4.7 Article

The Divergence of Neandertal and Modern Human Y Chromosomes

Journal

AMERICAN JOURNAL OF HUMAN GENETICS
Volume 98, Issue 4, Pages 728-734

Publisher

CELL PRESS
DOI: 10.1016/j.ajhg.2016.02.023

Keywords

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Funding

  1. Stanford Center for Computational, Evolutionary, and Human Genomics (CEHG)
  2. National Science Foundation [1201234, DGE-1147470]
  3. National Library of Medicine [LM-007033]
  4. Max Planck Society
  5. Division Of Mathematical Sciences
  6. Direct For Mathematical & Physical Scien [1201234] Funding Source: National Science Foundation

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Sequencing the genomes of extinct hominids has reshaped our understanding of modern human origins. Here, we analyze similar to 120 kb of exome-captured Y-chromosome DNA from a Neandertal individual from El Sidron, Spain. We investigate its divergence from orthologous chimpanzee and modern human sequences and find strong support for a model that places the Neandertal lineage as an outgroup to modern human Y chromosomes-including A00, the highly divergent basal haplogroup. We estimate that the time to the most recent common ancestor (TMRCA) of Neandertal and modern human Y chromosomes is similar to 588 thousand years ago (kya) (95% confidence interval [CI]: 447-806 kya). This is similar to 2.1 (95% CI: 1.7-2.9) times longer than the TMRCA of A00 and other extant modern human Y-chromosome lineages. This estimate suggests that the Y-chromosome divergence mirrors the population divergence of Neandertals and modem human ancestors, and it refutes alternative scenarios of a relatively recent or super-archaic origin of Neandertal Y chromosomes. The fact that the Neandertal Y we describe has never been observed in modern humans suggests that the lineage is most likely extinct. We identify protein-coding differences between Neandertal and modem human Y chromosomes, including potentially damaging changes to PCDH11Y, TMSB4Y, USP9Y, and KDM5D. Three of these changes are missense mutations in genes that produce male-specific minor histocompatibility (H-Y) antigens. Antigens derived from KDM5D, for example, are thought to elicit a maternal immune response during gestation. It is possible that incompatibilities at one or more of these genes played a role in the reproductive isolation of the two groups.

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