

UUUAAGGCCAGC

Sequence ensemble Structure ensemble

CCUCAACGAAGC

UAUAAGGCCAGC

UUUAGGGCCAGC

w-1

1w Z

w-1. ZC9U

1. ZU2A

w. ZA5GWeighted by

partition function value

Promote A+U content

Penalize C+G content

No change

Page 17: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Weighting recursive equations

) × W(i,x) × W(j,y)(

× W(j,y)

W (i,x) =w If A,U →C,Gw−1 If C,G→ A,U1 Otherwise

⎧ ⎨ ⎪

⎩ ⎪

Page 18: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

C+G Content (%)

Effect of weighted sampling

Unweighted sampling weighted (w=1/2) weighted (w=2)

Freq

uenc

y of

sa

mpl

es

Page 19: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Sampling pipe-line

• Keep all samples at the target C+G and reject others.• Update w at each iteration using a bisection method.• Stop when enough samples have been stored.

Page 20: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Some features

• After rejection, the weighted schema only impact the performance, not the probability. This is unbiased.

• Partition function can be written as a polynom:

After n iterations we can to calculate all ai and inverse the polynom to compute the optimal weight w.

Remark: In practice, less interations are necessary€

Z = ai ⋅w ii= 0

n

Page 21: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Example: 40 nt., 10000 samples, 30 mutations, 70% C+G content

Cumulative distribution

Page 22: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Outline

• Background: RNAmutants in a nutshell Algorithms to sample RNA secondary structures and mutations.

• Our approach: Adaptive sampling Uniformly shifting the distribution of samples.

• Results: Evolutionary studies Insights on the evolutionary pressure stemming from an optimization of the thermodynamical stability.

Page 23: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

20 nucleotides 40 nucleotides

Low C+G-contents favor structural diversity

Simulation at fixed G+C content from random seeds

10% 30% 50% 70% 90%

Page 24: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Low C+G contents favor internal loop insertion

10% 30% 50% 70% 90%

Num

ber o

f Int

erna

l Loo

ps

Page 25: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

20 nucleotides 40 nucleotides

High G+C-contents reduce evolutionary accessibility

Simulation at fixed G+C content from random seeds

10% 30% 50% 70% 90%

Page 26: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Perspectives

• More studies of Sequence-Structure maps.• Applications to RNA design.• Same techniques can be applied to other parameters (e.g. number of base pairs).• Can be generalized to multiple parameters.

Page 27: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Acknowledgments

Ecole Polytechnique• Jean-Marc SteyaertBoston College• Peter Clote

INRIA• Philippe FlajoletMIT• Bonnie Berger• Srinivas Devadas• Mieszko Lis• Alex Levin• Charles W. O’DonnellGoogle Inc.• Behshad Behzadi

Yann PontyCNRS at LIX, École Polytechnique, France.

University of Paris 6• Olivier BodiniUniversity of Paris 11• Alain Denise

Page 28: Jérôme Waldispühl, PhD School of Computer Science,  McGill Centre for Bioinformatics,

Would you like to know more?

O. Bodini, and Y. PontyMulti-dimensional Boltzmann Sampling of Languages,Proceedings of AOFA'10, 49--64, 2010

J. Waldispühl, S. Devadas, B. Berger and P. Clote,Efficient Algorithms for Probing the RNA Mutation Landscape,Plos Computational Biology, 4(8):e1000124, 2008.

http://csb.cs.mcgill.ca/RNAmutants