Los telómeros y el origen de la enfermedad

Este artículo recoge la presentación que la autora llevó a cabo de su carrera científica en el Foro de Encuentros, en Madrid, en Febrero de 2016En el presente texto se recoge la descripción de la trayectoria científica de María A. Blasco, Directora del Centro Nacional de Investigaciones Oncológicas e investigadora española de prestigio internacional, contada por la propia autora, a través de un conjunto de breves apuntes o hitos que han ido jalonando esa carrera científica, enormemente prolífica y cargada de interés científico y social, la cual comenzó después de finalizar su licenciatura en Ciencias Biológicas en la Universidad Autónoma de Madrid, en cuyo Centro de Biología Molecular inició su andadura científica de la mano de Margarita Salas, prestigiosa científica de reconocimiento mundial y a quien entrevistó Encuentros Multidisciplinares en el año 2000, entrevista publicada en el Vol. II nº 1 de esta revista. Aparte de la importancia de su contenido, publicamos este texto como un ejemplo que puede servir como referencia para jóvenes investigadores o universitarios que están planteándose iniciar una carrera investigador

Generation of mice with longer and better preserved telomeres in the absence of genetic manipulations.

Although telomere length is genetically determined, mouse embryonic stem (ES) cells with telomeres of twice the normal size have been generated. Here, we use such ES cells with ‘hyper-long’ telomeres, which also express green fluorescent protein (GFP), to generate chimaeric mice containing cells with both hyper-long and normal telomeres. We show that chimaeric mice contain GFP-positive cells in all mouse tissues, display normal tissue histology and normal survival. Both hyper-long and normal telomeres shorten with age, but GFP-positive cells retain longer telomeres as mice age. Chimaeric mice with hyper-long telomeres also accumulate fewer cells with short telomeres and less DNA damage with age, and express lower levels of p53. In highly renewing compartments, such as the blood, cells with hyper-long telomeres are longitudinally maintained or enriched with age. We further show that wound-healing rates in the skin are increased in chimaeric mice. Our work demonstrates that mice with functional, longer and better preserved telomeres can be generated without the need for genetic manipulations, such as TERT overexpression.post-print3240 K

Data Sources as a Driver for Market‑Oriented Tourism Organizations: a Bibliometric Perspective

This paper presents a conceptual framework that accurately represents the current and future perspectives of data-driven companies in tourism by means of an analysis of the data sources used in the data-driven tourism research literature, as well as the research topics to which they are applied. For this purpose, a bibliometric analysis of data-driven tourism research is carried out. The framework of the study is all tourism-related publications whose research was based on data sources during the period 1982–2020. The results show some of the basic bibliometric performance indicators and the maps of science. The main themes of research interest are identified, and the conceptual evolution is obtained based on these maps. Three major thematic areas are identified: tourism research topics, information sources, and data analysis techniques. Based on these three thematic areas, the conceptual model of data architecture and processes of a data-driven organization in the tourism sector are obtained. An additional qualitative analysis of the three thematic areas is performedCRUE-CSIC agreement with Springer Natur

Are we studying the right populations to understand suicide?

International audienc

Suv4-20h deficiency results in telomere elongation and derepression of telomere recombination

Mammalian telomeres have heterochromatic features, including trimethylated histone H3 at lysine 9 (H3K9me3) and trimethylated histone H4 at lysine 20 (H4K20me3). In addition, subtelomeric DNA is hypermethylated. The enzymatic activities responsible for these modifications at telomeres are beginning to be characterized. In particular, H4K20me3 at telomeres could be catalyzed by the novel Suv4-20h1 and Suv4-20h2 histone methyltransferases (HMTases). In this study, we demonstrate that the Suv4-20h enzymes are responsible for this histone modification at telomeres. Cells deficient for Suv4-20h2 or for both Suv4-20h1 and Suv4-20h2 show decreased levels of H4K20me3 at telomeres and subtelomeres in the absence of changes in H3K9me3. These epigenetic alterations are accompanied by telomere elongation, indicating a role for Suv4-20h HMTases in telomere length control. Finally, cells lacking either the Suv4-20h or Suv39h HMTases show increased frequencies of telomere recombination in the absence of changes in subtelomeric DNA methylation. These results demonstrate the importance of chromatin architecture in the maintenance of telomere length homeostasis and reveal a novel role for histone lysine methylation in controlling telomere recombination

