algorithms in biology molecular organization und evolutionpks/presentation/linz-06.pdf27.8 h = 1.16...
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![Page 1: Algorithms in Biology Molecular Organization und Evolutionpks/Presentation/linz-06.pdf27.8 h = 1.16 d 6.94 d 115.7 d 1.90 a 3.17 a 19.01 a Bacteria 20 min 10 h 138.9 d 11.40 a 38.03](https://reader031.vdocuments.us/reader031/viewer/2022041623/5e401c4ee30afa71ed212db0/html5/thumbnails/1.jpg)
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Algorithms in Biology
Molecular Organization und Evolution
Peter Schuster
Institut für Theoretische Chemie, Universität Wien, Austriaand
The Santa Fe Institute, Santa Fe, New Mexico, USA
Algorithmen des Lebens
Lentos Kunstmuseum, Linz, 30.05.2006
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Web-Page for further information:
http://www.tbi.univie.ac.at/~pks
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Algorithm = A rule of procedure for solving a (mathematical) problem in a finite number of steps that frequently involves repetition of an operation.
Webster’s New Encyclopedic Dictionary, Black Dog & Levinthal Publishers Inc., New York 1995.
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Nothing in biology makes sense except in the light of evolution.
Theodosius Dobzhansky, 1973.
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Genotype, Genome
Phenotype
Unf
oldi
ng o
f th
e ge
noty
pe
Highly specific environmental conditions
Developmental program
Collection of genes
Evolution explainsthe origin of species and
their interactions
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Three necessary conditions for Darwinian evolution are:
1. Multiplication,
2. Variation, and
3. Selection.
Variation through mutation and recombination operates on the genotype whereas the phenotype is the target of selection.
One important property of the Darwinian scenario is that variations in the form of mutations or recombination events occur uncorrelated with their effects on the selection process.
All conditions can be fulfilled not only by cellular organisms but also bynucleic acid molecules in suitable cell-free experimental assays.
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The holism versus reductionism debate
The reductionists’ program
Molecular biologists perform a bottom-up approach to interpret biological phenomena by the methods of chemistry and physics.
The holistic approach
Macroscopic biologists aim at a top-down approach to describe the phenomena observed in biology.
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What should be the attitude of a biologist working on whole organisms to molecular biology? It is, I think, foolish to argue that we (the macroscopic biologists)are discovering things that disprove molecular biology. It would be more sensible to say to molecular biologists that there are phenomena that they will one day have to interpret in their terms.
John Maynard Smith, The problems of biology. Oxford University Press, 1986.
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Genotype, Genome
Genetic informationGCGGATTTAGCTCAGTTGGGAGAGCGCCAGACTGAAGATCTGGAGGTCCTGTGTTCGATCCACAGAATTCGCACCA
Phenotype
Unf
oldi
ng o
f th
e ge
noty
pe
Highly specific environmental conditions
James D. Watson undFrancis H.C. Crick
Biochemistrymolecular biologystructural biology
molecular evolutionmolecular genetics
systems biology bioinfomatics
Hemoglobin sequenceGerhard Braunitzer
The exciting RNA story
Evolution of RNA molecules,ribozymes and splicing,
the idea of an RNA world,selection of RNA molecules,
RNA editing,the ribosome is a ribozyme,
small RNAs and RNA switches.
Omics‘The new biology is
the chemistry ofliving matter’
Molecular evolutionLinus Pauling andEmile Zuckerkandl
ManfredEigen
Max Perutz
John Kendrew
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E. coli: Length of the Genome 4×106 NucleotidesNumber of Cell Types 1Number of Genes 4 000
Man: Length of the Genome 3×109 NucleotidesNumber of Cell Types 200Number of Genes 40 000 - 60 000
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A B C D E F G H I J K L
1 Biochemical Pathways
2
3
4
5
6
7
8
9
10
The reaction network of cellular metabolism published by Boehringer-Ingelheim.
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The citric acid or Krebs cycle (enlarged from previous slide).
