Live from #Evol2017 – Sunday Highlights (and a smidge of Saturday too!)

A subset of the Molecular Ecologist team is attending this year’s Evolution meeting in Portland, Oregon. As part of our coverage of the meeting, we will recapping the highlights of each day here on the blog, and occasionally previewing upcoming presentations. You can find all of the TME contributors on Twitter using the sidebar on the right or compiled in a handy Twitter list here; follow along with all meeting news using the hashtag #Evol2017.

Team meeting at Teote


Stacy
As I’m taking care of the Sunday highlights, I am taking the liberty of inserting my Saturday highlights as well! In a separate post that will be written soon, I’ll regale the TME readers with the story of the stolen field gear …
Saturday
Carlos Spano et al. – Genomic divergence in sea anemones and it’s implications for species delimitation. They asked they dreaded question of what is a species for a sea anemone … there’s lots of plasticity and very simple morphologies, so what do you use to delimit species in these taxa? As my lab is making a foray into sea anemones soon with the addition of a post-doc (see more in my Sunday highlight), I thought this was an interesting foil to the current work on seaweed species delimitation we’ve been doing. It’s hard in these taxa, that’s certainly an understatement! I found it interesting that some synonymies were based on a single specimen without genomic tools! Another interesting point was raised in the questions in the frequency of asexual reproduction across the Anthothoe complex and what role that has in speciation. The work is still on-going, but what role does asexual reproduction play in divergence?
Sarah Jacobs and David Tank – species delimitation in the grey zone. Sarah stressed over and over again that we need (1) multiple lines of evidence, (2) multiple independent approaches and (3) integrative studies! They’ve been working on Castilleja and had to fall back on Sanger sequencing (which incidentally I found somewhat sad that older techniques are somewhat begrudgingly returned to even if they could be an appropriate tool!). While conducting power analyses, they found that one technique got the species right, the other technique they used, not so much. If you stumble across a Castilleja species, the first thing an expert will ask you is (1) where did you sample it, then (2) what was the ecological habitat and then (3) morphological characteristics. So are some of these conflated with one another?
Sunday
Will Ryan – while it might be shameless to highlight Will’s talk as he is joining my nascent lab in September, his stuff is just too cool! He presented work from his dissertation about an invasive sea anemone Diadumene lineata. It has temperature dependent fission. So, it undergoes both sexual and asexual reproduction. A bifurcation of a life cycle into these two reproductive modes must have some pretty awesome eco-evolutionary consequences! Along the east coast of the US, there’s a cline in fission rates that has an underlying genetic component!
Kathryn Turner – invasions in space and time using herbarium specimens. Herbaria truly are little nuggets of data … not just genomic, but also geographic location and a time capsule of info before an invasion … in other words, contemporary samples from sites that might have contributed to the invasion! Super cool to see what happens with the genomic work they’re doing with these samples! And, if you can help Kathryn out by looking for samples, get in touch (@KTInvasion).
Lua Lopez – herbarium data to track adaptation through time! In a time when herbaria and museum collections are losing funding, these studies are all the more important. They’re tracking adaptation in samples from 1820-2010! Funnily enough, the 1820 sample had tons of DNA, but it didn’t matter if you were an old sample or a new sample (i.e., 2010), the herbarium sample DNA is degraded and fragmented! Regardless, herbariums samples are “awesome for temporal studies!”
Jeremy
Alexandra Fraik — Characterizing potential adaptations of Tasmanian devil populations in the face of a transmissible cancer — Analysis of a sequence capture dataset from more than 3,000 Tasmanian devils, using both F[ST] outlier-type methods and genotype-environment associations to identify loci associated with incidence of the transmissible devil facial tumor. A particularly nice feature is that data’s included from before and after the arrival of the DFT in many populations, so there’s a basis for direct tests for selected loci.
Thomas Nelson — The timescales of selection in stickleback: Why rapid adaptation takes millions of years — Nice deep dive into variation in coalescent time across the stickleback genome, in the context of two transitions to freshwater from the same anadromous population. Variants that helped fuel adaptation to freshwater are older than the rest of the genome, and may have been maintained in the ancestral population by past moves into freshwater and back. (I swear, stickleback seem to make the jump to freshwater more often than I’ve crossed the US-Canada border.)
Rob
Paul Decena — Genome size evolution in neotropical salamanders.
I enjoyed this tidy talk by Paul Decena, who started with a simple enough idea: salamanders have huge genomes compared to other vertebrates, we know that cell size is correlated with genome size, so what do the genomes of the smallest salamanders look like? The answer might not surprise you. There is a positive relationship between salamander body size and genome size. However, those tiny genomes are still many times bigger than even the largest mammal genomes, so these miniaturized amphibians have distinct morphological features that allow for the minimum size of certain features that just can’t functionally get any smaller (like eyes!).
Jonathan Puritz — Expressed Exome Capture Sequencing (EecSeq): a method for cost-effective exome sequencing of non-model organisms
A packed room was eager to learn about EecSeq, an exome sequencing approach developed by Jonathan Puritz that skips the generation of transcriptomes/genomes in order to isolate exome data. The trick to this pipeline? A Jonathan said, “I can’t tell you the details because I don’t want someone to steal my idea. But if you come and find me after the talk and pinky swear not to tell, we can talk about it.”
Katie
Katie Wagner and Brian Smith — When are species delimitation methods misleading in the study of macroevolutionary patterns? and When are species delimitation methods necessary for studying macroevolutionary patterns?
These talks were presented back to back in the symposium titled “A debate of conceptual issues surrounding genetic-based species delimitation in the genomic era.” Although they were framed as opposing sides of a debate, the two talks were largely complementary (Katie Wagner prefaced her talk by telling the audience that debate was her least favorite class in high school). Both speakers agreed that species delimitation tools can help us understand genetic patterns on a landscape — including patterns above and below the species level.
Catalina Palacios — We’re one, but we’re not the same: Shallow evolutionary divergence between two andean hummingbirds
At the end of the day I stumbled into this talk by accident — and I was glad I did! Catalina and colleagues used an impressive suite of analyses to study two beautiful and charismatic hummingbird species from the Andes. Although the two species have notably different iridescent plumage coloration, Catalina found evidence of niche overlap and rampant mitochondrial haplotype sharing between them. Nuclear data, however, supported a distinct species split. She concluded that the two species had high levels of gene flow during the early stages of divergence.

