Cheating -- and getting away with it
We would all like to believe that there is a kind of karma in
life that guarantees those who cheat eventually pay for their bad behavior, if
not immediately, then somewhere down the line. But a study of a new gene in the
amoebaDictyostelium
discoideum suggests
that, at least for amoebae, it is possible to cheat and get away with it.
Scientists have found a gene that allows amoebae to pass on more than their
fair share of their genes but doesn't make them less fit in other ways.
The
experimental work was conducted by then graduate student Lorenzo Santorelli as
part of a collaboration between evolutionary biologists David C. Queller and
Joan E. Strassmann of Rice University and Gadi Shaulsky and Adam Kuspa of
Baylor College of Medicine. Santorelli has since moved to Oxford University and
his advisors to Washington University in St. Louis, where Queller is the
Spencer T. Olin Professor of Biology and Strassmann is a professor of biology,
both in Arts & Sciences.
The
cheat in question is putting more than your clone's fair share of cells into a
communal spore body, so that your genome dominates the next generation of
amoebae. The idea has always been that cheating clones pay a price in the form
of reduced evolutionary fitness in some other chapter of their lives.
In work described in the Jan. 9 issue of BMC Evolutionary Biology, the scientists tested
the fitness of a knockout mutant (an amoeba with one disabled gene) called
CheaterB. When mixed with equal parts of a wild-type clone, the cheater clone
contributed almost 60 percent of the cells in the spore body, 10 percent more
than its fair share.
The
scientists ran CheaterB cells through exhaustive tests of their ability to
grow, develop, form spores and germinate. CheaterB did just as well in these
tests as its ancestor wild strain. Under laboratory conditions, at any rate,
CheaterB didn't seem to be paying a fitness cost for cheating.
The
study raises important questions about the tension between cooperation and
cheating. Why would breaking something that is presumably functional (by
knocking out a gene) confer an advantage in the first place? And if cheating
benefits the cheater and has no hidden cost, what holds cheating in check?
Cheating
is surprisingly easy
D.
discoideum spend
most of their lives as predatory single cells hunting bacteria through the leaf
litter and upper soil layers of forests in eastern North America. But when they
can't find bacteria and begin to starve, they gather to form fruiting bodies, a
thin stalk of cells with a ball of spores at the top, like a miniature Space
Needle. The amoebae that end up in the stalk die, giving up their lives to
benefit the amoebae that become spores.
Importantly
the cells that stream together to form the fruiting body can be clonal
(genetically identical) or have two (or more) genetic makeups. If each clone in
a two-clone fruiting body contributes half the cells to the spore body, both
clones gain from cooperating because each must sacrifice fewer cells to the
stalk.
But game
theory suggests the clones should sometimes evolve strategies that allow them
to gain the benefits of cooperation without paying the costs.
In 2008 Queller and Strassmann published a genome-wide screen of D. discoideum that
found roughly 180 cooperation genes, genes that might produce cheaters if they
mutated. The number of genes, and the number of different biological pathways
they affected, suggested it might be easy to evolve cheating and difficult to
control it fully.
At the time cheaters were believed to be held in check by
mechanisms that made non-cooperation costly. The first D. discoideum cheater
to be scrutinized, CheaterA, described in 2000, is not able to form fruiting
bodies on its own. This is a crippling disability that would prevent it from surviving
in the wild.
But the
screen from 2008 selected only clones able to produce clonal fruiting bodies,
thus passing a basic test of evolutionary fitness. These clones were what is
called facultative cheaters, cheating only under favorable conditions, and not
obligate cheaters, forced to cheat no matter what.
The
overall robustness of knockout mutant CheaterB deepens the mystery. "No
measurable laboratory trait revealed an Achilles heel," Strassmann says,
"but that doesn't mean there isn't one in natural environments. Otherwise,
why would a naturally occurring mutation that duplicated the knockout not take
over amobae populations?"
Source: Washington University in St.
Louis
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