[Taxacom] Congruence of gene trees
Michael Heads
michael.heads at yahoo.com
Fri Aug 14 19:10:52 CDT 2009
Hi Richard,
Ancestors may be polymorphic (cf. Heads, M. 1985. On the nature of ancestors. Systematic Zoology 34: 205-215.). If lineage sorting in the ancestor is incomplete there is no 'clean slate' (pure monomorphism) in the ancestor before a new round of differentiation begins. The old polymorphism may be inherited and may have a spatial distribution quite different from the new break. The end result of incomplete lineage sorting in the ancestor - the incongruence - is similar to that of hybridism, but ILS occurred before the differentiation of the new subclades, hybridism after. ILS explains incongruence in any character tree, molecular or morphological. See also: Heads, M. 2009. Darwin’s changing ideas on evolution: from centres of origin and teleology to vicariance and incomplete lineage sorting. Journal of Biogeography 36: 1018-1026.
Michael Heads
Wellington, New Zealand.
My papers on biogeography are at: http://tiny.cc/RiUE0
--- On Sat, 8/15/09, Richard Zander <Richard.Zander at mobot.org> wrote:
From: Richard Zander <Richard.Zander at mobot.org>
Subject: [Taxacom] Congruence of gene trees
To: "Jason Mate" <jfmate at hotmail.com>, "Taxacom" <taxacom at mailman.nhm.ku.edu>
Date: Saturday, August 15, 2009, 11:18 AM
Disparate congruence of results of different genes (sequences) between
the sequences has long been known. Many gene trees have apparently
different histories (differential lineage sorting). Some trios (like
man, chimp, gorilla) have most genes supporting one tree (man, chimp
terminal) and about equal but fewer numbers of genes supporting two
alternative full resolutions (man, gorilla terminal) and (chimp, gorilla
terminal). All or many gene trees may be well supported, which supports
their discrepant histories. But then the distributions become governed
by small sample statistics (requiring assumed distributions) in most
cases but a few.
The explanation is fairly well-known, but the functional basis as it
affects statistics is not understood at least by me. Okay, the null is
not that all three trees are equal in probability, but instead the null
is that only one tree is possible given shared ancestry. The null is
that some process forces some gene trees into wrong configurations, and
this process is equiprobable in the two alternative wrong
configurations. We then assume that the two least common configurations
are probably the wrong ones. I think that works okay.
So what is the process that makes some trees wrong? Why is it
equiprobable for all possible trees? Is it "oh, I'm late homogenizing in
the population" and two polymorphisms are fixed during speciation
instead of one? Or some selection might be involved such that
equiprobable wrong configurations are not to be expected?
Someone enlighten us?
*****************************
Richard H. Zander
Voice: 314-577-0276
Missouri Botanical Garden
PO Box 299
St. Louis, MO 63166-0299 USA
richard.zander at mobot.org
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*****************************
-----Original Message-----
From: taxacom-bounces at mailman.nhm.ku.edu
[mailto:taxacom-bounces at mailman.nhm.ku.edu] On Behalf Of Jason Mate
Sent: Friday, August 14, 2009 5:31 PM
To: Taxacom
Subject: Re: [Taxacom] Molecules vs Morphology
I am somewhat confused by this. If evolution does not act on every
aspect of the organism equally all the time and lineages are independent
why would you expect congruence throughout? You can have local
incongruence between any two particular datasets simply out of chance or
because the gene-tree of one molecular dataset is different from the
other due to the speciation process. It is the average of many datasets
that you want as your best-available-hypothesis.
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