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Stochasticity in Gene Expression

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Intracellular particle numbers are often quite low: Genetic copy number and number of DNA transcription factor ... Circadian rhythms. Development. Repressilator ... – PowerPoint PPT presentation

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Title: Stochasticity in Gene Expression


1
Stochasticity in Gene Expression
  • Arjun Raj

2
Why consider stochasticity?
  • Intracellular particle numbers are often quite
    low
  • Genetic copy number and number of DNA
    transcription factor binding sites is very low.
  • RNA levels are also often quite low (lt100
    molecules per cell.
  • Consequences
  • Kinetic mass action equations may no longer be
    accurate, since they only really give information
    about the mean.
  • A more correct model may be a chemical master
    equation.

3
Master Equation
  • In practice, the master equation is not solvable
    in closed form for even moderately complicated
    systems.
  • One could possibly solve the resultant system of
    ODEs numerically
  • Unfortunately, the number of equations increases
    exponentially with the number of species.
  • Often, the only solution left is to compute a
    large number of sample paths and then measure the
    statistics.
  • Gillespies algorithm for generating sample paths
    is efficient and, amazingly, generates exact
    paths.

4
Modifications of Gillespies algorithm
  • By cleverly updating the propensities, one can
    reduce computation time of the first reaction
    method so that it is faster than the direct
    method.
  • Should the particle numbers be large enough that
    the propensities change by a relatively small
    amount, one can leap ahead in the time history of
    the system by assuming propensities are constant
    (?-leap method).
  • Should the particle numbers be even larger, one
    can replace the master equation with a
    Langevin-type equation.

5
Measurements of noise
  • Phenotypic variation is commonly observed in
    clonal populations.
  • Question how much of the noise is due to
    transcriptional noise and how much is due to
    translational noise?

6
Measurements in Bacillus subtilis
  • Experiments introduced GFP chromosomallly into B.
    subtilis under the control of a IPTG inducible
    promoter (Pspac), allowing for control of
    transcriptional efficiency.
  • Translational efficiency varied by altering RBS.

7
Results
  • Noise quantitated using Fano factor of
    ltp2gt/ltpgt.
  • Measures deviation from Poisson behavior.
  • Noise seems largely independent of
    transcriptional efficiency, but shows a linear
    correlation with translational efficiency.

8
Why linear behavior?
  • Can solve the chemical master equation using
    moment generating functions.
  • Results in ltrgt being kR/?R, obeying a Poisson
    distribution.
  • However, p obeys a different distribution

9
Situation appears to be different in eukaryotes
  • Contructed a more complicated genetic control
    mechanism in yeast.
  • Transcription mechanisms are different in
    eukaryotes, so might have different noise
    characteristics.

10
Results
  • Measured noise using Fano factor as a function of
    transcriptional efficiency by varying amount of
    galactose and Atc in growth medium.
  • Also varied translational efficiency by using
    different codon variants of yEGFP gene.

11
Simulations
  • Used a model involving preinitiation complexes.
  • Were able to reproduce data (with appropriate
    parameters).

12
Question how much is the stochasticity is really
due to the inherent randomness of transcription
and translation?
  • Randomness in gene expression may be due to
    extrinsic factors which arent related to the
    actual stochastic nature of genetic expression
  • Amount of RNAP, ribosomes
  • State of cell in cell cycle
  • State of degradation machinery
  • How can one distinguish this from the intrinsic
    noise due to the randomness in the fundamental
    chemistry of gene expression?

13
Results in E. coli
  • Inserted YFP and CFP into E. coli genome in
    identical way.
  • Can measure contributions of intrinsic and
    extrinsic noise by measuring relative CFP and YFP
    levels within a single cell.

14
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15
Results
16
Results
  • Shows a decrease in intrinsic noise as
    transcriptional efficiency increases.
  • Hard to compare to other studies, since noise is
    measured differently.

17
So what?
  • Noise has been shown to be important in switching
    behavior of ?-phage life cycle in E. coli.
  • Noise must be controlled by cells to produce
    reliable behavior
  • Circadian rhythms
  • Development

18
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