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      Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world? : Function and basis of seasonal coat colour moults

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          The hair follicle as a dynamic miniorgan.

          Hair is a primary characteristic of mammals, and exerts a wide range of functions including thermoregulation, physical protection, sensory activity, and social interactions. The hair shaft consists of terminally differentiated keratinocytes that are produced by the hair follicle. Hair follicle development takes place during fetal skin development and relies on tightly regulated ectodermal-mesodermal interactions. After birth, mature and actively growing hair follicles eventually become anchored in the subcutis, and periodically regenerate by spontaneously undergoing repetitive cycles of growth (anagen), apoptosis-driven regression (catagen), and relative quiescence (telogen). Our molecular understanding of hair follicle biology relies heavily on mouse mutants with abnormalities in hair structure, growth, and/or pigmentation. These mice have allowed novel insights into important general molecular and cellular processes beyond skin and hair biology, ranging from organ induction, morphogenesis and regeneration, to pigment and stem cell biology, cell proliferation, migration and apoptosis. In this review, we present basic concepts of hair follicle biology and summarize important recent advances in the field.
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            Seasonal changes in plasma glucocorticoid concentrations in free-living vertebrates.

            The vertebrate stress response helps animals respond to environmental dangers such as predators or storms. An important component of the stress response is glucocorticoid (GC) release, resulting from activation of the hypothalamic-pituitary-adrenal axis. After release, GCs induce a variety of behavioral and physiological changes that presumably help the animal respond appropriately to the situation. Consequently, GC secretion is often considered an obligatory response to stressful situations. Evidence now indicates, however, that free-living species from many taxa can seasonally modulate GC release. In other words, the magnitudes of both unstressed and stressed GC concentrations change depending upon the time of year. This review examines the growing evidence that GC concentrations in free-living reptiles, amphibians, and birds, but not mammals, are commonly elevated during the breeding season. This evidence is then used to test three hypotheses with different focuses on GC's energetic or behavioral effects, as well as on GC's role in preparing the animal for subsequent stressors. These hypotheses attempt to place annual GC rhythms into a physiological or behavioral context. Integrating seasonal differences in GC concentrations with either different physiological states or different life history stages provides clues to a new understanding of how GCs actually help in survival during stress. Consequently, understanding seasonal modulation of GC release has far-reaching importance for both the physiology of the stress response and the short-term survival of individual animals.
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              A single amino acid mutation contributes to adaptive beach mouse color pattern.

              Natural populations of beach mice exhibit a characteristic color pattern, relative to their mainland conspecifics, driven by natural selection for crypsis. We identified a derived, charge-changing amino acid mutation in the melanocortin-1 receptor (Mc1r) in beach mice, which decreases receptor function. In genetic crosses, allelic variation at Mc1r explains 9.8% to 36.4% of the variation in seven pigmentation traits determining color pattern. The derived Mc1r allele is present in Florida's Gulf Coast beach mice but not in Atlantic coast mice with similar light coloration, suggesting that different molecular mechanisms are responsible for convergent phenotypic evolution. Here, we link a single mutation in the coding region of a pigmentation gene to adaptive quantitative variation in the wild.
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                Author and article information

                Journal
                Biological Reviews
                Biol Rev
                Wiley
                14647931
                March 05 2018
                Affiliations
                [1 ]Wildlife Biology Program; University of Montana; Missoula MT 59812 U.S.A.
                [2 ]Fisheries, Wildlife, and Conservation Biology Program, Department of Forestry and Environmental Resources; North Carolina State University; Raleigh NC 27695 U.S.A.
                [3 ]Institute of Wildlife Biology and Game Management; BOKU - University of Natural Resources and Life Sciences; Vienna 1180 Austria
                [4 ]Division of Biological Sciences; University of Montana; Missoula MT 59812 USA
                [5 ]CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, InBIO Laboratório Associado; Universidade do Porto; Campus Agrário de Vairão, 4485-661 Vairão Portugal
                [6 ]Departamento de Biologia; Faculdade de Ciências da Universidade do Porto; Rua do Campo Alegre, 4169-007 Porto Portugal
                [7 ]Wildlife Biology Program and Office of Research and Creative Scholarship; University of Montana; Missoula MT 59812 USA
                Article
                10.1111/brv.12405
                29504224
                303c60f0-bada-4105-87d9-61fddd1d736e
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://creativecommons.org/licenses/by/4.0/

                http://creativecommons.org/licenses/by/4.0/

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