34 research outputs found

    Osterix and RUNX2 are Transcriptional Regulators of Sclerostin in Human Bone

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    Sclerostin, encoded by the SOST gene, works as an inhibitor of the Wnt pathway and therefore is an important regulator of bone homeostasis. Due to its potent action as an inhibitor of bone formation, blocking sclerostin activity is the purpose of recently developed antiosteoporotic treatments. Two bone-specific transcription factors, RUNX2 and OSX, have been shown to interact and co-ordinately regulate the expression of bone-specific genes. Although it has been recently shown that sclerostin is targeted by OSX in mice, there is currently no information of whether this is also the case in human cells. We have identified SP-protein family and AML1 consensus binding sequences at the human SOST promoter and have shown that OSX, together with RUNX2, binds to a specific region close to the transcription start site. Furthermore, we show that OSX and RUNX2 activate SOST expression in a co-ordinated manner in vitro and that SOST expression levels show a significant positive correlation with OSX/ RUNX2 expression levels in human bone. We also confirmed previous results showing an association of several SOST/RUNX2 polymorphisms with bone mineral density

    Guidelines for the definition of operational management units

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    The objective of fisheries management is the sustainable exploitation of the fish resources over the extent of their spatial distribution. Along with the Common Fisheries Policy (CFP) objectives, the socio-economic viability of the fisheries exploiting the resource is also to be achieved. To reach these aims, managers need to define the management units they are going to work with. For the purpose of GEPETO project, we define a management unit (MU) as the set of fishing fleets exploiting a common pool of fish resources with strong spatial overlapping and sharing of habitats, which make them being typically fished together. In other words, a MU is the set of fishing fleets exploiting a common fish community over their spatial distribution. MUs have to be defined by the fish community, by the spatial range of distribution of the fish community, and by the set of fishing fleets sharing the exploitation of the fish communityL'objectif de gestion de la pĂȘche est l'exploitation durable des ressources halieutiques sur l'Ă©tendue de leur rĂ©partition spatiale. Avec la nouvelle Politique Commune de la pĂȘche (PCP) l' objectif de la viabilitĂ© socio-Ă©conomique des pĂȘcheries exploitant la ressource doit Ă©galement ĂȘtre rĂ©alisĂ©. Pour l'atteindre, les gestionnaires doivent dĂ©finir des unitĂ©s de gestion. Les partenaires du projet GEPETO, dĂ©finissent une unitĂ© de gestion (MU) comme l'ensemble des flottes de pĂȘche exploitant un pool commun de ressources halieutiques disponibles dans des habitats communs, ce qui les rend trĂšs imbriquĂ©es. En d'autres termes, un MU est l'ensemble des flottes de pĂȘche exploitant une communautĂ© de poissons ordinaires sur leur rĂ©partition spatiale. La MU peu ĂȘtre dĂ©finie par la communautĂ© de poissons, par la gamme spatiale de la distribution de la communautĂ© de poissons, et par l'ensemble des flottes de pĂȘche qui partagent l'exploitation de la communautĂ© de poissons

    Genetic connectivity and hybridization with its siter species challenge the current management paradigm of white anglerfish (Lophius piscatorius)

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    Understanding the inter and intraspecific dynamics of fish populations is essential to promote effective management and conservation actions and to predict adaptation to changing conditions. This is possible through the analysis of thousands of genetic markers, which has proven useful to resolve connectivity among populations. Here, we have tackled this issue in the white anglerfish (Lophius piscatorius), which inhabits the Northeast Atlantic and Mediterranean Sea and coexists with its morphologically almost identical sister species, the black anglerfish (L. budegassa). Our genetic analyses based on 16,000 SNP markers and 700 samples reveal that i) the white anglerfish from the Mediterranean Sea and the Atlantic Ocean are genetically isolated, but that no differentiation can be observed within the later, and that ii) black and white anglerfish naturally hybridize, resulting in a population of about 20% of, most likely sterile, hybrids in some areas. These findings challenge the current paradigm of white anglerfish management, which considers three independent management units within the North East Atlantic and assumes that all mature fish have reproductive potential. Additionally, the northwards distribution of both species, likely due to temperature raises, calls for further monitoring of the abundance and distribution of hybrids to anticipate the effects of climate change in the interactions between both species and their potential resilience

