Biochemistry and molecular biology have been focusing
on the structural, catalytic, and regulatory properties
of individual macromolecules from the perspective
of clarifying the mechanisms of metabolism and
gene expression. Complete genomes of ‘primitive’
living organisms seem to be substantially larger than
necessary for metabolism and gene expression alone.
This is in line with the findings of silent phenotypes for
supposedly important genes, apparent redundancy of
functions, and variegated networks of signal transduction
and transcription factors. Here we propose
that evolutionary optimization has been much more intensive
than to lead to the bare minima necessary for
autonomous life. Much more complex organisms prevail.
Much of this complexity arises in the nonlinear
interactions between cellular macromolecules and in
subtle differences between paralogs (isoenzymes).
The complexity can only be understood when analyzed
quantitatively, for which quantitative experimentation
is needed in living systems that are as simple
and manipulatable as possible, yet complex in the
above sense. We illustrate this for the glutamine synthetase
cascade in
Print ISSN: 1431-6730
Volume: 381, 09/2000
Pages: 965 - 972