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      Ancient Transposable Elements Transformed the Uterine Regulatory Landscape and Transcriptome during the Evolution of Mammalian Pregnancy

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          SUMMARY

          A major challenge in biology is determining how evolutionarily novel characters originate; however, mechanistic explanations for the origin of new characters are almost completely unknown. The evolution of pregnancy is an excellent system in which to study the origin of novelties because mammals preserve stages in the transition from egg laying to live birth. To determine the molecular bases of this transition, we characterized the pregnant/gravid uterine transcriptome from tetrapods to trace the evolutionary history of uterine gene expression. We show that thousands of genes evolved endometrial expression during the origins of mammalian pregnancy, including genes that mediate maternal-fetal communication and immunotolerance. Furthermore, thousands of cis-regulatory elements that mediate decidualization and cell-type identity in decidualized stromal cells are derived from ancient mammalian transposable elements (TEs). Our results indicate that one of the defining mammalian novelties evolved from DNA sequences derived from ancient mammalian TEs coopted into hormone-responsive regulatory elements distributed throughout the genome.

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          The significance of responses of the genome to challenge.

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            Mice lacking progesterone receptor exhibit pleiotropic reproductive abnormalities.

            Although progesterone has been recognized as essential for the establishment and maintenance of pregnancy, this steroid hormone has been recently implicated to have a functional role in a number of other reproductive events. The physiological effects of progesterone are mediated by the progesterone receptor (PR), a member of the nuclear receptor superfamily of transcription factors. In most cases the PR is induced by estrogen, implying that many of the in vivo effects attributed to progesterone could also be the result of concomitantly administered estrogen. Therefore, to clearly define those physiological events that are specifically attributable to progesterone in vivo, we have generated a mouse model carrying a null mutation of the PR gene using embryonic stem cell/gene targeting techniques. Male and female embryos homozygous for the PR mutation developed normally to adulthood. However, the adult female PR mutant displayed significant defects in all reproductive tissues. These included an inability to ovulate, uterine hyperplasia and inflammation, severely limited mammary gland development, and an inability to exhibit sexual behavior. Collectively, these results provide direct support for progesterone's role as a pleiotropic coordinator of diverse reproductive events that together ensure species survival.
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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
                101573691
                39703
                Cell Rep
                Cell Rep
                Cell reports
                2211-1247
                19 May 2015
                29 January 2015
                3 February 2015
                03 February 2016
                : 10
                : 4
                : 551-561
                Affiliations
                [1 ]Department of Human Genetics, The University of Chicago, 920 East 58 th Street, CLSC 319C, Chicago, IL 60637, USA
                [2 ]Yale Systems Biology Institute and Department of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06511, USA
                [3 ]Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112, USA
                [4 ]Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
                [5 ]The Robinson Institute, School of Molecular and Biomedical Sciences, University of Adelaide, Adelaide, SA 5005, Australia
                [6 ]Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, LMU Munich, Feodor Lynen Strasse 25, 81377 Munich, Germany
                [7 ]Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27705, USA
                [8 ]Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
                [9 ]Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX 77030, USA
                Author notes
                [* ]Correspondence: vjlynch@ 123456uchicago.edu
                [10]

                Present address: Department of Internal Medicine, MSC08 4630, University of New Mexico, 2325 Camino de Saludo NE, CRF 121, Albuquerque, NM 87131-0001, USA

                [11]

                Present address: Department of Genetics, Yale University Medical School, 336 Cedar Street, New Haven, CT 06510, USA

                [12]

                Present address: Animal Physiology, Institute of Agricultural Sciences, ETH Zurich, Universitaetstrasse 2, 8092 Zurich, Switzerland

                Article
                NIHMS689152
                10.1016/j.celrep.2014.12.052
                4447085
                25640180
                136dcccf-b80e-4fe8-be56-fec4382e4c73
                ©2015 The Authors

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/3.0/).

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                Cell biology
                Cell biology

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