20 research outputs found

    A Three-Stage Colonization Model for the Peopling of the Americas

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    Background: We evaluate the process by which the Americas were originally colonized and propose a three-stage model that integrates current genetic, archaeological, geological, and paleoecological data. Specifically, we analyze mitochondrial and nuclear genetic data by using complementary coalescent models of demographic history and incorporating nongenetic data to enhance the anthropological relevance of the analysis. Methodology/Findings: Bayesian skyline plots, which provide dynamic representations of population size changes over time, indicate that Amerinds went through two stages of growth <40,000 and <15,000 years ago separated by a long period of population stability. Isolation-with-migration coalescent analyses, which utilize data from sister populations to estimate a divergence date and founder population sizes, suggest an Amerind population expansion starting <15,000 years ago. Conclusions/Significance: These results support a model for the peopling of the New World in which Amerind ancestors diverged from the Asian gene pool prior to 40,000 years ago and experienced a gradual population expansion as they moved into Beringia. After a long period of little change in population size in greater Beringia, Amerinds rapidly expanded into the Americas <15,000 years ago either through an interior ice-free corridor or along the coast. This rapid colonization of the New World was achieved by a founder group with an effective population size of <1,000–5,400 individuals. Our model presents a detailed scenario for the timing and scale of the initial migration to the Americas, substantially refines th

    MAPK-Activated Protein Kinase 2 Is Required for Mouse Meiotic Spindle Assembly and Kinetochore-Microtubule Attachment

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    MAPK-activated protein kinase 2 (MK2), a direct substrate of p38 MAPK, plays key roles in multiple physiological functions in mitosis. Here, we show for the first time the unique distribution pattern of MK2 in meiosis. Phospho-MK2 was localized on bipolar spindle minus ends and along the interstitial axes of homologous chromosomes extending over centromere regions and arm regions at metaphase of first meiosis (MI stage) in mouse oocytes. At metaphase of second meiosis (MII stage), p-MK2 was localized on the bipolar spindle minus ends and at the inner centromere region of sister chromatids as dots. Knockdown or inhibition of MK2 resulted in spindle defects. Spindles were surrounded by irregular nondisjunction chromosomes, which were arranged in an amphitelic or syntelic/monotelic manner, or chromosomes detached from the spindles. Kinetochore–microtubule attachments were impaired in MK2-deficient oocytes because spindle microtubules became unstable in response to cold treatment. In addition, homologous chromosome segregation and meiosis progression were inhibited in these oocytes. Our data suggest that MK2 may be essential for functional meiotic bipolar spindle formation, chromosome segregation and proper kinetochore–microtubule attachments

    GJ 3090 b: one of the most favourable mini-Neptune for atmospheric characterisation

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    We report the detection of GJ 3090 b (TOI-177.01), a mini-Neptune on a 2.9-day orbit transiting a bright (K = 7.3 mag) M2 dwarf located at 22 pc. The planet was identified by the Transiting Exoplanet Survey Satellite and was confirmed with the High Accuracy Radial velocity Planet Searcher radial velocities. Seeing-limited photometry and speckle imaging rule out nearby eclipsing binaries. Additional transits were observed with the LCOGT, Spitzer, and ExTrA telescopes. We characterise the star to have a mass of 0.519 ± 0.013 M⊙ and a radius of 0.516 ± 0.016 R⊙. We modelled the transit light curves and radial velocity measurements and obtained a planetary mass of 3.34 ± 0.72 ME, a radius of 2.13 ± 0.11 RE, and a mean density of 1.89−0.45+0.52 g cm−3. The low density of the planet implies the presence of volatiles, and its radius and insolation place it immediately above the radius valley at the lower end of the mini-Neptune cluster. A coupled atmospheric and dynamical evolution analysis of the planet is inconsistent with a pure H–He atmosphere and favours a heavy mean molecular weight atmosphere. The transmission spectroscopy metric of 221−46+66 means that GJ 3090 b is the second or third most favorable mini-Neptune after GJ 1214 b whose atmosphere may be characterised. At almost half the mass of GJ 1214 b, GJ 3090 b is an excellent probe of the edge of the transition between super-Earths and mini-Neptunes. We identify an additional signal in the radial velocity data that we attribute to a planet candidate with an orbital period of 13 days and a mass of 17.1−3.2+8.9 ME, whose transits are not detected

    Macrophage migration inhibitory factor and DJ-1 in gastric cancer: differences between high-incidence and low-incidence areas

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    background: There is a need for sensitive and specific blood-borne markers for the detection of gastric cancer. Raised serum macrophage inhibitory factor (MIF) levels have been proposed as a marker for gastric cancer diagnosis but, to date, studies have only encompassed patients from high-incidence areas. methods: We have compared the serum concentration of MIF in a large cohort of UK and Japanese gastric cancer patients, together with appropriate control subjects (age and gender matched). Carcinoembryonic antigen and H. pylori IgG were also measured, as was DJ-1, a novel candidate protein biomarker identified by analysis of gastric cancer cell line secretomes. results: Marked elevations of the serum concentration of MIF and DJ-1 were seen in Japanese patients with gastric cancer compared with Japanese controls, a trend not seen in the UK cohort. These results could not be accounted for by differences in age, disease stage or H. pylori status. conclusion: In regions of high, but not low incidence of gastric cancer, both MIF and DJ-1 have elevated serum concentrations in gastric cancer patients, compared with controls. This suggests that differing mechanisms of disease pathogenesis may be at play in high- and low-incidence regions
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