Paper detail

Modern alleles in archaic human Y chromosomes support origin of modern human paternal lineages in Asia rather than Africa

Recent studies have shown that hybridization between modern and archaic humans was commonplace in the history of our species. After admixture, some individuals with admixed autosomes carried the modern Homo Sapiens uniparental DNAs, while the rest carried the archaic versions. Coevolution of admixed autosomes and uniparental DNAs is expected to cause some of the sites in modern uniparental DNAs to revert back to archaic alleles, while the opposite process would occur (from archaic to modern) in some of the sites in archaic uniparental DNAs. This type of coevolution is one of the elements that differentiate the two different models of the Y phylogenetic tree of modern humans, rooting it either in Africa or East Asia. The expected reversion to archaic alleles is assumed to occur and is easily traceable in the Asia model, but is absent in the Africa model due to its infinite site assumption, which also precludes the independent or convergent mutation to modern alleles in archaic uniparental DNAs since mutations are assumed to occur randomly across a neutral genome, and convergent evolution is assumed not to occur. Here, we examined newly published high coverage Y chromosome sequencing data of two Denisovan and two Neanderthal samples to determine whether they carry modern-Homo Sapiens alleles in sites where they are not supposed to according to the Africa model. The results showed that a significant fraction of the sites that, according to the Asia model, should differentiate the original modern Y from the original archaic Y carried modern alleles in the archaic Y samples here. Some of these modern alleles were shared among all archaic humans while others could differentiate Denisovans from Neanderthals. The observation is best accounted for by coevolution of archaic Y and admixed modern autosomes, and hence supports the Asia model, since it takes such coevolution into account.

preprint2020arXivOpen access

Signal facts

What is known right now

Open access2 authors1 topic

Next steps

Decide what to do with this paper

Use like or dislike for the fast social read. The more specific scholarly feedback stays available below when needed.

Log in to curate

Reading frame

Keep the important context close to the paper

Keep the important signals around this paper in one place: votes, save state, collection context, reviews and the metadata you need before deciding what to do next.

Institutions

Add specific reaction

Move through the context

Research map

Open full explorer

Move through nearby people, institutions, topics and adjacent work without leaving the paper page.

Building this map preview

BZPEER is loading the nearby papers, people, topics and institutions for this page.

Structured reviews

0 review(s)

ContributeLeave structured feedbackUse the review template when you have a concrete strength, concern or method question.Open review form

No structured reviews yet. High-signal critique starts here.

Work discussion

0 comment(s)

DiscussAdd a high-signal commentKeep quick notes, caveats and replication pointers separate from formal reviews.Open comment form

No discussion yet. The first strong comment sets the tone.