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Live from #Evol2017 – Saturday Highlights

A subset of the Molecular Ecologist team is attending this year’s Evolution meeting in Portland, Oregon. As part of our coverage of the meeting, we will recapping the highlights of each day here on the blog, and occasionally previewing upcoming presentations. You can find all of the TME contributors on Twitter using the sidebar on the right or compiled in a handy Twitter list here; follow along with all meeting news using the hashtag #Evol2017.

Mt. Hood and the St. Johns Bridge in Portland, during decidedly cooler weather than conference attendees are currently experiencing. Flickr: Mark


To get things going, these were some of our favorite presentations from Saturday, June 24rd:
Jeremy
Sarah Fumagalli: Hidden Benefits Aid the Evolution of Altruism in Small Populations of Unrelated Individuals
— Builds a model of altruistic behavior with stochastic selection and explicit tracking of trait-environment covariation, and recovers a bunch of classic evolution-of-altruism results from first principles. What’s really cool, though, is that there’s a possibility that increased altruism can evolve by chance in a small population of unrelated individuals, and kickstart selection for more altruism.
Melissa Wilson Sayres: Teaching undergraduate life sciences majors
— Surveyed biology faculty to zero in on what “core competencies” of bioinformatics should be part of a standard life science curriculum. Notably, lots of folks ranked statistics as important, even though you’d think that’s a basic component of every bio program already. And lots of respondents ranked command-line skills as important. A sample of syllabi found a lot of variation in what competencies are actually covered in bioinformatics courses, though.
Rob
Jeet Sukumaran: Species Delimitation under the Multispecies Coalescent: Conflating Populations with Species in the Grey Zone
— I think that if you begin a talk by reflecting on a recent paper of yours, you are (brazenly?) making a big assumption that the paper has been read by a majority of your audience. In this case, that assumption was completely justified as a full room of other scientists nodded their heads as we were reminded that multispecies coalescent theory is actually concerned with population structure, not whatever species concept you overlay on top of it. A simple message that resonated, just like the corresponding PNAS paper from late last year.
Greg Haenel: Variation of mitochondrial function in hybrid Tree lizards: assessing the role of differential gene expression
— Cases of mitochondrial introgression across a wide variety of systems continue to pop up in session after session, but nailing down the mechanisms that drive this introgression is a trickier problem. Greg Haenel offered a neat system to investigate further, tree lizards that have hybridized across a stark temperature gradient. The expression analyses show differences associated with those hybrid mitochondria, but the work to tease out how these differences potentially related to interacting mitochondrial and nuclear DNA is just taking off.
Ethan
Rebekah Rogers: Excess of genomic defects in a woolly mammoth on Wrangel island
— Using the high-quality genomes from Wrangel Island and mainland Siberia published by Eleftheria Palkopoulou et al. in 2015, Rogers explored the genomic defects present in an individual from the last surviving mammoth population. In her standing-room-only talk, Rogers kept one foot firmly rooted in population genetic theory (“to tell you what is possible”) while speculating on the biology of some very mutation-burdened mammoths (shiny pelts!).
Harry Greene: Teaching natural history in the Anthropocene: some rules of engagement
— Given as part of an American Society of Naturalists symposium (“Natural history as the inspiration for scientific inquiry: Stories and tools for teaching”), Greene’s talk focused on on a question I spend a lot of time thinking about: what concepts of “wilderness” mean to a biologist, especially in our current human-dominated epoch. In Greene’s eyes, this has less to do with traditional notions of what qualifies “pristine” or “disturbed” and more with how intact ecological and evolutionary processes are. I like this formulation because it highlights the role of humans as participants (versus spectators) in evolution, but still provides a moral compass for addressing conservation questions.

