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Since 2005, evidence for substantial admixture of Neanderthal DNA in modern populations is accumulating.[2][3][4]
The divergence time between the Neanderthal and modern human lineages is estimated at between 750,000 and 400,000 years ago.
The recent time is suggested by Endicott et al. (2010)[5]
and Rieux et al. (2014).[6]
A significantly deeper time of parallelism, combined with repeated early admixture events, was calculated by Rogers et al. (2017).[7]
In 2008 Richard E. Green et al. from Max Planck Institute for Evolutionary Anthropology in Leipzig, Germany, published the full sequence of Neanderthal mitochondrial DNA (mtDNA) and suggested "Neanderthals had a long-term effective population size smaller than that of modern humans."[9]
In the same publication, it was disclosed by Svante Pääbo that in the previous work at the Max Planck Institute, "Contamination was indeed an issue," and they eventually realised that 11% of their sample was modern human DNA.[10][11] Since then, more of the preparation work has been done in clean areas and 4-base pair 'tags' have been added to the DNA as soon as it is extracted so the Neanderthal DNA can be identified.
Among the genes shown to differ between present-day humans and Neanderthals were RPTN, SPAG17, CAN15, TTF1, and PCD16.[13]
A visualisation map of the reference modern-human containing the genome regions with high degree of similarity or with novelty according to a Neanderthal of 50 ka[12] has been built by Pratas et al.[14]
Researchers addressed the question of possible interbreeding between Neanderthals and anatomically modern humans (AMH) from the early archaeogenetic studies of the 1990s.
As late as 2006, no evidence for interbreeding was found.[15] As late as 2009, analysis of about one third of the full genome of the Altai individual showed "no sign of admixture". The variant of microcephalin common outside Africa, suggested[16] to be of Neanderthal origin and responsible for rapid brain growth in humans, was not found in Neanderthals; nor was a very old MAPT variant found primarily in Europeans.[10] However, more recent studies have concluded that gene flow between Neanderthals and AMH occurred multiple times over thousands of years.[17]
Positive evidence for admixture was first published in May 2010.[13] Neanderthal-inherited genetic material is found in all non- Sub Saharan African populations and was initially reported to comprise 1 to 4 percent of the genome.[13] This fraction was refined to 1.5 to 2.1 percent.[12] Further analyses have found that Neanderthal gene flow is even detectable in African populations, suggesting that some variants obtained from Neanderthals posed a survival advantage.[17]
Approximately 20 percent of Neanderthal DNA survives in modern humans; however, a single human has an average of around 2% Neanderthal DNA overall with some countries and backgrounds having a maximum of 3% per human.[18]
Modern human genes involved in making keratin, a protein constituent of skin, hair, and nails, contain high levels of introgression. For example, the genes of approximately 66% of East Asians contain a POUF23L variant introgressed from Neanderthals,[clarification needed] while 70% of Europeans possess an introgressed allele of BNC2. Neanderthal variants affect the risk of developing several diseases, including lupus, biliary cirrhosis, Crohn's disease, type 2 diabetes, and SARS-CoV-2.[18][19][20] The Val92Met variant of the MC1R gene, which has not been found in Neanderthal genomes but is putatively Neanderthal, and may be weakly associated with red hair and UV radiation sensitivity,[21] is found at a frequency of 5% in Europeans, 70% in Taiwanese and 30% in other East Asian populations.[22]
While interbreeding is the most parsimonious interpretation of these genetic findings, the 2010 research of five present-day humans from different parts of the world does not rule out an alternative scenario, in which the source population of several non-African modern humans was more closely related than other Africans to Neanderthals because of ancient genetic divisions within early Hominoids.[13][23]
Research since 2010 refined the picture of interbreeding between Neanderthals, Denisovans, and anatomically modern humans.
