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18.06.2020 20:00

Human brain size gene triggers bigger brain in monkeys

Katrin Boes Presse und Öffentlichkeitsarbeit
Max-Planck-Institut für molekulare Zellbiologie und Genetik

    Dresden and Japanese researchers show that a human-specific gene causes a larger neocortex in the common marmoset, a non-human primate.

    The expansion of the human brain during evolution, specifically of the neocortex, is linked to our cognitive abilities such as reasoning and language. A certain gene called ARHGAP11B that is only found in humans triggers brain stem cells to form more stem cells, a prerequisite for a bigger brain. Past studies have shown that ARHGAP11B, when expressed in mice and ferrets to unphysiologically high levels, causes an expanded neocortex, but its relevance for primate evolution has been unclear. Researchers at the Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG) in Dresden together with colleagues at the Central Institute for Experimental Animals (CIEA) in Kawasaki and the Keio University in Tokyo, both located in Japan, show now that this human-specific gene, when expressed to physiological levels, causes an enlarged neocortex in the common marmoset, a New World monkey. This suggests that the ARHGAP11B gene may have caused neocortex expansion during human evolution. The researchers published their findings in the journal Science.

    The human neocortex, the evolutionarily youngest part of the cerebral cortex, is about three times bigger than that of our closest relatives, the chimpanzees, and its folding into wrinkles increased during evolution to fit inside the restricted space of the skull. A key question for scientists is how the human neocortex became so big. In a 2015 study, the research group of Wieland Huttner, a founding director of the MPI-CBG, found that under the influence of the human-specific gene ARHGAP11B, mouse embryos produced many more neural progenitor cells and could even undergo folding of their normally unfolded neocortex. The results suggested that the gene ARHGAP11B plays a key role in the evolutionary expansion of the human neocortex.

    The rise of the human-specific gene
    The human-specific gene ARHGAP11B arose through a partial duplication of the ubiquitous gene ARHGAP11A approximately five million years ago along the evolutionary lineage leading to Neanderthals, Denisovans, and present-day humans, and after this lineage had segregated from that leading to the chimpanzee. In a follow-up study in 2016, the research group of Wieland Huttner uncovered a surprising reason why the ARHGAP11B protein contains a sequence of 47 amino acids that is human-specific, not found in the ARHGAP11A protein, and essential for ARHGAP11B's ability to increase brain stem cells. Specifically, a single C-to-G base substitution found in the ARHGAP11B gene leads to the loss of 55 nucleotides from the ARHGAP11B messenger RNA, which causes a shift in the reading frame resulting in the human-specific, functionally critical 47 amino acid sequence. This base substitution probably happened much later than when this gene arose about 5 million years ago, anytime between 1.5 million and 500,000 years ago. Such point mutations are not rare, but in the case of ARHGAP11B its advantages of forming a bigger brain seem to have immediately influenced human evolution.

    The gene’s effect in monkeys
    However, it has been unclear until now if the human-specific gene ARHGAP11B would also cause an enlarged neocortex in non-human primates. To investigate this, the researchers in the group of Wieland Huttner teamed up with Erika Sasaki at the Central Institute for Experimental Animals (CIEA) in Kawasaki and Hideyuki Okano at the Keio University in Tokyo, both located in Japan, who had pioneered the development of a technology to generate transgenic non-human primates. The first author of the study, postdoc Michael Heide, travelled to Japan to work with the colleagues directly on-site. They generated transgenic common marmosets, a New World monkey, that expressed the human-specific gene ARHGAP11B, which they normally do not have, in the developing neocortex. Japan has similarly high ethical standards and regulations regarding animal research and animal welfare as Germany does. The brains of 101-day-old common marmoset fetuses (50 days before the normal birth date) were obtained in Japan and exported to the MPI-CBG in Dresden for detailed analysis. Michael Heide explains: “We found indeed that the neocortex of the common marmoset brain was enlarged and the brain surface folded. Its cortical plate was also thicker than normal. Furthermore, we could see increased numbers of basal radial glia progenitors in the outer subventricular zone and increased numbers of upper-layer neurons, the neuron type that increases in primate evolution.” The researchers had now functional evidence that ARHGAP11B causes an expansion of the primate neocortex.

    Ethical consideration
    Wieland Huttner, who led the study, adds: “We confined our analyses to marmoset fetuses, because we anticipated that the expression of this human-specific gene would affect the neocortex development in the marmoset. In light of potential unforeseeable consequences with regard to postnatal brain function, we considered it a prerequisite – and mandatory from an ethical point of view – to first determine the effects of ARHGAP11B on the development of fetal marmoset neocortex.”

    The researchers conclude that these results suggest that the human-specific ARHGAP11B gene may have caused neocortex expansion in the course of human evolution.