Effect of potential formation on the electrochemical behaviour of a highly-alloyed austenitic stainless steel in contaminated phosphoric acid at different temperatures

The electrochemical behaviour of the highly alloyed austenitic stainless steel UNS N08031 (Alloy 31) in a contaminated phosphoric acid solution is studied using potentiodynamic curves, EIS and Mott–Shottky. The relative stability of the films formed on Alloy 31 has been studied after a pre-passivated treatment at 0.3, 0.5, 0.8 and 1 VAg/AgCl, potentials within the passive domain. The protection of Alloy 31 was provided by the inner oxide film, while the outer film was more defective. The electronic-semiconducting properties of the passive films have been correlated to corrosion resistance. Passivated Alloy 31 at 0.8 VAg/AgCl showed lower concentration of charge carriers, which beneficially affects the protecting and electronic properties of the passive oxide film.The authors wish to express their gratitude to the MAEC of Spain (PCI Mediterraneo C/8196/07, C/018046/08, D/023608/09 and D/030177/10), to Programa de Apoyo a la Investigacion y Desarrollo de la UPV (PAID-06-09), to the Generalitat Valenciana (GV/2011/093) for the financial support and to Dra. Asuncion Jaime for her translation assistance.Escrivá Cerdán, C.; Blasco Tamarit, ME.; García García, DM.; García Antón, J.; Guenbour, A. (2012). Effect of potential formation on the electrochemical behaviour of a highly-alloyed austenitic stainless steel in contaminated phosphoric acid at different temperatures. Electrochimica Acta. 80:248-256. https://doi.org/10.1016/j.electacta.2012.07.012S2482568

Relationship Between the Quorum Network (Sensing/Quenching) and Clinical Features of Pneumonia and Bacteraemia Caused by A. baumannii

Acinetobacter baumannii (Ab) is one of the most important pathogens associated with nosocomial infections, especially pneumonia. Interest in the Quorum network, i.e., Quorum Sensing (QS)/Quorum Quenching (QQ), in this pathogen has grown in recent years. The Quorum network plays an important role in regulating diverse virulence factors such as surface motility and bacterial competition through the type VI secretion system (T6SS), which is associated with bacterial invasiveness. In the present study, we investigated 30 clinical strains of A. baumannii isolated in the “II Spanish Study of A. baumannii GEIH-REIPI 2000-2010” (Genbank Umbrella Bioproject PRJNA422585), a multicentre study describing the relationship between the Quorum network in A. baumannii and the development of pneumonia and associated bacteraemia. Expression of the aidA gene (encoding the AidA protein, QQ enzyme) was lower (P < 0.001) in strains of A. baumannii isolated from patients with bacteraemic pneumonia than in strains isolated from patients with non-bacteraemic pneumonia. Moreover, aidA expression in the first type of strain was not regulated in the presence of environmental stress factors such as the 3-oxo-C12-HSL molecule (substrate of AidA protein, QQ activation) or H2O2 (inhibitor of AidA protein, QS activation). However, in the A. baumannii strains isolated from patients with non-bacteraemic pneumonia, aidA gene expression was regulated by stressors such as 3-oxo-C12-HSL and H2O2. In an in vivo Galleria mellonella model of A. baumannii infection, the A. baumannii ATCC 17978 strain was associated with higher mortality (100% at 24 h) than the mutant, abaI-deficient, strain (carrying a synthetase enzyme of Acyl homoserine lactone molecules) (70% at 24 h). These data suggest that the QS (abaR and abaI genes)/QQ (aidA gene) network affects the development of secondary bacteraemia in pneumonia patients and also the virulence of A. baumannii.National Plan for Scientific ResearchTechnological Development and Innovation PI16/01163ISCIII-Deputy General Directorate for Evaluation and Promotion of Research-European Regional Development Fund A way of Making EuropeInstituto de Salud Carlos IIIMiguel Servet Research Programme SERGAS and ISCIIIXunta de Galicia (GAIN, Axencia de Innovación