Researchers simulate molecular biological clock, New York University

Researchers at New York University have developed a model of the intra-cellular mammalian biological clock that reveals
how rapid interaction of molecules with DNA is necessary for producing reliable 24-hour rhythms. They also found that without
the inherent randomness of molecular interactions within a cell, biological rhythms may dampen over time. These findings
appeared in the most recent issue of the Proceedings of the National Academy of Sciences (PNAS).


Daniel Forger, an NYU biologist and mathematician, and Charles Peskin, a professor at NYU's Courant Institute of Mathematical
Sciences and Center for Neural Science, developed a mathematical model of the biological clock that replicates the hundreds
of clock-related molecular reactions that occur within each mammalian cell.


Biological circadian clocks time daily events with remarkable accuracy--often within a minute each day. However,
understanding how circadian clocks function has proven challenging to researchers. This is partly because the 24-hour rhythm
is an emergent property of a complex network of many molecular interactions within a cell. Another complication is that
molecular interactions are inherently random, which raises the question how a clock with such imprecise components can keep
time so precisely. One way to combat molecular noise is to have large numbers of molecular interactions, but this is limited
by the small numbers of molecules of some molecular species within the cell (for instance, there are only two copies of DNA).



To simulate the random nature of the biochemical interactions of the mammalian intra-cellular circadian clock, Forger and
Peskin used the existing Gillespie method. The method tracks the changes in the integer numbers of each type of molecule of
the system as these biochemical reactions occur. Modeling each type of molecule separately helped avoid mathematical
assumptions in their model that may not be valid in real-life cells. Their model was validated with a large library of data
on the concentrations of the molecular species within the mouse molecular clock at different times of the day and data on the
behavior of mice with circadian clock mutations.


The results of their computer simulations showed that reliable 24-hour timekeeping can only be achieved if the regulatory
molecules that influence gene expression bind and unbind to DNA quickly--typically, within a minute. In this way, the large
number of bindings and unbindings helps to compensate for the small numbers of molecules involved. The researchers also found
that having more molecules in the cell does not necessarily lead to more accurate timekeeping. Removing all the CRY1
molecules (CRY1 mutant) or removing all the CRY2 molecules (CRY2 mutant), while keeping all other molecular species
unchanged, leads to more accurate timekeeping. While simulating the PER2 mutation, they found that circadian oscillations
could only be sustained in the presence of molecular noise. This may help explain some of the conflicting experimental
reports about the PER2 mutant.


"Without the rapidity of molecular interactions within these cells, the precision of the biological clock would be lost,"
explained Forger. "It is remarkable that a process occurring on the time scale of minutes can have such a profound effect on
one that occurs over 24 hours."


James Devitt

jamesvittnyu

New York University