
Human evolution (© adrenalinapura - stock.adobe.com)
In A Nutshell
- Some modern humans inherited a Neanderthal version of the growth hormone receptor gene through ancient interbreeding.
- In lab-engineered cells, the Neanderthal version drove 39% faster growth and stronger internal growth signaling than the human version.
- People who carry the variant today tend to be slightly taller and heavier, carry more muscle, and show facial traits like a shorter jaw and higher odds of overbite.
- The gene is rare in Europe but far more common in East and South Asia, reaching about 24% in Pakistan.
Some people today carry a growth-regulating gene inherited from Neanderthals. New research shows the gene makes cells grow faster in lab models, is linked to more muscle mass, and shapes facial features consistent with Neanderthal anatomy.
A study published in Current Biology found that a variant of the growth hormone receptor gene, carried by some modern humans due to ancient interbreeding with Neanderthals, produces a stronger cellular growth signal than the standard human version. The physical differences that show up in carriers today, from body size to jaw shape, trace back to that one signal running hotter.
Neanderthals lived across western Asia and Europe before going extinct around 42,000 years ago, but their DNA lives on in people today. Those with non-African ancestry carry roughly 2% Neanderthal DNA on average, from ancient encounters between the two groups. This research zeroes in on one stretch of that DNA with measurable effects on the body, though nearby genes may also play a role, and it is just one piece of a larger picture.
A Neanderthal Growth Gene Left Its Mark on the Receptor
Neanderthals were not just older humans. They had a robust build, prominent brow ridges, barrel-shaped rib cages, greater muscle mass, and shorter tooth roots than modern humans. Scientists have long suspected genetics drove these differences, but pinning down which genes were responsible has been difficult.
Researchers focused on growth hormone, produced by the pituitary gland, which plays a central role in how bones, muscles, and cartilage develop. When overactive in modern humans, it causes acromegaly, marked by enlarged bones and muscle mass; when underactive, it leads to a form of dwarfism. Examining genes across three high-quality Neanderthal genomes, the team found meaningful differences in the growth hormone receptor gene.
All three Neanderthal genomes carried two changes in the receptor’s protein-coding sequence, plus a deletion with its own separate evolutionary history. These changes appeared consistently in the high-quality genomes and were absent from the sub-Saharan African genomes examined, one clue that the version found in people today came from Neanderthals through ancient interbreeding.
Cells With the Neanderthal Gene Grew 39% Faster
To find out what these changes actually do, researchers used a mouse cell line that depends on external signals to grow and does not naturally produce the growth hormone receptor. Engineering the cells to carry either version let scientists directly compare how each performed.
Cells with the Neanderthal receptor grew faster when exposed to pituitary growth hormone, ending up 39% more numerous after five days. The whole effect traced back to one tiny swap in the receptor, at a spot researchers call position 561, which revved up the cell’s internal growth signal by 22% and pushed the growth rate itself up by 6%.
One finding stood out: exposed to placental growth hormone, made during pregnancy, the two receptors showed no difference at all. Whatever makes the Neanderthal version more responsive only kicks in after birth. The authors think this might trace back to the physical demands of childbirth itself, though they’re careful to call that an educated guess rather than a proven mechanism. That pattern holds up elsewhere too: carriers show no differences in birth weight or childhood measurements up to age 11, but the gap shows up clearly once they reach adulthood.
Carriers Today Have More Muscle and Neanderthal-Like Facial Traits
Using data from more than 1.1 million adults across five genetic databases, plus a birth study and MRI scans, researchers built a detailed picture of what carrying this variant means for the body.
Adults with the variant average 0.30 centimeters taller and 285 grams heavier per copy. Most of that extra weight looks like muscle rather than fat: carriers showed about 150 grams more muscle in the arms and legs, plus more lean tissue packed into the torso. Hips were a bit bigger too, and carriers actually ran leaner overall, pointing to muscle and bone rather than added fat.
Facial differences were also detectable. Carriers tend to have a shorter distance between the jaw joint and jaw corner, averaging 3.6 millimeters shorter per copy across four studies, and were more likely to have an overbite, with roughly 2.8 times the odds of non-carriers. Some studies found shorter tooth roots in carriers too, a trait noted in early examinations of Neanderthal remains.
The Neanderthal Gene Spread Widely, and Its Effects Are Real but Modest
This variant is rare in Europe, at just 0.5%, but climbs fast heading east: 15% in East Asia, 20% in South Asia, and as high as 24% in Pakistan. Tracking it through nearly 10,000 ancient genomes going back 10,000 years shows those numbers have barely budged, suggesting nothing has been actively pushing the gene up or down over that stretch.
A single amino acid swap, carried from a species extinct for tens of thousands of years, is statistically linked to differences in muscle, height, weight, and face shape in millions of people today. The lab work backs up the connection, though it doesn’t prove the gene causes every trait on its own. Either way, it’s a small, concrete reminder that the distant past still shapes bodies now.
Paper Notes
Limitations
By the authors’ own description, the study takes a targeted approach, focusing on one hormonal pathway, and does not address the full range of genetic factors that shaped Neanderthal growth biology. Some analyses relied on smaller external datasets with limited statistical precision. The cell-based experiments used an isolated laboratory model that may not capture how the receptor behaves in real human tissues across different developmental stages. The researchers also note that nearby genes within the same inherited DNA block could contribute to some of the observed physical traits, and they cannot fully rule that out. Additionally, the GHR gene variant’s effects may depend on dietary and broader physiological contexts.
Funding and Disclosures
The study was supported by the Max Planck Foundation, the Max Planck Society, the Knut and Alice Wallenberg Foundation, the Swedish Research Council, the Swedish Brain Foundation, the Okinawa Institute of Science and Technology, the NOMIS Foundation, the Groschinskys Minnesfond, Cornell’s, Philip-Sörensson’s, Åhlén’s and Hedlund’s Foundations, and the Novo Nordisk Foundation. Additional support was provided for NMR facilities through Villum Fonden and the Novo Nordisk Foundation. The Wellcome Trust funded work from co-authors at the Wellcome Sanger Institute. Born in Bradford was supported by a joint grant from the UK Medical Research Council and the UK Economic and Social Science Research Council, the British Heart Foundation, a Wellcome Infrastructure Grant, and the National Institute for Health Research. The Australian Government supported work conducted at the Translational Research Institute. The authors declared no competing interests.
Publication Details
Paper Title: Increased signaling of the Neanderthal growth hormone receptor | Authors: Philipp Kanis, Miriam Berreiter, Daniel Sieme, Olivia Wootton, Xiang-Chun Ju, Nicholas E. Holzwart, David Ziliang Hu, Shu Tadaka, Makiko Taira, Kengo Kinoshita, Richard Ågren, Johan G. Olsen, Tomislav Maricic, Hilary C. Martin, Birthe B. Kragelund, Svante Pääbo, Andrew J. Brooks, and Hugo Zeberg | Journal: Current Biology, Volume 36, August 17, 2026 | DOI: https://doi.org/10.1016/j.cub.2026.07.025 | Corresponding authors: Philipp Kanis ([email protected]) and Hugo Zeberg ([email protected])