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The spatial structure of the bacterium Escherichia coli
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Structural biology
Proteins, nucleic acids, supramolecular complexes,
molecular machines
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Three-dimensional structure of thecomplex between the regulatoryprotein cro-repressor and the bindingsite on -phage B-DNA
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OCH2
OHO
O
PO
O
O
N1
OCH2
OHO
PO
O
O
N2
OCH2
OHO
PO
O
O
N3
OCH2
OHO
PO
O
O
N4
N A U G Ck = , , ,
3' - end
5' - end
Na
Na
Na
Na
5'-end 3’-endGCGGAU AUUCGCUUA AGUUGGGA G CUGAAGA AGGUC UUCGAUC A ACCAGCUC GAGC CCAGA UCUGG CUGUG CACAG
Definition of RNA structure
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The Vienna RNA package
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RNA sequence
RNA structureof minimal free
energy
RNA folding:
Structural biology,spectroscopy of biomolecules, understanding
molecular functionEmpirical parameters
Biophysical chemistry: thermodynamics and
kinetics
Sequence, structure, and design
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RNA sequence
RNA structureof minimal free
energy
RNA folding:
Structural biology,spectroscopy of biomolecules, understanding
molecular function
Inverse FoldingAlgorithm
Iterative determinationof a sequence for the
given secondarystructure
Sequence, structure, and design
Inverse folding of RNA:
Biotechnology,design of biomolecules
with predefined structures and functions
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UUUAGCCAGCGCGAGUCGUGCGGACGGGGUUAUCUCUGUCGGGCUAGGGCGC
GUGAGCGCGGGGCACAGUUUCUCAAGGAUGUAAGUUUUUGCCGUUUAUCUGG
UUAGCGAGAGAGGAGGCUUCUAGACCCAGCUCUCUGGGUCGUUGCUGAUGCG
CAUUGGUGCUAAUGAUAUUAGGGCUGUAUUCCUGUAUAGCGAUCAGUGUCCG
GUAGGCCCUCUUGACAUAAGAUUUUUCCAAUGGUGGGAGAUGGCCAUUGCAG
Minimum free energycriterion
Inverse folding
1st2nd3rd trial4th5th
The inverse folding algorithm searches for sequences that form a given RNA secondary structure under the minimum free energy criterion.
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Reference for postulation and in silico verification of neutral networks
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RNA secondary structures derived from a single sequence
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Reference for the definition of the intersection and the proof of the intersection theorem
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A ribozyme switch
E.A.Schultes, D.B.Bartel, Science 289 (2000), 448-452
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Two ribozymes of chain lengths n = 88 nucleotides: An artificial ligase (A) and a natural cleavage ribozyme of hepatitis- -virus (B)
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The sequence at the intersection:
An RNA molecules which is 88 nucleotides long and can form both structures
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Two neutral walks through sequence space with conservation of structure and catalytic activity
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Generation time
Selection and adaptation
10 000 generations
Genetic drift in small populations 106 generations
Genetic drift in large populations 107 generations
RNA molecules 10 sec 1 min
27.8 h = 1.16 d 6.94 d
115.7 d 1.90 a
3.17 a 19.01 a
Bacteria 20 min 10 h
138.9 d 11.40 a
38.03 a 1 140 a
380 a 11 408 a
Multicelluar organisms 10 d 20 a
274 a 200 000 a
27 380 a 2 × 107 a
273 800 a 2 × 108 a
Time scales of evolutionary change
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Evolution of RNA molecules based on Qβ phage
D.R.Mills, R.L.Peterson, S.Spiegelman, An extracellular Darwinian experiment with a self-duplicating nucleic acid molecule. Proc.Natl.Acad.Sci.USA 58 (1967), 217-224
S.Spiegelman, An approach to the experimental analysis of precellular evolution. Quart.Rev.Biophys. 4 (1971), 213-253
C.K.Biebricher, Darwinian selection of self-replicating RNA molecules. Evolutionary Biology 16 (1983), 1-52
G.Bauer, H.Otten, J.S.McCaskill, Travelling waves of in vitro evolving RNA.Proc.Natl.Acad.Sci.USA 86 (1989), 7937-7941
C.K.Biebricher, W.C.Gardiner, Molecular evolution of RNA in vitro. Biophysical Chemistry 66 (1997), 179-192
G.Strunk, T.Ederhof, Machines for automated evolution experiments in vitro based on the serial transfer concept. Biophysical Chemistry 66 (1997), 193-202
F.Öhlenschlager, M.Eigen, 30 years later – A new approach to Sol Spiegelman‘s and Leslie Orgel‘s in vitro evolutionary studies. Orig.Life Evol.Biosph. 27 (1997), 437-457
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Genotype = Genome
GGCUAUCGUACGUUUACCCAAAAAGUCUACGUUGGACCCAGGCAUUGGAC.......GMutation
Fitness in reproduction:
Number of genotypes in the next generation
Unfolding of the genotype:
RNA structure formation
Phenotype
Selection
Evolution of phenotypes: RNA structures and replication rate constants
