Catálogo de publicaciones - revistas

<jats:p>The centrosome provides an intracellular anchor for the cytoskeleton, regulating cell division, cell migration, and cilia formation. We used spatial proteomics to elucidate protein interaction networks at the centrosome of human induced pluripotent stem cell–derived neural stem cells (NSCs) and neurons. Centrosome-associated proteins were largely cell type–specific, with protein hubs involved in RNA dynamics. Analysis of neurodevelopmental disease cohorts identified a significant overrepresentation of NSC centrosome proteins with variants in patients with periventricular heterotopia (PH). Expressing the PH-associated mutant pre-mRNA-processing factor 6 (PRPF6) reproduced the periventricular misplacement in the developing mouse brain, highlighting missplicing of transcripts of a microtubule-associated kinase with centrosomal location as essential for the phenotype. Collectively, cell type–specific centrosome interactomes explain how genetic variants in ubiquitous proteins may convey brain-specific phenotypes.</jats:p>

<jats:p> The molecular basis of interindividual clinical variability upon infection with <jats:italic>Staphylococcus aureus</jats:italic> is unclear. We describe patients with haploinsufficiency for the linear deubiquitinase OTULIN, encoded by a gene on chromosome 5p. Patients suffer from episodes of life-threatening necrosis, typically triggered by <jats:italic>S. aureus</jats:italic> infection. The disorder is phenocopied in patients with the 5p− (Cri-du-Chat) chromosomal deletion syndrome. OTULIN haploinsufficiency causes an accumulation of linear ubiquitin in dermal fibroblasts, but tumor necrosis factor receptor–mediated nuclear factor κB signaling remains intact. Blood leukocyte subsets are unaffected. The OTULIN-dependent accumulation of caveolin-1 in dermal fibroblasts, but not leukocytes, facilitates the cytotoxic damage inflicted by the staphylococcal virulence factor α-toxin. Naturally elicited antibodies against α-toxin contribute to incomplete clinical penetrance. Human OTULIN haploinsufficiency underlies life-threatening staphylococcal disease by disrupting cell-intrinsic immunity to α-toxin in nonleukocytic cells. </jats:p>

<jats:p>A hallmark of meiosis is chromosomal pairing, which requires telomere tethering and rotation on the nuclear envelope through microtubules, driving chromosome homology searches. Telomere pulling toward the centrosome forms the “zygotene chromosomal bouquet.” Here, we identified the “zygotene cilium” in oocytes. This cilium provides a cable system for the bouquet machinery and extends throughout the germline cyst. Using zebrafish mutants and live manipulations, we demonstrate that the cilium anchors the centrosome to counterbalance telomere pulling. The cilium is essential for bouquet and synaptonemal complex formation, oogenesis, ovarian development, and fertility. Thus, a cilium represents a conserved player in zebrafish and mouse meiosis, which sheds light on reproductive aspects in ciliopathies and suggests that cilia can control chromosomal dynamics.</jats:p>

<jats:p>Increased government scrutiny of cross-border university research relationships, tightened export controls on technologies, and strengthened national regimes regulating technology-related foreign direct investment are now priorities for most democracies. These policy changes are motivated by the common goal of shoring up economic and national security. But the approaches are neither uniform nor harmonized, even among the relatively homogeneous G7 nations, undermining cross-border research and development (R&amp;D) collaboration. When the leaders of G7 meet in late June in Schloss Elmau, Germany, they should make it a priority to coordinate controls on knowledge flows and technology. They need to act together to demonstrate how democracies can counter illicit activities for acquiring technologies.</jats:p>

<jats:p>As the war in Ukraine enters its fourth month, Russian forces continue to destroy the nation’s scientific institutions and infrastructure, signaling Russia’s intent to obliterate the future for Ukraine. In Kharkiv, for instance, the renowned Institute of Physics and Technology and its newly built Neutron Source nuclear facility have been heavily damaged. Even the Plant Production Institute with its underground national seed bank—one of the world’s largest—has been bombed. At the Chernobyl nuclear labs, Russian forces have looted or destroyed hundreds of computers, radiation dosimeters, and irreplaceable software and equipment. Although the response to each international science crisis is necessarily unique, the US National Academy of Sciences is once again joining with international and regional partners to support beleaguered colleagues, as it did last year in the successful extraction and resettlement of Afghanistan scientists at risk from the Taliban. To that end, the national science academies of Poland, Ukraine, and the United States recently convened a meeting of leaders from several national science academies (including the presidents of Germany’s Leopoldina science academy, the Royal Danish Academy of Sciences and Letters, and the ALLEA European Federation of Academies of Sciences and Humanities, and leaders from the Royal Society of the United Kingdom) to explore how the global science community can best help Ukraine. The resulting 10-point action plan for the world’s research community aims to help meet several immediate needs and also provide the building blocks for revitalizing Ukrainian science in the future.</jats:p>

<jats:p>Ten years ago, physicists found what they predicted. Little new has followed</jats:p>

<jats:p>Graves in Kyrgyzstan hold early victims of plague that swept medieval Europe</jats:p>

<jats:p>Record-shattering events spur climate attribution advances</jats:p>

<jats:p>Increasing potential for fast, cheap genomes may break open biology’s bottleneck and broaden clinical uses</jats:p>