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Telis, N.

Publications and source records attributed to Telis, N..

3 recordsLinked to original sources

Selection against archaic DNA in human regulatory regions

Traces of archaic hominin DNA persist in the human gene pool, but are systematically depleted around genes and other functionally important genomic regions. This suggests that many Neandertal and Denisovan alleles had harmful effects on hybrid fitness. We hypothesized that if some harmful effects were mediated by gene dysregulation in specific tissues, alleles previously flagged as archaic using a conditional random field (CRF) should be depleted from those tissues regulatory enhancers compared to "control" alleles matched for allele frequency and the strength of background selection. By this metric, both Neandertal and Denisovan variation appear depleted from enhancers, particularly enhancers that show pleiotropic activity across tissues. This depletion is driven by young archaic SNPs that the CRF confidently identifies as private to Neandertals or Denisovans; older variants that were likely present in both archaic species are not depleted from enhancers. We found that enhancer pleiotropy is not only a predictor of archaic SNP depletion, but also a predictor of intolerance to new mutations as measured by both phastCons scores and the frequency spectrum of African variation. In other respects, however, the landscape of selection against young archaic alleles appears qualitatively different from the landscape of ordinary purifying selection, suggesting that archaic alleles had a different distribution of fitness effects from ordinary new mutations. Most strikingly, fetal brain and muscle are the tissues most depleted of young archaic variation in their regulatory regions, but only brain enhancers appear commensurately intolerant to new mutations. In contrast, fetal muscle enhancers show no evidence of elevated purifying selection relative to other enhancers. This suggests that epistatic incompatibility between human and archaic alleles is needed to explain the degree of archaic variant depletion from fetal muscle enhancers, perhaps due to divergent selection for higher muscle mass in archaic hominins compared to humans.

evolutionary biology↗

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scientific communication and education↗

Pervasive adaptation in Plasmodium-interacting proteins in mammals

The protozoan genus Plasmodium causes malaria in dozens of mammal species, including humans, non-human primates, rodents, and bats. In humans, Plasmodium infections have caused hundreds of millions of documented deaths, imposing strong selection on certain populations and driving the emergence of several resistance alleles. Over the deep timescale of mammalian evolution, however, little is known about host adaptation to Plasmodium. In this work, we expand the collection of known Plasmodium-interacting-proteins (PIPs) in mammalian hosts from ~10 to 410, by manually curating thousands of scientific abstracts. We use comparative tests of adaptation to show that PIPs have experienced >3 times more positive selection than similar mammalian proteins, consistent with Plasmodium as a major and long-standing selective pressure. PIP adaptation is strongly linked to gene expression in the blood, liver, and lung, all of which are clinically relevant tissues in Plasmodium infection. Interestingly, we find that PIPs with immune functions are especially enriched for additional interactions with viruses or bacteria, which together drive a 3.7-fold excess of adaptation. These pleiotropic interactions with unrelated pathogens, along with pressure from other Plasmodium-like Apicomplexan parasites, may help explain the PIP adaptation we observe in all clades of the mammalian tree. As a case study, we also show that alpha-spectrin, the major membrane component of mammalian red blood cells, has experienced accelerated adaptation in domains known to interact specifically with Plasmodium proteins. Similar interactions with Plasmodium-like parasites appear to have driven substantial adaptation in hundreds of host proteins throughout mammalian evolution.

evolutionary biology↗