A startling discovery of enormous implication has just been
reported in the premier research journal, Science.
Despite the accepted dogma that all of a person's cells have the same
genetic coding, it turns out that this is not true, especially in neurons. The DNA
in each nerve cell (we don't know about sex cells) has hundreds of mutations of
the A-T, C-G nucleotides that constitute the genetic code for the neuron. Thus,
no two neurons are alike. The study was conducted by 18 research teams at 15
U.S. institutions, formed as a consortium by the National Institute of Mental
Health to examine neural genetic coding, using repositories of postmortem brain
tissue taken from both healthy people and those with various mental diseases.
The scientists have no explanation
at present for what is causing so many mutations and why each neuron has a
different genetic profile. The most obvious possibility might seem to be that
the mutations occurred as transcription errors during cell division. But there
is a major problem with this explanation. We don't know when these mutations occurred. Except for granule cells in the
hippocampus and cerebellum, neurons generally do not divide after the first few
days after birth. So, if cell division is the cause of mutations, it must be due
to what happens during the early post-natal period.
If the mutations occurred
sporadically throughout a lifetime, a likely cause for mutation might be DNA
damage caused by the free radicals that are generated in ordinary metabolism. Environmental
toxins are another possible cause. The point is that the DNA changes are likely
to affect how a neuron functions, and that change can last a lifetime.
We know that mutations can cause
brain cancer and even certain other brain diseases. The research consortium was
commissioned to see if the genetic variants predisposed to neuropsychiatric
disease. Obviously, the vast majority of people have these diverse genetic
codes in their neurons that do not cause disease. What do they cause? Can the
mutations affect which neurons participate in which circuits? Can mutations
affect how well you reason, or memorize, or your emotional responsivity? Nobody
knows.
A whole new field of research has
now been opened. Scientists need to examine different neuronal cell types to
see if they are equally affected by mutation. Obvious comparisons needed are
between granule cells and all the other neuron types that do not divide.
There is a related aspect that is
not considered in this context. That is the likelihood that each neuron differs
not only in its genetic code, but also in which genes are expressed. The new
field of "epigenetics" has revealed that environmental influences,
ranging from drugs, toxins, metabolites, and perhaps even lifestyles can affect
the expression of genes, even when there is no mutation. In the case of brain,
there is the distinct possibility that one's mental life can affect gene
expression. This needs to be studied.
So far, what I have said about gene
change and expression refers to single individuals. But what if some of these
gene mutations or epigenetic effects that occur in neurons also occur in sex
cells? That would mean that traits acquired during one's lifetime could be
passed on to future generations. I would hope that the research consortium that
has made this monumental discovery about brain cells will extend its charter to
also examine sperm and ova.
Recent research on the genetics of
the classic animal model of brain function, C.
elegans, reveals that epigenetic inheritance of neuronal traits does occur.
Gene expression was modified by exposing the animals to high temperatures, and
the genetic change was conveyed via both ova and sperm to offspring that had no
exposure to high temperature. The epigenetic change was still present some 5-14
generations later.
To the extent that the findings of
both of these studies can be extrapolated to humans, we must now consider the
possibility that personal lifestyle, environmental, and cultural influences on people
may be propagated to successive generations of their children. Bad environments
and lifestyle choices may extend well into the future, magnifying the
deleterious consequences through multiple generations. We now have to consider
that medical and behavioral problems, poverty, and degenerate cultures can arise
not only when people make poor choices but that the effects can be genetically propagated
to subsequent generations.
These issues may seem to present a
challenge to the notion that humans have free will. We are programmed by things
that happen to us. But do we not have a choice in deciding much of what we
expose ourselves to? The issues are explored in my recent book, Making a Scientific Case for Conscious
Agency and Free Will (Academic Press).
Sources:
McConnell, M. J. et al. (2017).Intersection of diverse
neuronal genomes and neuropsychiatric diseases: The brain somatic mosaicism
network. Science. 356(6336), 395. doi:
10.1126/scienceaa1641.
Klosin, Adam et al. (2017). Transgenerational transmission
of environmental information in C. elegans. Science. 356 (6335), 320-323.
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