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      Evolution of genetic networks for human creativity

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          Abstract

          The genetic basis for the emergence of creativity in modern humans remains a mystery despite sequencing the genomes of chimpanzees and Neanderthals, our closest hominid relatives. Data-driven methods allowed us to uncover networks of genes distinguishing the three major systems of modern human personality and adaptability: emotional reactivity, self-control, and self-awareness. Now we have identified which of these genes are present in chimpanzees and Neanderthals. We replicated our findings in separate analyses of three high-coverage genomes of Neanderthals. We found that Neanderthals had nearly the same genes for emotional reactivity as chimpanzees, and they were intermediate between modern humans and chimpanzees in their numbers of genes for both self-control and self-awareness. 95% of the 267 genes we found only in modern humans were not protein-coding, including many long-non-coding RNAs in the self-awareness network. These genes may have arisen by positive selection for the characteristics of human well-being and behavioral modernity, including creativity, prosocial behavior, and healthy longevity. The genes that cluster in association with those found only in modern humans are over-expressed in brain regions involved in human self-awareness and creativity, including late-myelinating and phylogenetically recent regions of neocortex for autobiographical memory in frontal, parietal, and temporal regions, as well as related components of cortico-thalamo-ponto-cerebellar-cortical and cortico-striato-cortical loops. We conclude that modern humans have more than 200 unique non-protein-coding genes regulating co-expression of many more protein-coding genes in coordinated networks that underlie their capacities for self-awareness, creativity, prosocial behavior, and healthy longevity, which are not found in chimpanzees or Neanderthals.

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          Most cited references119

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          Initial sequencing and analysis of the human genome.

          The human genome holds an extraordinary trove of information about human development, physiology, medicine and evolution. Here we report the results of an international collaboration to produce and make freely available a draft sequence of the human genome. We also present an initial analysis of the data, describing some of the insights that can be gleaned from the sequence.
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            A default mode of brain function.

            A baseline or control state is fundamental to the understanding of most complex systems. Defining a baseline state in the human brain, arguably our most complex system, poses a particular challenge. Many suspect that left unconstrained, its activity will vary unpredictably. Despite this prediction we identify a baseline state of the normal adult human brain in terms of the brain oxygen extraction fraction or OEF. The OEF is defined as the ratio of oxygen used by the brain to oxygen delivered by flowing blood and is remarkably uniform in the awake but resting state (e.g., lying quietly with eyes closed). Local deviations in the OEF represent the physiological basis of signals of changes in neuronal activity obtained with functional MRI during a wide variety of human behaviors. We used quantitative metabolic and circulatory measurements from positron-emission tomography to obtain the OEF regionally throughout the brain. Areas of activation were conspicuous by their absence. All significant deviations from the mean hemisphere OEF were increases, signifying deactivations, and resided almost exclusively in the visual system. Defining the baseline state of an area in this manner attaches meaning to a group of areas that consistently exhibit decreases from this baseline, during a wide variety of goal-directed behaviors monitored with positron-emission tomography and functional MRI. These decreases suggest the existence of an organized, baseline default mode of brain function that is suspended during specific goal-directed behaviors.
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              Unique features of long non-coding RNA biogenesis and function.

              Long non-coding RNAs (lncRNAs) are a diverse class of RNAs that engage in numerous biological processes across every branch of life. Although initially discovered as mRNA-like transcripts that do not encode proteins, recent studies have revealed features of lncRNAs that further distinguish them from mRNAs. In this Review, we describe special events in the lifetimes of lncRNAs - before, during and after transcription - and discuss how these events ultimately shape the unique characteristics and functional roles of lncRNAs.
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                Author and article information

                Contributors
                crcloninger44@gmail.com
                Journal
                Mol Psychiatry
                Mol Psychiatry
                Molecular Psychiatry
                Nature Publishing Group UK (London )
                1359-4184
                1476-5578
                21 April 2021
                21 April 2021
                2022
                : 27
                : 1
                : 354-376
                Affiliations
                [1 ]GRID grid.4367.6, ISNI 0000 0001 2355 7002, Department of Psychiatry, , Washington University School of Medicine, ; St. Louis, MO USA
                [2 ]GRID grid.4489.1, ISNI 0000000121678994, Department of Computer Science and Artificial Intelligence, , University of Granada, Andalusian Research Institute in Data Science and Computational Intelligence, ; Granada, Spain
                [3 ]GRID grid.10858.34, ISNI 0000 0001 0941 4873, Unit of Psychology, Faculty of Education, , University of Oulu, ; Oulu, Finland
                [4 ]Anthropedia Foundation, St. Louis, MO USA
                [5 ]GRID grid.39382.33, ISNI 0000 0001 2160 926X, The Menninger Clinic, Baylor College of Medicine, and DeBakey VA Medical Center, ; Houston, TX USA
                [6 ]GRID grid.413185.a, ISNI 0000 0001 2353 5102, The Menninger Clinic, ; Houston, TX USA
                [7 ]GRID grid.502801.e, ISNI 0000 0001 2314 6254, Department of Clinical Chemistry, Fimlab Laboratories, and Finnish Cardiovascular Research Center - Tampere, Faculty of Medicine and Health Technology, , Tampere University, ; Tampere, Finland
                [8 ]GRID grid.1374.1, ISNI 0000 0001 2097 1371, Center for Population Health Research, , University of Turku and Turku University Hospital; Research Center of Applied and Preventive Cardiovascular Medicine, University of Turku; Department of Clinical Physiology and Nuclear Medicine, Turku University Hospital, ; Turku, Finland
                [9 ]GRID grid.7737.4, ISNI 0000 0004 0410 2071, Department of Psychology and Logopedics, , University of Helsinki, ; Helsinki, Finland
                [10 ]GRID grid.215352.2, ISNI 0000000121845633, Department of Psychiatry, , University of Texas San Antonio, Long School of Medicine, The Glenn Briggs Institute of Alzheimer’s and Neurodegenerative Disorders, ; San Antonio, TX USA
                [11 ]GRID grid.241963.b, ISNI 0000 0001 2152 1081, American Museum of Natural History, ; New York, NY USA
                Author information
                http://orcid.org/0000-0002-1443-0234
                http://orcid.org/0000-0002-2212-2039
                http://orcid.org/0000-0003-2673-0901
                http://orcid.org/0000-0003-2049-2658
                http://orcid.org/0000-0002-1105-566X
                http://orcid.org/0000-0002-3806-235X
                http://orcid.org/0000-0001-6423-4461
                http://orcid.org/0000-0002-2555-4427
                http://orcid.org/0000-0003-3096-4807
                Article
                1097
                10.1038/s41380-021-01097-y
                8960414
                33879864
                3d36bd71-9787-4faf-8830-03e398183d56
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 30 October 2020
                : 19 March 2021
                : 31 March 2021
                Categories
                Expert Review
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                © The Author(s), under exclusive licence to Springer Nature Limited 2022

                Molecular medicine
                genetics,psychology,neuroscience
                Molecular medicine
                genetics, psychology, neuroscience

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