Author
Listed:
- Gayani Senevirathne
(Harvard University)
- Serena C. Fernandopulle
(Harvard University)
- Daniel Richard
(Harvard University
Stanford University)
- Stephanie L. Baumgart
(University of Florida College of Veterinary Medicine)
- Anika Liv Christensen
(Harvard University)
- Matteo Fabbri
(John Hopkins University School of Medicine)
- Jakob Höppner
(Massachusetts General Hospital and Harvard Medical School)
- Harald Jüppner
(Massachusetts General Hospital and Harvard Medical School)
- Peishu Li
(Ohio University Heritage College of Osteopathic Medicine)
- Vivien Bothe
(Museum für Naturkunde)
- Nadia Fröbisch
(Museum für Naturkunde)
- Ian Simcock
(Great Ormond Street Hospital
University College London Great Ormond Street Institute of Child Health
NIHR Great Ormond Street Biomedical Research Centre)
- Owen J. Arthurs
(Great Ormond Street Hospital
University College London Great Ormond Street Institute of Child Health
NIHR Great Ormond Street Biomedical Research Centre)
- Alistair Calder
(Great Ormond Street Hospital)
- Naomi Freilich
(Harvard University)
- Niamh C. Nowlan
(School of Mechanical and Materials Engineering and University College Dublin (UCD) Conway Institute)
- Ian A. Glass
(University of Washington)
- April Craft
(Harvard Medical School
Harvard Stem Cell Institute)
- Terence D. Capellini
(Harvard University
Broad Institute of MIT and Harvard)
Abstract
Bipedalism is a human-defining trait1–3. It is made possible by the familiar, bowl-shaped pelvis, whose short, wide iliac blades curve along the sides of the body to stabilize walking and support internal organs and a large-brained, broad-shouldered baby4–6. The ilium changes compared with living primates are an evolutionary novelty7. However, how this evolution came about remains unknown. Here, using a multifaceted histological, comparative genomic and functional genomic approach, we identified the developmental bases of the morphogenetic shifts in the human pelvis that made bipedalism possible. First, we observe that the human ilium cartilage growth plate underwent a heterotopic shift, residing perpendicular to the orientation present in other primate (and mouse) ilia. Second, we observe heterochronic and heterotopic shifts in ossification that are unlike those in non-human primate ilia or human long bones. Ossification initiates posteriorly, resides externally with fibroblast (and perichondral) cells contributing to osteoblasts, and is delayed compared with other bones in humans and with primate ilia. Underlying these two shifts are regulatory changes in an integrated chondrocyte–perichondral–osteoblast pathway, involving complex hierarchical interactions between SOX9–ZNF521–PTH1R and RUNX2–FOXP1/2. These innovations facilitated further growth of the human pelvis and the unique formation of the ilium among primates.
Suggested Citation
Gayani Senevirathne & Serena C. Fernandopulle & Daniel Richard & Stephanie L. Baumgart & Anika Liv Christensen & Matteo Fabbri & Jakob Höppner & Harald Jüppner & Peishu Li & Vivien Bothe & Nadia Fröbi, 2025.
"The evolution of hominin bipedalism in two steps,"
Nature, Nature, vol. 645(8082), pages 952-963, September.
Handle:
RePEc:nat:nature:v:645:y:2025:i:8082:d:10.1038_s41586-025-09399-9
DOI: 10.1038/s41586-025-09399-9
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