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    About the MPI-CBG
    The Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG) is one of more than 80 institutes of the Max Planck Society, an independent, non-profit organization in Germany. 550 curiosity-driven scientists from over 50 countries ask: How do cells form tissues? The basic research programs of the MPI-CBG span multiple scales of magnitude, from molecular assemblies to organelles, cells, tissues, organs, and organisms.

    About the Central Institute for Experimental Animals (CIEA), Kawasaki, Japan
    The CIEA is a private and independent Non-profit institute, founded in 1952 with the aim of contributing to medical care and medical science based on animal experiments. The institute is developing humanized laboratory animals such as humanized mice and genetically modified common marmosets and investigating analytical methods using imaging instruments.

    Keio University, Tokyo, Japan
    Keio University is a private university located in Minato, Tokyo, Japan. It is known as the oldest institute of modern higher education in Japan. The university has eleven campuses in Tokyo and Kanagawa and ten faculties: Letters, Economics, Law, Business and Commerce, Medicine, Science and Technology, Policy Management, Environment and Information Studies, Nursing and Medical Care, and Pharmacy.

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    Questions to Prof. Wieland B. Huttner (Max Planck Institute of Molecular Cell Biology and Genetics, Dresden) about the publication:

    Michael Heide, Christiane Haffner, Ayako Murayama, Yoko Kurotaki, Haruka
    Shinohara, Hideyuki Okano, Erika Sasaki and Wieland B. Huttner: “Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset”, published by Science, via First Release, 18th June 2020.

    Why did you generate transgenic monkeys in Japan for subsequent analysis?
    Providing evidence that the human-specific gene ARHGAP11B can actually enlarge the developing neocortex of primates requires ARHGAP11B to be expressed in the fetal neocortex of non-human primates. Two non-human primate species, the rhesus monkey and the common marmoset, are appropriate for such studies. Our Japanese colleagues with whom we have collaborated are pioneers in the generation of transgenic common marmosets worldwide and therefore, the generation of the ARHGAP11B-transgenic monkeys for our study took place in Japan.

    How are the animal welfare standards there?
    Just as high as in Germany.

    Are there plans to study animals with this gene modification in later phases of life to investigate the effects on behavior?
    Such experiments are currently neither planned nor in progress.

    What ethical problems would you see in such a case?
    From my personal point of view, I consider it ethically problematic to establish a transgenic monkey line with a human-specific gene, where this gene is passed on from generation to generation via the germ line. If postnatal or adult common marmosets, which express ARHGAP11B in the neocortex, are to be studied for their behavior, such research should be restricted to single, repeatedly generated transgenic monkey individuals rather than creating a transgenic monkey line. In our case we did not only limit our investigations to repeatedly newly generated transgenic common marmoset individuals. We also deliberately limited the analyses to the fetal stage to not get into a situation that could potentially be problematic from an ethical point of view.

    Would such experiments be possible or allowed in Germany?
    Yes, in principle such experiments could be carried out, for example, at the German Primate Centre in Göttingen, provided that the necessary official permits have been obtained.


    Wissenschaftliche Ansprechpartner:

    Wieland Huttner
    +49 (0) 351 210 1500
    huttner@mpi-cbg.de


    Originalpublikation:

    Michael Heide, Christiane Haffner, Ayako Murayama, Yoko Kurotaki, Haruka
    Shinohara, Hideyuki Okano, Erika Sasaki and Wieland B. Huttner: “Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset”, published by Science, via First Release, 18th June 2020.


    Weitere Informationen:

    https://www.mpi-cbg.de/research-groups/current-groups/wieland-huttner/research-f...


    Bilder

    Microscopy image of a section through one brain hemisphere of a 101 day- old ARHGAP11B-transgenic marmoset fetus. Cell nuclei are visualized by DAPI (white). Arrows indicate a sulcus and a gyrus.
    Microscopy image of a section through one brain hemisphere of a 101 day- old ARHGAP11B-transgenic ma ...

    Heide et al. / MPI-CBG

    Wildtype (normal) and ARHGAP11B-transgenic fetal (101 days) marmoset brains. Yellow lines, boundaries of cerebral cortex; white lines, developing cerebellum; arrowheads, folds. Scale bars, 1 mm.
    Wildtype (normal) and ARHGAP11B-transgenic fetal (101 days) marmoset brains. Yellow lines, boundarie ...

    Heide et al. / MPI-CBG


    Merkmale dieser Pressemitteilung:
    Journalisten
    Biologie
    überregional
    Forschungsergebnisse, Wissenschaftliche Publikationen
    Englisch


     

    Microscopy image of a section through one brain hemisphere of a 101 day- old ARHGAP11B-transgenic marmoset fetus. Cell nuclei are visualized by DAPI (white). Arrows indicate a sulcus and a gyrus.


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    Wildtype (normal) and ARHGAP11B-transgenic fetal (101 days) marmoset brains. Yellow lines, boundaries of cerebral cortex; white lines, developing cerebellum; arrowheads, folds. Scale bars, 1 mm.


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