eLife (May 2021)
Reduced purine biosynthesis in humans after their divergence from Neandertals
- Vita Stepanova,
- Kaja Ewa Moczulska,
- Guido N Vacano,
- Ilia Kurochkin,
- Xiangchun Ju,
- Stephan Riesenberg,
- Dominik Macak,
- Tomislav Maricic,
- Linda Dombrowski,
- Maria Schörnig,
- Konstantinos Anastassiadis,
- Oliver Baker,
- Ronald Naumann,
- Ekaterina Khrameeva,
- Anna Vanushkina,
- Elena Stekolshchikova,
- Alina Egorova,
- Anna Tkachev,
- Randall Mazzarino,
- Nathan Duval,
- Dmitri Zubkov,
- Patrick Giavalisco,
- Terry G Wilkinson,
- David Patterson,
- Philipp Khaitovich,
- Svante Pääbo
Affiliations
- Vita Stepanova
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation; Institute for Information Transmission Problems, Russian Academy of Sciences, Moscow, Russian Federation
- Kaja Ewa Moczulska
- ORCiD
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
- Guido N Vacano
- ORCiD
- The Eleanor Roosevelt Institute and Knoebel Institute for Healthy Aging, University of Denver, Denver, United States
- Ilia Kurochkin
- ORCiD
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Xiangchun Ju
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany; Okinawa Institute of Science and Technology, Onna-son, Japan
- Stephan Riesenberg
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
- Dominik Macak
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
- Tomislav Maricic
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
- Linda Dombrowski
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
- Maria Schörnig
- ORCiD
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
- Konstantinos Anastassiadis
- ORCiD
- Center for Molecular and Cellular Bioengineering, Biotechnology Center, Technical University Dresden, Dresden, Germany
- Oliver Baker
- Center for Molecular and Cellular Bioengineering, Biotechnology Center, Technical University Dresden, Dresden, Germany
- Ronald Naumann
- Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany
- Ekaterina Khrameeva
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Anna Vanushkina
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Elena Stekolshchikova
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Alina Egorova
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Anna Tkachev
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Randall Mazzarino
- The Eleanor Roosevelt Institute and Knoebel Institute for Healthy Aging, University of Denver, Denver, United States
- Nathan Duval
- The Eleanor Roosevelt Institute and Knoebel Institute for Healthy Aging, University of Denver, Denver, United States
- Dmitri Zubkov
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Patrick Giavalisco
- ORCiD
- Max Planck Institute for Biology of Ageing, Cologne, Germany
- Terry G Wilkinson
- The Eleanor Roosevelt Institute and Knoebel Institute for Healthy Aging, University of Denver, Denver, United States
- David Patterson
- The Eleanor Roosevelt Institute and Knoebel Institute for Healthy Aging, University of Denver, Denver, United States
- Philipp Khaitovich
- ORCiD
- Skolkovo Institute for Science and Technology, Skolkovo, Russian Federation
- Svante Pääbo
- ORCiD
- Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany; Okinawa Institute of Science and Technology, Onna-son, Japan
- DOI
- https://doi.org/10.7554/eLife.58741
- Journal volume & issue
-
Vol. 10
Abstract
We analyze the metabolomes of humans, chimpanzees, and macaques in muscle, kidney and three different regions of the brain. Although several compounds in amino acid metabolism occur at either higher or lower concentrations in humans than in the other primates, metabolites downstream of adenylosuccinate lyase, which catalyzes two reactions in purine synthesis, occur at lower concentrations in humans. This enzyme carries an amino acid substitution that is present in all humans today but absent in Neandertals. By introducing the modern human substitution into the genomes of mice, as well as the ancestral, Neandertal-like substitution into the genomes of human cells, we show that this amino acid substitution contributes to much or all of the reduction of de novo synthesis of purines in humans.
Keywords