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When less might be more: The evolution of reduced genomes


The advent of affordable genome sequencing has provided us with a wealth of data. Researchers have sequenced everything from Escherichia coli (4.6 Mbp genome size), to sea urchins (810 Mbp), chimpanzees (3.3 Gbp), and humans (3.2 Gbp). Then there are the massive genomes, which have been identified, including that of the rare Japanese flower (Paris japonica) with a genome of 149 Gbp. But, what does that mean? Maybe it’s more interesting to switch our focus from the large and in charge genomes to those of the small free living prokaryotes who have taken the opposite route.
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Molecular Ecologists at #Evol2017 —  see you in Portland!

The Portland skyline and Mt. Hood, as seen from the Portland Japanese Garden. (Flickr: Alan)


Evolution 2017 — the joint annual meeting of the American Society of Naturalists, the Society of Systematic Biologists, and the Society for the Study of Evolution — is already underway in Portland, Oregon, and it’s looking like a terrific week of science already. The program kicked off today with a symposium in honor of Joe Felsenstein, and gets fully underway tomorrow with a day of workshops capped by the traditional public outreach lecture, which will be given by Ann Reid, the Executive Director of the National Center for Science Education. Regular presentation sessions begin bright and early Saturday morning, and carry on through Tuesday.
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On hyRAD-X, another option for museum genomics

Last year, I profiled Suchan et al.’s “hyRAD” method for reduced-representation genome sequencing of degraded sources of DNA using RAD probes. While it’s too early to say whether hyRAD will be widely used by molecular ecologists looking to integrate historic samples into their work–in my own research, I found it effective, but not efficient–it remains a promising step forward for population genomics with a temporal dimension.
Now, the team behind hyRAD have published a major update to their protocol (“hyRAD-X”), replacing fragments from a RAD digest with messenger RNA as the basis for the probes in target capture. This, the authors argue, improves on the original method in several ways. First, as the reference used in bioinformatics steps is an assembled transcriptome from RNAseq of one high-quality tissue sample, both loci definition and SNP calling accuracy are improved. Second, the RNA probes in the method increase hybridization stringency — an important improvement for low-content DNA samples. (Arguably the main reason to apply hyRAD-X in the first place!)
So which method should you use? On the one hand, hyRAD-X’s advantages appear numerous, and address many of the problems inherent to the original protocol. Targeting the exome reduces the likelihood of capturing paralogous loci, as repetitive genomic regions are more frequently found in noncoding DNA. RNA probes are more thermodynamically stable, and eliminate the risk of contamination and chimera formation. Nor is hyRAD-X dramatically more complicated at the lab bench, deviating from hyRAD only in its probe generation step, where biotinylated RNA is synthesized from cDNA itself synthesized from a total RNA extract of a single high-quality sample. By integrating biotin-UTP during the in-vitro transcription stage of this process, the method also avoids the substantial probe material loss probably with the nick-labeling mechanisms proposed in Suchan et al. 2012. And in a comparison of the performance of both methods on an identical timeseries of conifer subfossils (spanning 7200 – 5800 years bp), Schmid et al. report significantly more SNPs from hyRAD-X than hyRAD with a de novo reference, and significantly greater mean read depth per site.

