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2.4 Cell Processes
pair depending on the cell type and organism. If these errors occur within a gene, then they
can be manifested as a mutation in the phenotype due to a change resulting from the phys
ical, chemical, or structural properties of the resulting peptide or protein that is expressed
from that particular gene.
Such a change could affect one or more biological processes in the cell, which utilize
this particular protein, resulting in an ultimate distribution of related biological properties,
depending on the particular nature of the mutated protein. If this mutated DNA nucleo
tide sequence is propagated into another cellular generation, then this biological variation
will also be propagated, and if this cell happens to be a so-called germ cell of a multicellular
organism, then this mutation may subsequently be propagated into offspring through sexual
reproduction. Hence, selective pressures can bias the distribution of the genetic makeup in
a population of cells and organisms of subsequent generations resulting, over many, many
generations, in the evolution of that species of organism.
However, there is increasing evidence for some traits, which can be propagated to subse
quent cellular generations not through alteration of the DNA sequence of the genetic code
itself but manifested as functional changes to the genome. For example, modification of his
tone proteins that help to package DNA in eukaryotes can result in changes to the expression
of the associated gene in the region of the DNA packaged by these histones. Similarly, the
addition of methyl chemical groups to the DNA itself are known to affect gene expression,
but without changing the underlying nucleotide sequence. The study of such mechanisms is
called “epigenetics.” An important factor with many such epigenetic changes is that they can
be influenced by external environmental factors.
This concept, on the surface, appears to be an intriguing reversion back to redundant the
ories exemplified by the so-called Lamarckism, which essentially suggested erroneously that,
for example, if a giraffe stretched its neck to reach leaves in a very tall tree, then the offspring
from that giraffe in subsequent generations would have slightly longer necks. Although epi
genetics does not make such claims, it does open the door to the idea that what an organism
experiences in its environment may affect the level of expression of genes in subsequent
generations of cells, which can affect the behavior of those cells in sometimes very dra
matic ways.
This is most prominently seen in cellular differentiation. The term “differentiation” used
by biologists means “changing into something different” and is not to be confused with the
term used in calculus. This is the process by which nongerm cells (i.e., cells not directly
involved in sexual reproduction, also known as somatic cells) turn into different cell types;
these cells all have the same DNA sequence, but there are significant differences in the timing
and levels of gene expressions between different cell types, now known to be largely due to
epigenetics modifications. This process is first initiated from the so-called stem cells, which
are cells that have not yet differentiated into different cell types. The reason why stem cells
have such current interest in biomedical applications is that if environmental external phys
ical and chemical triggers can be designed to cause stem cells to controllably and predictably
change into specific cell types, then these can be used to replace cells in damaged areas of the
body to repair specific physiological functions in humans, for example.
The exact mechanisms of natural selection, and ultimately species evolution, are not
clear. Although at one level, natural selection appears to occur at the level of the whole
organism, on closer inspection, a similar argument could be made at both larger and smaller
length scales. For example, at larger length scales, there is natural selection at the level of
populations of organisms, as exhibited in the selfless behavior of certain insects in appearing
to sacrifice their own individual lives to improve the survival of the colony as a whole. At a
smaller length scale, there are good arguments to individual cells in the same tissue com
peting with each other for nutrients and oxygen, and at a smaller length scale, still an argu
ment for completion occurring at the level of single genes (for a good background to the
debate, see Sterelny, 2007).
An interesting general mechanism is one involving the so-called emergent structures, a
phenomenon familiar to physicists. Although the rules of small length and time scale inter
action, for example, at the level of gene expression and the interactions between proteins, can
be reduced to relatively simple forces, these interactions can lead to higher-order structures