Interbreeding appears asymmetrically among the ancestors of modern-day humans, and this may explain differing frequencies of Neanderthal-specific DNA in the genomes of modern humans. Vernot and Akey (2015) concluded the greater quantity of Neanderthal-specific DNA in the genomes of individuals of East Asian descent (compared with those of European descent) cannot be explained by differences in selection.[25]
They suggest "two additional demographic models, involving either a second pulse of Neanderthal gene flow into the ancestors of East Asians or a dilution of Neanderthal lineages in Europeans by admixture with an unknown ancestral population" are parsimonious with their data.[25]
Kim and Lohmueller (2015) reached similar conclusions:
" According to some researchers, the greater proportion of Neanderthal ancestry in East Asians than in Europeans or West Asians is due to purifying selection is less effective at removing the so-called 'weakly-deleterious' Neanderthal alleles from East Asian populations. Computer simulations of a broad range of models of selection and demography indicate this hypothesis cannot account for the higher proportion of Neanderthal ancestry in East Asians than in Europeans. Instead, complex demographic scenarios, likely involving multiple pulses of Neanderthal admixture, are required to explain the data."[26]
Khrameeva et al. (2014), a German-Russian-Chinese collaboration,
compiled an elementary Neanderthal genome based on the Altai individual and three Vindjia individuals.
This was compared to a consensus chimpanzee genome as the out-group
and to the genome of eleven modern populations (three African, three East Asian, three European).
Beyond confirming a greater similarity to the Neanderthal genome in several non-Africans than in Africans, the study also found
a difference in the distribution of Neanderthal-derived sites between Europeans and East Asians, suggesting recent evolutionary pressures. Asian populations showed clustering in
functional groups related to immune and haematopoietic pathways,
while Europeans showed clustering in functional groups related to the lipid catabolic process.[27]
Kuhlwilm et al. (2016) presented evidence for AMH admixture to Neanderthals at roughly 100,000 years ago.[28]
At minimum, research indicates three episodes of interbreeding. The first occurred with some modern humans. The second occurred after the ancestral Melanesians branched off; these people seem to have bred with Denisovans. The third involved Neanderthals and the ancestors of East Asians only.[29][30][31]
2016 research indicates some Neanderthal males might not have viable male offspring with some AMH females.
This could explain the reason why no modern man has a Neanderthal Y chromosome.[32]
In October 2023, scientists reported that an anatomically-modern-human-to-Neanderthal admixture event occurred roughly 250,000 years ago, and also noted that roughly 6% of the Altai Neanderthal genome was inherited from anatomically modern humans. [33]
In December 2023, scientists reported that genes inherited by modern humans from Neanderthals and Denisovans may biologically influence the daily routine of modern humans, including the ability for some humans to wake earlier than others.[34] Similar to Europeans, modern Indians derive around 1-2% genetic make-up from ancient hominins, Neanderthals and Denisovans, however, Indians carry a much larger variety of these ancient genes compared with other populations.[35][36] It is unclear what, if any, advantage these genes may have provided.
Epigenetics
Complete DNA methylation maps for Neanderthal and Denisovan individuals were reconstructed in 2014.[37]
Differential activity of HOX cluster genes lie behind many of the anatomical differences between Neanderthals and modern humans, especially in regards to limb morphology. In general, Neanderthals possessed shorter limbs with curved bones.[37][38]
^Ovchinnikov, Igor V.; Götherström, Anders; Romanova, Galina P.; Kharitonov, Vitaliy M.; Lidén, Kerstin; Goodwin, William (2000). "Molecular analysis of Neanderthal DNA from the northern Caucasus". Nature. 404 (6777): 490–93. Bibcode:2000Natur.404..490O. doi:10.1038/35006625. PMID10761915. S2CID3101375.
^Endicott, Phillip; Ho, Simon Y.W.; Stringer, Chris (July 2010). "Using genetic evidence to evaluate four palaeoanthropological hypotheses for the timing of Neanderthal and modern human origins". Journal of Human Evolution. 59 (1): 87–95. doi:10.1016/j.jhevol.2010.04.005. PMID20510437. S2CID223433.
^Rogers, Alan R.; Bohlender, Ryan J.; Huff, Chad D. (12 September 2017). "Early history of Neanderthals and Denisovans". Proceedings of the National Academy of Sciences. 114 (37): 9859–9863. Bibcode:2017PNAS..114.9859R. doi:10.1073/pnas.1706426114. PMC5604018. PMID28784789.;
see also:
Jordana Cepelewicz, Genetics Spills Secrets From Neanderthals' Lost History, Quanta Magazine, 18 September 2017.