    A GHEP-ISFG collaborative study on the genetic variation of 38 autosomal indels for human identification in different continental populations

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    A collaborative effort was carried out by the Spanish and Portuguese Speaking Working Group of the International Society for Forensic Genetics (GHEP-ISFG) to promote knowledge exchange between associate laboratories interested in the implementation of indel-based methodologies and build allele frequency databases of 38 indels for forensic applications. These databases include populations from different countries that are relevant for identification and kinship investigations undertaken by the participating laboratories. Before compiling population data, participants were asked to type the 38 indels in blind samples from annual GHEP-ISFG proficiency tests, using an amplification protocol previously described. Only laboratories that reported correct results contributed with population data to this study. A total of 5839 samples were genotyped from 45 different populations from Africa, America, East Asia, Europe and Middle East. Population differentiation analysis showed significant differences between most populations studied from Africa and America, as well as between two Asian populations from China and East Timor. Low FST values were detected among most European populations. Overall diversities and parameters of forensic efficiency were high in populations from all continents.Instituto Multidisciplinario de BiologĂ­a CelularFacultad de Ciencias Naturales y Muse

    Do patients diagnosed with a neurological disease present increased risk of suicide?

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    Introduction: Neurological diseases are the leading cause of disability and the second leading cause of death worldwide. Physical and psychological pain, despair, and disconnection with the environment are observed after the diagnosis of numerous neurological processes, particularly neurodegenerative diseases. Development: A higher risk of suicide is observed in patients with such common neurological diseases as epilepsy, migraine, and multiple sclerosis, as well as in those with such degenerative disorders as Alzheimer disease, Huntington disease, amyotrophic lateral sclerosis, and Parkinson’s disease. In most cases, suicidal ideation appears in the early stages after diagnosis, in the presence of disabling symptoms, and/or in patients with psychiatric comorbidities (often associated with these neurological diseases). Conclusions: Effective suicide prevention in this population group requires assessment of the risk of suicide mainly in newly diagnosed patients, in patients showing unmistakable despair or disabling symptoms, and in patients presenting psychiatric comorbidities (especially depressive symptoms). It is essential to train specialists to detect warning signs in order that they may adopt a suitable approach and determine when psychiatric assessment is required. Resumen: IntroducciĂłn: Las enfermedades neurolĂłgicas representan la principal causa de discapacidad y la segunda causa de muerte a nivel mundial. El dolor fĂ­sico y psicolĂłgico, la desesperanza y la desconexiĂłn con el medio estĂĄn presentes tras el diagnĂłstico de numerosos procesos neurolĂłgicos y especialmente de las enfermedades neurodegenerativas. Desarrollo: Existe un mayor riesgo de suicidio en pacientes con enfermedades neurolĂłgicas comunes como la epilepsia, la migraña y la esclerosis mĂșltiple, asĂ­ como en quienes padecen trastornos degenerativos como la enfermedad de Alzheimer, la enfermedad de Huntington, la esclerosis lateral amiotrĂłfica o la enfermedad de Parkinson. En la mayorĂ­a de los casos, la ideaciĂłn suicida aparece en la etapa prĂłxima al diagnĂłstico, ante sintomatologĂ­a invalidante, y/o en pacientes que presentan comorbilidad psiquiĂĄtrica (a menudo asociada con dichas dolencias neurolĂłgicas). Conclusiones: Para una prevenciĂłn efectiva del suicidio en este grupo de la poblaciĂłn debe evaluarse el riesgo principalmente en pacientes reciĂ©n diagnosticados, ante la expresiĂłn de marcada desesperanza, ante sintomatologĂ­a invalidante y en pacientes que presentan comorbilidad psiquiĂĄtrica (especialmente sĂ­ntomas depresivos). La formaciĂłn de los especialistas para detectar signos de alerta es fundamental tanto para que puedan hacer un correcto abordaje como para que sean capaces de determinar cuĂĄndo es necesaria la valoraciĂłn de un especialista en psiquiatrĂ­a
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