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      Genome analysis reveals insights into physiology and longevity of the Brandt’s bat Myotis brandtii

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          Abstract

          Bats account for one-fifth of mammalian species, are the only mammals with powered flight, and are among the few animals that echolocate. The insect-eating Brandt’s bat ( Myotis brandtii) is the longest-lived bat species known to date (lifespan exceeds 40 years) and, at 4–8 g adult body weight, is the most extreme mammal with regard to disparity between body mass and longevity. Here we report sequencing and analysis of the Brandt’s bat genome and transcriptome, which suggest adaptations consistent with echolocation and hibernation, as well as altered metabolism, reproduction and visual function. Unique sequence changes in growth hormone and insulin-like growth factor 1 receptors are also observed. The data suggest that an altered growth hormone/insulin-like growth factor 1 axis, which may be common to other long-lived bat species, together with adaptations such as hibernation and low reproductive rate, contribute to the exceptional lifespan of the Brandt’s bat.

          Abstract

          Bats account for 20 per cent of all mammals, these are the only mammals with powered flight, and are among the few animals that echolocate. Here, Seim et al. sequence the genome of the long-lived (>40 years) Brandt’s bat, Myotis brandtii and provide clues to its evolution, longevity and other traits.

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          Most cited references38

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          Why do we age?

          The evolutionary theory of ageing explains why ageing occurs, giving valuable insight into the mechanisms underlying the complex cellular and molecular changes that contribute to senescence. Such understanding also helps to clarify how the genome shapes the ageing process, thereby aiding the study of the genetic factors that influence longevity and age-associated diseases.
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            The evolution of maximum body size of terrestrial mammals.

            The extinction of dinosaurs at the Cretaceous/Paleogene (K/Pg) boundary was the seminal event that opened the door for the subsequent diversification of terrestrial mammals. Our compilation of maximum body size at the ordinal level by sub-epoch shows a near-exponential increase after the K/Pg. On each continent, the maximum size of mammals leveled off after 40 million years ago and thereafter remained approximately constant. There was remarkable congruence in the rate, trajectory, and upper limit across continents, orders, and trophic guilds, despite differences in geological and climatic history, turnover of lineages, and ecological variation. Our analysis suggests that although the primary driver for the evolution of giant mammals was diversification to fill ecological niches, environmental temperature and land area may have ultimately constrained the maximum size achieved.
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              The Genetics of Vitamin C Loss in Vertebrates

              Vitamin C (ascorbic acid) plays important roles as an anti-oxidant and in collagen synthesis. These important roles, and the relatively large amounts of vitamin C required daily, likely explain why most vertebrate species are able to synthesize this compound. Surprisingly, many species, such as teleost fishes, anthropoid primates, guinea pigs, as well as some bat and Passeriformes bird species, have lost the capacity to synthesize it. Here, we review the genetic bases behind the repeated losses in the ability to synthesize vitamin C as well as their implications. In all cases so far studied, the inability to synthesize vitamin C is due to mutations in the L-gulono-γ-lactone oxidase (GLO) gene which codes for the enzyme responsible for catalyzing the last step of vitamin C biosynthesis. The bias for mutations in this particular gene is likely due to the fact that losing it only affects vitamin C production. Whereas the GLO gene mutations in fish, anthropoid primates and guinea pigs are irreversible, some of the GLO pseudogenes found in bat species have been shown to be reactivated during evolution. The same phenomenon is thought to have occurred in some Passeriformes bird species. Interestingly, these GLO gene losses and reactivations are unrelated to the diet of the species involved. This suggests that losing the ability to make vitamin C is a neutral trait.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                20 August 2013
                : 4
                : 2212
                Affiliations
                [1 ]Division of Genetics, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School , Boston, Massachusetts 02115, USA
                [2 ]Department of Bioinspired Science, Ewha Womans University , Seoul 120-750, South Korea
                [3 ]BGI-Shenzhen , Shenzhen 518083, China
                [4 ]Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen , Copenhagen DK-2200, Denmark
                [5 ]University of Nebraska , Lincoln, Nebraska 68588, USA
                [6 ]Kirov State Center for Distance Education of Children , Kirov 610006, Russia
                [7 ]Institute of Biology, Komi Science Center, Russian Academy of Sciences , Syktyvkar 167982, Russia
                [8 ]Rodent Histopathology Laboratory, Harvard Medical School , Boston, Massachusetts 02115, USA
                [9 ]Syktyvkar State University , Syktyvkar 167001, Russia
                [10 ]Moscow Institute of Physics and Technology , Dolgoprudny 141700, Russia
                [11 ]Department of Biology, University of Copenhagen , Copenhagen DK-2200, Denmark
                [12 ]These authors contributed equally to this work
                Author notes
                Article
                ncomms3212
                10.1038/ncomms3212
                3753542
                23962925
                5461e660-2924-4e75-8562-0b1a46574e80
                Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

                History
                : 20 December 2012
                : 26 June 2013
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