**Figure 2** from Schmid et al. 2017, diagramming the hyRAD-X method.


On the other hand, these benefits are not abundantly clear from the author’s published results. Schmid et al. report no differences in percentage of missing data, overall mean read depth, or chimera production. Concerningly, they do report 2-8 times higher PCR duplicates in hyRAD-X compared to hyRAD alignments. (I found PCR duplicates to a be pervasive feature of my own hyRAD captures, and are an important consideration when deciding sequencing effort.) And when comparing hyRAD-X and hyRAD data aligned to an identical transcriptome, the original hyRAD protocol resulted in a higher percentage of mapped reads and a greater SNPs, suggesting its primary limitations may have been related to the inherent problems with de novo reference genomes. Finally, putatively neutral loci may be preferable to exome data in some cases where sites under selection violate the assumptions of population genetic models, or bias phylogenetic inference.
However these issues come out in the wash, I think the decision to apply hyRAD, hyRAD-X, or another probe-based method for reduced representation sequencing historic samples is more likely to be based on your project’s goals and your lab’s contingencies than any clear advantages of a particular protocol. But while there may not yet be a silver bullet for population genomics with degraded DNA, it’s undoubtedly an exciting time to be working in the field, and hyRAD-X represents a creative solution to its many challenges.

References

Schmid, S., Genevest, R., Gobet, E., Suchan, T., Sperisen, C., Tinner, W., Alvarez, N. 2017. HyRAD-X, a versatile method combining exome capture and RAD sequencing to extract genomic information from ancient DNA. DOI: 10.1111/2041-210X.12785
Suchan, T., Pitteloud, C., Gerasimova, N.S., Kostikova, A., Schmid, S., Arrigo, N., Pajkovic, M., Ronikier, M., Alvarez, N. 2016. Hybridization Capture Using RAD Probes (hyRAD), a New Tool for Performing Genomic Analyses on Collection Specimens. PLoS One. DOI: 10.1371/journal.pone.0151651

Posted in genomics, methods, natural history, next generation sequencing, phylogenetics, phylogeography, population genetics, RNAseq, selection, transcriptomics | Tagged , , , | Leave a comment

Shared patterns of genomic diversity across populations of distantly related taxa

Genomic diversity is shaped by the complex interplay between the effects of genetic drift and natural selection among populations. Several of these effects, especially those of linked selection at neutral sites, adaptive introgression, and barriers to migration (often called “genomic islands”) have been discussed on our blog before, all of which compare diversity within species, or among closely related species.
In a recent study, Vijay et al. 2017 propose a “macro-level comparative approach”, comparing genomic diversity across taxa, under the hypothesis that shared patterns of diversity across distantly related taxa are characteristic of shared demographic history (here characterized by the effective population size, Ne, and variants of it) across syntenic regions.

Genome-wide patterns of summary statistics measured across whole genomes of three species of birds – Darwin’s finches, flycatchers, and American crows. Figure from Fig. 2 of Vijay et al. 2017 (http://dx.doi.org/10.1111/mec.14195)


Vijay et al. (2017) analyzed shared polymorphisms across publicly available genomes of three disparate clades of Darwin’s finches, flycatchers, and American crows, with ~50 million years of evolution between them. Thereon, summary statistics including population recombination rates, nucleotide diversities, divergences, and Fst were computed in 50 Kb windows. Similarities within and among clades were then computed using Pearson correlations. Results indicated several interesting findings: (1) strong correlations within clades among all summary statistics computed, as expected – for example, dxy is expected to be negatively correlated with Fst under the effects of linked selection (2) high levels of between clade correlations, particularly in dxy estimates, and recapitulation of the negative correlation between dxy and Fst when comparing across clades, and (3) significant correlation across estimates of summary statistics concentrated around sub-telomeric regions, rather than in peri-centromeric regions (which also had reduced diversity, elevated differentiation), indicative of the influence of chromosomal recombination rates in mitigating the effects of linked selection/differential introgression.
These results suggest that syntenic genomic regions evolving putatively due to linked natural selection experience similar effects across millions of years of evolution.

The degree of correlation among clades was remarkable considering divergence times of several million generations, gaps in syntenic alignments and the statistical error associated with population genetic estimates from moderate samples sizes. With recombination rate being the key mediator of linked selection, an explanation of genomic parallelism in Ne through linked selection requires conserved recombination landscapes among the clades under investigation.

 
Reference:
Genome-wide patterns of variation in genetic diversity are shared among populations, species and higher order taxa, Nagarjun Vijay, Matthias Weissensteiner, Reto Burri, Takeshi Kawakami, Hans Ellegren and Jochen B. W. Wolf, Molecular Ecology, DOI: 10.1111/mec.14195
 

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Friday action item: It's time to go local

Screencap of weather.com, which is not having this. (Twitter: Eric Holthaus)


On Fridays while the current administration is in office we’re posting small, concrete things you can do to help make things better. Got a suggestion for an Action Item? E-mail us!
This Thursday was not a good day for the world, or for the standing of the United States in the world:

President Trump has announced that the U.S. will be withdrawing from the Paris accord — the historic global agreement reached by 195 countries in 2015 to set targets for reducing greenhouse gas emissions and limiting the rise in average global temperatures.

