What They Did
The researchers examined the possibility of gene flow
between different subspecies of monkeyflower, Mimulus aurantiacus. One
subspecies, parviflorus, is only found on islands off the coast of California.
Another subspecies, longiflorus, grows both on the islands and the mainland.
The researchers compared DNA from both island and mainland populations of longiflorus,
parviflorus, and aridus the sister subspecies of parviflorus.
Examining the whole genome at once shows that the two
populations of longiflorus are most closely related to each other and
that parviflorus is most closely related to aridus. Comparing
only parts of the genome at a time, however, reveals where gene flow may have
occurred. In some sections of the genome, the island population of longiflorus
is more similar to parviflorus than to the mainland longiflorus population.
This suggests that some gene flow occurred between the two subspecies on the
island. In other parts of the genome, parviflora is more similar to both
island and mainland longiflorus than it is to aridus, suggesting
that there was some gene flow between the ancestor of parviflora and the
ancestor of longiflorus, before the mainland and island populations diverged.
Looking more closely at one chromosome, they found a section
where many alleles matched in parviflora and in island longiflorus,
but not in aridus, the sister subspecies of parviflorus. They did
not, however, see many matches between parviflora and island longiflorus
that differed from mainland longiflorus. This suggests that gene
flow caused adaptive changes in the parviflora genome but not the other
way around.
Further Exploration
Back when I was a biology lab TA, I remember learning about
some other monkeyflower that underwent “instant speciation” when there was a
genome replication event. It’s not all that rare for the chromosomes to fail to
separate during meiosis in plants, so that one gamete has a double set of
chromosomes and one has none. When, for example, a diploid egg is fertilized by
a haploid sperm, the resulting offspring is triploid, with three sets of
chromosomes. Plants can often survive fine with extra sets of chromosomes, but when
they undergo meiosis, the chromosome numbers might not be typical for their species,
which can lead to reproductive isolation and speciation.
Monkeyflowers are often used in research about evolution and
speciation because there’s a lot of phenotypic variation but still enough
genetic similarity to cross taxa pretty easily. The plants also grow quickly
and produce a lot of seeds (see https://monkeyflower.eeb.uconn.edu/a-new-genetic-model-system-monkeyflowers/).
The different flower shapes and colors attract different pollinators, and the
plants grow in all sorts of habitats and can be herbs or shrubs (see https://phytozome-next.jgi.doe.gov/info/Mguttatus_v2_0).
Since monkeyflowers of different species can often
crossbreed, it’s not surprising that the subspecies mentioned in today’s
journal article also show evidence of gene flow. The fact that (at least on one
chromosome), alleles from longiflorus became fixed in parviflorus suggests
that those alleles were useful enough to be selected for. It would be
interesting to compare the areas of high gene flow on the other chromosomes,
but that’s a rabbit hole for another day!
https://commons.wikimedia.org/wiki/File:Mimulus_aurantiacus_(148194242).jpg
Hi Kimberly! Thank you for taking the time to summarize our research in your blog post! I really appreciate your excitement and passion for science!
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