"The dating of that schism between the Neanderthals and the Denisovans is surprising because previous research pegged it as much more recent: a 2016 study, for instance, set it at only 450,000 years ago. An earlier separation means we should expect to find many more fossils of both eventually. It also changes the interpretation of some fossils. Take the large-brained hominid bones belonging to a species called Homo heidelbergensis, which lived in Europe and Asia around 600,000 years ago. Paleoanthropologists disagreed about how they relate to other human groups, some positing they were ancestors of both modern humans and Neanderthals, others claim they were a non-ancestral species replaced by the Neanderthals in their spread across Europe."
^ abcdGreen, Richard E.; Krause, Johannes; Briggs, Adrian W.; Maricic, Tomislav; Stenzel, Udo; Kircher, Martin; Patterson, Nick; Li, Heng; Zhai, Weiwei; Fritz, Markus Hsi-Yang; Hansen, Nancy F.; Durand, Eric Y.; Malaspinas, Anna-Sapfo; Jensen, Jeffrey D.; Marques-Bonet, Tomas; Alkan, Can; Prüfer, Kay; Meyer, Matthias; Burbano, Hernán A.; Good, Jeffrey M.; Schultz, Rigo; Aximu-Petri, Ayinuer; Butthof, Anne; Höber, Barbara; Höffner, Barbara; Siegemund, Madlen; Weihmann, Antje; Nusbaum, Chad; Lander, Eric S.; Russ, Carsten (2010). "A Draft Sequence of the Neanderthal Genome". Science. 328 (5979): 710–22. Bibcode:2010Sci...328..710G. doi:10.1126/science.1188021. PMC5100745. PMID20448178.
^Pratas, Diogo; Hosseini, Morteza; Silva, Raquel M.; Pinho, Armando J.; Ferreira, Paulo J. S. G. (2017). "Visualization of Distinct DNA Regions of the Modern Human Relatively to a Neanderthal Genome". Pattern Recognition and Image Analysis. Lecture Notes in Computer Science. Vol. 10255. pp. 235–242. doi:10.1007/978-3-319-58838-4_26. ISBN978-3-319-58837-7.
^Evans PD, Mekel-Bobrov N, Vallender EJ, Hudson RR, Lahn BT (November 2006). "Evidence that the adaptive allele of the brain size gene microcephalin introgressed into Homo sapiens from an archaic Homo lineage". Proceedings of the National Academy of Sciences of the United States of America. 103 (48): 18178–83.
^Lowery, Robert K.; Uribe, Gabriel; Jimenez, Eric B.; Weiss, Mark A.; Herrera, Kristian J.; Regueiro, Maria; Herrera, Rene J. (November 2013). "Neanderthal and Denisova genetic affinities with contemporary humans: Introgression versus common ancestral polymorphisms". Gene. 530 (1): 83–94. doi:10.1016/j.gene.2013.06.005. PMID23872234.
^
"Specifically, genes in the LCP [lipid catabolic process] term had the greatest excess of NLS in populations of European descent, with an average NLS frequency of 20.8±2.6% versus 5.9±0.08% genome wide (two-sided t-test, P<0.0001, n=379 Europeans and n=246 Africans). Further, among examined out-of-Africa human populations, the excess of NLS [Neanderthal-like genomic sites] in LCP genes was only observed in individuals of European descent: the average NLS frequency in Asians is 6.7±0.7% in LCP genes versus 6.2±0.06% genome wide."
Khrameeva, Ekaterina E.; Bozek, Katarzyna; He, Liu; Yan, Zheng; Jiang, Xi; Wei, Yuning; Tang, Kun; Gelfand, Mikhail S.; Prufer, Kay; Kelso, Janet; Paabo, Svante; Giavalisco, Patrick; Lachmann, Michael; Khaitovich, Philipp (2014). "Neanderthal ancestry drives evolution of lipid catabolism in contemporary Europeans". Nature Communications. 5: 3584. Bibcode:2014NatCo...5.3584K. doi:10.1038/ncomms4584. PMC3988804. PMID24690587..