Well I'd like to think as a 38 year old male my genome is
better than just shooting out a wad during my reproductive
years. In fact, men (I've read) can shoot out viable
reproductive wads quite late into their years although there
is a greater risk of mutation of sperm as age advances. With
women the situation is a little different (I've read) and
past the age of 40 there dramatically increased risks
regarding viable pregnancy and childbirth. (I hope the
moderator posts this because I'm tired of such statements,
"Following Richard Dawkins, we would like to reassert that
we indeed live as disposable somas, slaves of our germline
genome."😉 That's it the human race has little brains. Like a
maggot it lives to reproduce itself. This is true in
Darwinian terms but let us hope this remains not so.
I'd point out here that at least in medically advanced
Western nations longevity has increased. Yes, there are more
diseases after reproductive age but many are treatable and
this person can live to be 70, 80, etc. Are 70 and 80 year
old men disposable somas, slaves of the germline process?
I see possible validity, however, with the abstract's
statement, "Cancer and its relation to the TP53 gene may
offer a paradigmatic example. The observation that the
latency period in cancer can be prolonged in mice by
increasing the number of TP53 genes in their genome,
suggests that sooner or later we will have to address the
question of heritable disease avoidance via the manipulation
of the human germline."
Possibly with such gene therapy there is the possibility of
eliminating genetic diseases. Will we then live totally as
disposable somas, slaves of our germline genome? I'm
interested in the possible relationship between heritable
disease avoidance and genetic engineering. It would seem to
me this is a form of gene therapy by increasing the number
of TP53 genes in mice genomes. But there is the potential
maybe such heritable disease avoidance gene therapy may lead
to genetic engineering applications.
Michael Ragland
How good is our genome?
Group: sci.bio.evolution Date: Tue, Jun 29, 2004, 4:10pm
(EDT+4) From: [email hidden] (Robert Karl Stonjek)
How good is our genome? Philosophical Transactions:
Biological Sciences fobike://rsl/rtb January 29, 2004, vol.
359, no. 1441, pp. 95-98(4)
l/rtb/2004/00000359/00001441 Weill J-C.[1]; Radman M.[1]
[1] Faculte de Medecine Necker Enfants-Malades, Université
de Paris-V, Paris, France
Abstract: Our genome has evolved to perpetuate itself
through the maintenance of the species via an uninterrupted
chain of reproductive somas. Accordingly, evolution is not
concerned with diseases occurring after the soma's
reproductive stage. Following Richard Dawkins, we would like
to reassert that we indeed live as disposable somas, slaves
of our germline genome, but could soon start rebelling
against such slavery. Cancer and its relation to the TP53
gene may offer a paradigmatic example. The observation that
the latency period in cancer can be prolonged in mice by
increasing the number of TP53 genes in their genome,
suggests that sooner or later we will have to address the
question of heritable disease avoidance via the manipulation
of the human germline. Keywords: evolution; germline
modification; cancer; latency; p53 Document Type: Research
article ISSN: 0962-8436 DOI (article):
10.1098/rstb.2003.1369 SICI (online): 0962-8436(20040129)359:1441L.95;1-
Publisher: Royal Society
--
Posted by Robert Karl Stonjek.
"It's uncertain whether intelligence has any long term
survival value." Stephen Hawking