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Complementary replication is thesimplest copying mechanism of RNA.Complementarity is determined byWatson-Crick base pairs:
G C and A=U
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RNA sample
Stock solution: Q RNA-replicase, ATP, CTP, GTP and UTP, buffer
Time0 1 2 3 4 5 6 69 70
The serial transfer technique applied to RNA evolution in vitro
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Reproduction of the original figure of theserial transfer experiment with Q RNAβ
D.R.Mills, R,L,Peterson, S.Spiegelman,
. Proc.Natl.Acad.Sci.USA (1967), 217-224
An extracellular Darwinian experiment with a self-duplicating nucleic acid molecule58
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Decrease in mean fitnessdue to quasispecies formation
The increase in RNA production rate during a serial transfer experiment
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Evolution in silico
W. Fontana, P. Schuster, Science 280 (1998), 1451-1455
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Replication rate constant:
fk = / [ + dS(k)]
dS(k) = dH(Sk,S )
Selection constraint:
Population size, N = # RNA molecules, is controlled by
the flow
Mutation rate:
p = 0.001 / site replication
NNtN ±≈)(
The flowreactor as a device for studies of evolution in vitro and in silico
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S{ = ( )I{
f S{ {ƒ= ( )
S{
f{
I{M
utat
ion
Genotype-Phenotype Mapping
Evaluation of the
Phenotype
Q{jI1
I2
I3
I4 I5
In
Q
f1
f2
f3
f4 f5
fn
I1
I2
I3
I4
I5
I{
In+1
f1
f2
f3
f4
f5
f{
fn+1
Q
Evolutionary dynamics including molecular phenotypes
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Phenylalanyl-tRNA as target structure
Randomly chosen initial structure
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In silico optimization in the flow reactor: Evolutionary Trajectory
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Evolutionary design of RNA molecules
D.B.Bartel, J.W.Szostak, In vitro selection of RNA molecules that bind specific ligands. Nature 346 (1990), 818-822
C.Tuerk, L.Gold, SELEX - Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase. Science 249 (1990), 505-510
D.P.Bartel, J.W.Szostak, Isolation of new ribozymes from a large pool of random sequences. Science 261 (1993), 1411-1418
R.D.Jenison, S.C.Gill, A.Pardi, B.Poliski, High-resolution molecular discrimination by RNA. Science 263 (1994), 1425-1429
Y. Wang, R.R.Rando, Specific binding of aminoglycoside antibiotics to RNA. Chemistry & Biology 2 (1995), 281-290
Jiang, A. K. Suri, R. Fiala, D. J. Patel, Saccharide-RNA recognition in an aminoglycoside antibiotic-RNA aptamer complex. Chemistry & Biology 4 (1997), 35-50
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Evolutionary design by selection
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A SELEX experiment optimizing binding affinities
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additional methyl group
Dissociation constants and specificity of theophylline, caffeine, and related derivatives of uric acid for binding to a discriminating aptamer TCT8-4
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Schematic drawing of the aptamer binding site for the theophylline molecule
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The three-dimensional structure of the tobramycin aptamer complex
L. Jiang, A. K. Suri, R. Fiala, D. J. Patel, Chemistry & Biology 4:35-50 (1997)
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Acknowledgement of support
Fonds zur Förderung der wissenschaftlichen Forschung (FWF)Projects No. 09942, 10578, 11065, 13093
13887, and 14898
Wiener Wissenschafts-, Forschungs- und Technologiefonds (WWTF) Project No. Mat05
Jubiläumsfonds der Österreichischen NationalbankProject No. Nat-7813
European Commission: Contracts No. 98-0189, 12835 (NEST)
Austrian Genome Research Program – GEN-AU: BioinformaticsNetwork (BIN)
Österreichische Akademie der Wissenschaften
Siemens AG, Austria
Universität Wien and the Santa Fe Institute
Universität Wien
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Coworkers
Peter Stadler, Bärbel M. Stadler, Universität Leipzig, GE
Jord Nagel, Kees Pleij, Universiteit Leiden, NL
Walter Fontana, Harvard Medical School, MA
Christian Reidys, Christian Forst, Los Alamos National Laboratory, NM
Ulrike Göbel, Walter Grüner, Stefan Kopp, Jaqueline Weber, Institut für Molekulare Biotechnologie, Jena, GE
Ivo L.Hofacker, Christoph Flamm, Andreas Svrček-Seiler, Universität Wien, AT
Kurt Grünberger, Michael Kospach, Andreas Wernitznig, Stefanie Widder, Michael Wolfinger, Stefan Wuchty, Universität Wien, AT
Jan Cupal, Stefan Bernhart, Lukas Endler, Ulrike Langhammer, Rainer Machne, Ulrike Mückstein, Hakim Tafer, Thomas Taylor, Universität Wien, AT
Universität Wien
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Web-Page for further information:
http://www.tbi.univie.ac.at/~pks
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