This administration has done plenty of awful things, but this move is a kind of nexus of everything that came before — disdainful of hard-won international cooperation, short-sighted even from a purely business-oriented perspective, deliberately ignorant of scientific consensus, and likely to visit its greatest harms on the poorest people on the planet. The Paris Agreement was, to some extent, a symbol — the Trump Administration was already merrily gutting the infrastructure of environmental protection before today, and formal withdrawal could take almost four years to complete — but the announcement makes crystal clear that the U.S. Federal Government is abdicating any role it could have in facing the global threat that defines our generation.
Even without Federal leadership, though, we have options at the local level. Because today’s announcement was hardly a surprise, some of them are already set to go. The states of Washington, California, and New York, which together account for about a fifth of the U.S. population and GDP have announced an alliance to coordinate carbon emissions reductions without D.C., with the explicit goal of meeting the Paris commitments. The new organization is billed as an extension of the Under2 Coalition, an international coalition of cities, states, and other “sub-national” governments that signed a memo of understanding for joint action on carbon emissions starting in 2015. A number of other states’ governors pledged independent action in anticipation of Thursday’s announcement — so one thing you can do today is call up your governor’s office and your state representatives to ask, why isn’t my state in the U.S. Climate Alliance already?

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Nancy Moran awarded the 2017 Molecular Ecology Prize

Nancy Moran’s most cited paper used metagenomics to identify a possible cause of honeybee colony collapse disorder. (Flickr: Rachel Bonoan)


The 2017 Molecular Ecology Prize will go to Professor Nancy Moran of the University of Texas at Austin. The Prize is awarded by the Editorial Board of Molecular Ecology to recognize “an outstanding scientist who has made significant contributions to Molecular Ecology,” as selected by an independent award committee. Professor Moran’s nomination statement particularly highlights her extensive work on symbiosis and microbial community genetics:

Nancy Moran, from her Google Scholar citations page.

The 2017 Molecular Ecology Prize has been awarded to Professor Nancy Moran for her pioneering studies of symbiosis and bacterial genome evolution. Her discoveries provide a clear link between bacterial lifestyle and population size with rates of evolution and genome degradation. Her work has also provided some of the most convincing demonstrations of the molecular basis for ecologically important traits, including defense, nutrition, and thermotolerance, inclucing remarkable examples of convergence mediated via symbiosis. Professor Moran’s more recent work on the honeybee system is now setting the standard for molecular studies of complex symbiotic gut communities.

Previous Molecular Ecology Prize recipients include Godfrey Hewitt, John Avise, Pierre Taberlet, Harry Smith, Terry Burke, Josephine Pemberton, Deborah Charlesworth, Craig Moritz, Laurent Excoffier, Johanna Schmitt, Fred Allendorf and Louis Bernatchez.

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Friday action item: An awful budget, now with detail


On Fridays while the current administration is in office we’re posting small, concrete things you can do to help make things better. Got a suggestion for an Action Item? E-mail us!
There’s a detailed Federal budget proposal out this week, covering the Trump administration’s plans for the 2018 fiscal year. Have you called Congress about it? You should.
Detailed breakdowns have identified cruel cuts to the social safety net and a multi-trillion-dollar arithmetic error that make excellent reasons to oppose the plan all on their own. But there’s also piles of bad news for science:

We’ve also, for the first time, got a concrete proposal for the National Science Foundation’s budget — more than 11% lower than what it had in 2016 — to the lowest it’s been, in inflation un-adjusted dollars, since 2008. The spending plan NSF has prepared with that number in mind would reduce funding for graduate research fellowships, EPSCoR support for institutions in states that otherwise receive less NSF funding, and the research at undergraduate institutions (RUI) program, among others.
As we saw with the Trump proposal for continuing funding in 2017, this will almost certainly not pass Congress in its current state; but Congress can use every bit of encouragement we give it. Call!

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Molecular adaptation in a deep-sea alien…*ahem* amphipod

Space: the final frontier…or is it? I was inspired Jeremy’s post yesterday to talk about that deep dark abyss that takes up the vast majority of our mostly blue planet. For the record, I’m in agreement with the assessments for the marine (micro)biologists. After perusing images of the critters down there, you might wonder if it’s not more interesting (or at least equally interesting) to dive deep under the ocean to see what might be the closest to aliens we can currently get (discussed recently here). One glimpse of a goblin shark (maybe kinda scary for some kids) or anglerfish, should convince you.
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