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      Cerebral cortex expansion and folding: what have we learned?

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          Abstract

          One of the most prominent features of the human brain is the fabulous size of the cerebral cortex and its intricate folding. Cortical folding takes place during embryonic development and is important to optimize the functional organization and wiring of the brain, as well as to allow fitting a large cortex in a limited cranial volume. Pathological alterations in size or folding of the human cortex lead to severe intellectual disability and intractable epilepsy. Hence, cortical expansion and folding are viewed as key processes in mammalian brain development and evolution, ultimately leading to increased intellectual performance and, eventually, to the emergence of human cognition. Here, we provide an overview and discuss some of the most significant advances in our understanding of cortical expansion and folding over the last decades. These include discoveries in multiple and diverse disciplines, from cellular and molecular mechanisms regulating cortical development and neurogenesis, genetic mechanisms defining the patterns of cortical folds, the biomechanics of cortical growth and buckling, lessons from human disease, and how genetic evolution steered cortical size and folding during mammalian evolution .

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          The complete genome sequence of a Neandertal from the Altai Mountains

          We present a high-quality genome sequence of a Neandertal woman from Siberia. We show that her parents were related at the level of half siblings and that mating among close relatives was common among her recent ancestors. We also sequenced the genome of a Neandertal from the Caucasus to low coverage. An analysis of the relationships and population history of available archaic genomes and 25 present-day human genomes shows that several gene flow events occurred among Neandertals, Denisovans and early modern humans, possibly including gene flow into Denisovans from an unknown archaic group. Thus, interbreeding, albeit of low magnitude, occurred among many hominin groups in the Late Pleistocene. In addition, the high quality Neandertal genome allows us to establish a definitive list of substitutions that became fixed in modern humans after their separation from the ancestors of Neandertals and Denisovans.
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            The delayed rise of present-day mammals.

            Did the end-Cretaceous mass extinction event, by eliminating non-avian dinosaurs and most of the existing fauna, trigger the evolutionary radiation of present-day mammals? Here we construct, date and analyse a species-level phylogeny of nearly all extant Mammalia to bring a new perspective to this question. Our analyses of how extant lineages accumulated through time show that net per-lineage diversification rates barely changed across the Cretaceous/Tertiary boundary. Instead, these rates spiked significantly with the origins of the currently recognized placental superorders and orders approximately 93 million years ago, before falling and remaining low until accelerating again throughout the Eocene and Oligocene epochs. Our results show that the phylogenetic 'fuses' leading to the explosion of extant placental orders are not only very much longer than suspected previously, but also challenge the hypothesis that the end-Cretaceous mass extinction event had a major, direct influence on the diversification of today's mammals.
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              The cell biology of neurogenesis.

              During the development of the mammalian central nervous system, neural stem cells and their derivative progenitor cells generate neurons by asymmetric and symmetric divisions. The proliferation versus differentiation of these cells and the type of division are closely linked to their epithelial characteristics, notably, their apical-basal polarity and cell-cycle length. Here, we discuss how these features change during development from neuroepithelial to radial glial cells, and how this transition affects cell fate and neurogenesis.
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                Author and article information

                Journal
                EMBO J
                EMBO J
                10.1002/(ISSN)1460-2075
                EMBJ
                embojnl
                The EMBO Journal
                John Wiley and Sons Inc. (Hoboken )
                0261-4189
                1460-2075
                07 April 2016
                17 May 2016
                07 April 2016
                : 35
                : 10 ( doiID: 10.1002/embj.v35.10 )
                : 1021-1044
                Affiliations
                [ 1 ] Instituto de NeurocienciasConsejo Superior de Investigaciones Científicas & Universidad Miguel Hernández Sant Joan d'AlacantSpain
                Author notes
                [*] [* ]Corresponding author. Tel: +34 965 919245; E‐mail: vborrell@ 123456umh.es
                [†]

                These authors contributed equally to this work

                Author information
                http://orcid.org/0000-0002-7833-3978
                Article
                EMBJ201593701
                10.15252/embj.201593701
                4868950
                27056680
                704e7d63-f961-49fc-9037-90e67d611891
                © 2016 The Authors. Published under the terms of the CC BY NC ND 4.0 license

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs 4.0 License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 15 December 2015
                : 23 February 2016
                : 17 March 2016
                Page count
                Pages: 24
                Funding
                Funded by: Spanish Ministry of Economy and Competitivity (MINECO)
                Funded by: European Union Seventh Framework Programme
                Award ID: DESIRE 602531
                Funded by: MINECO
                Award ID: BFU2012‐33473
                Funded by: European Research Council
                Award ID: StG309633
                Categories
                Review
                Review
                Custom metadata
                2.0
                embj201593701
                17 May 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.7 mode:remove_FC converted:18.11.2016

                Molecular biology
                evolution,ferret,gyrencephaly,humans,neocortex,neuroscience
                Molecular biology
                evolution, ferret, gyrencephaly, humans, neocortex, neuroscience

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