33. Insulator dysfunction and oncogene activation in IDH mutant gliomas.
作者: William A Flavahan.;Yotam Drier.;Brian B Liau.;Shawn M Gillespie.;Andrew S Venteicher.;Anat O Stemmer-Rachamimov.;Mario L Suvà.;Bradley E Bernstein.
来源: Nature. 2016年529卷7584期110-4页
Gain-of-function IDH mutations are initiating events that define major clinical and prognostic classes of gliomas. Mutant IDH protein produces a new onco-metabolite, 2-hydroxyglutarate, which interferes with iron-dependent hydroxylases, including the TET family of 5'-methylcytosine hydroxylases. TET enzymes catalyse a key step in the removal of DNA methylation. IDH mutant gliomas thus manifest a CpG island methylator phenotype (G-CIMP), although the functional importance of this altered epigenetic state remains unclear. Here we show that human IDH mutant gliomas exhibit hypermethylation at cohesin and CCCTC-binding factor (CTCF)-binding sites, compromising binding of this methylation-sensitive insulator protein. Reduced CTCF binding is associated with loss of insulation between topological domains and aberrant gene activation. We specifically demonstrate that loss of CTCF at a domain boundary permits a constitutive enhancer to interact aberrantly with the receptor tyrosine kinase gene PDGFRA, a prominent glioma oncogene. Treatment of IDH mutant gliomaspheres with a demethylating agent partially restores insulator function and downregulates PDGFRA. Conversely, CRISPR-mediated disruption of the CTCF motif in IDH wild-type gliomaspheres upregulates PDGFRA and increases proliferation. Our study suggests that IDH mutations promote gliomagenesis by disrupting chromosomal topology and allowing aberrant regulatory interactions that induce oncogene expression.
34. A LAIR1 insertion generates broadly reactive antibodies against malaria variant antigens.
作者: Joshua Tan.;Kathrin Pieper.;Luca Piccoli.;Abdirahman Abdi.;Mathilde Foglierini Perez.;Roger Geiger.;Claire Maria Tully.;David Jarrossay.;Francis Maina Ndungu.;Juliana Wambua.;Philip Bejon.;Chiara Silacci Fregni.;Blanca Fernandez-Rodriguez.;Sonia Barbieri.;Siro Bianchi.;Kevin Marsh.;Vandana Thathy.;Davide Corti.;Federica Sallusto.;Peter Bull.;Antonio Lanzavecchia.
来源: Nature. 2016年529卷7584期105-109页
Plasmodium falciparum antigens expressed on the surface of infected erythrocytes are important targets of naturally acquired immunity against malaria, but their high number and variability provide the pathogen with a powerful means of escape from host antibodies. Although broadly reactive antibodies against these antigens could be useful as therapeutics and in vaccine design, their identification has proven elusive. Here we report the isolation of human monoclonal antibodies that recognize erythrocytes infected by different P. falciparum isolates and opsonize these cells by binding to members of the RIFIN family. These antibodies acquired broad reactivity through a novel mechanism of insertion of a large DNA fragment between the V and DJ segments. The insert, which is both necessary and sufficient for binding to RIFINs, encodes the entire 98 amino acid collagen-binding domain of LAIR1, an immunoglobulin superfamily inhibitory receptor encoded on chromosome 19. In each of the two donors studied, the antibodies are produced by a single expanded B-cell clone and carry distinct somatic mutations in the LAIR1 domain that abolish binding to collagen and increase binding to infected erythrocytes. These findings illustrate, with a biologically relevant example, a novel mechanism of antibody diversification by interchromosomal DNA transposition and demonstrate the existence of conserved epitopes that may be suitable candidates for the development of a malaria vaccine.
35. Corrigendum: Hypoxia fate mapping identifies cycling cardiomyocytes in the adult heart.
作者: Wataru Kimura.;Feng Xiao.;Diana C Canseco.;Shalini Muralidhar.;SuWannee Thet.;Helen M Zhang.;Yezan Abderrahman.;Rui Chen.;Joseph A Garcia.;John M Shelton.;James A Richardson.;Abdelrahman M Ashour.;Aroumougame Asaithamby.;Hanquan Liang.;Chao Xing.;Zhigang Lu.;Cheng Cheng Zhang.;Hesham A Sadek.
来源: Nature. 2016年532卷7598期268页 36. Cancer: Oncogene brought into the loop.
Analysis of the 3D structure of DNA in tumour cells reveals how mutations in the IDH1 gene, and associated changes in methyl groups attached to DNA, elevate the expression of cancer-promoting genes.
37. The global spectrum of plant form and function.
作者: Sandra Díaz.;Jens Kattge.;Johannes H C Cornelissen.;Ian J Wright.;Sandra Lavorel.;Stéphane Dray.;Björn Reu.;Michael Kleyer.;Christian Wirth.;I Colin Prentice.;Eric Garnier.;Gerhard Bönisch.;Mark Westoby.;Hendrik Poorter.;Peter B Reich.;Angela T Moles.;John Dickie.;Andrew N Gillison.;Amy E Zanne.;Jérôme Chave.;S Joseph Wright.;Serge N Sheremet'ev.;Hervé Jactel.;Christopher Baraloto.;Bruno Cerabolini.;Simon Pierce.;Bill Shipley.;Donald Kirkup.;Fernando Casanoves.;Julia S Joswig.;Angela Günther.;Valeria Falczuk.;Nadja Rüger.;Miguel D Mahecha.;Lucas D Gorné.
来源: Nature. 2016年529卷7585期167-71页
Earth is home to a remarkable diversity of plant forms and life histories, yet comparatively few essential trait combinations have proved evolutionarily viable in today's terrestrial biosphere. By analysing worldwide variation in six major traits critical to growth, survival and reproduction within the largest sample of vascular plant species ever compiled, we found that occupancy of six-dimensional trait space is strongly concentrated, indicating coordination and trade-offs. Three-quarters of trait variation is captured in a two-dimensional global spectrum of plant form and function. One major dimension within this plane reflects the size of whole plants and their parts; the other represents the leaf economics spectrum, which balances leaf construction costs against growth potential. The global plant trait spectrum provides a backdrop for elucidating constraints on evolution, for functionally qualifying species and ecosystems, and for improving models that predict future vegetation based on continuous variation in plant form and function.
38. Controlling many-body states by the electric-field effect in a two-dimensional material.
作者: L J Li.;E C T O'Farrell.;K P Loh.;G Eda.;B Özyilmaz.;A H Castro Neto.
来源: Nature. 2016年529卷7585期185-9页
To understand the complex physics of a system with strong electron-electron interactions, the ideal is to control and monitor its properties while tuning an external electric field applied to the system (the electric-field effect). Indeed, complete electric-field control of many-body states in strongly correlated electron systems is fundamental to the next generation of condensed matter research and devices. However, the material must be thin enough to avoid shielding of the electric field in the bulk material. Two-dimensional materials do not experience electrical screening, and their charge-carrier density can be controlled by gating. Octahedral titanium diselenide (1T-TiSe2) is a prototypical two-dimensional material that reveals a charge-density wave (CDW) and superconductivity in its phase diagram, presenting several similarities with other layered systems such as copper oxides, iron pnictides, and crystals of rare-earth elements and actinide atoms. By studying 1T-TiSe2 single crystals with thicknesses of 10 nanometres or less, encapsulated in two-dimensional layers of hexagonal boron nitride, we achieve unprecedented control over the CDW transition temperature (tuned from 170 kelvin to 40 kelvin), and over the superconductivity transition temperature (tuned from a quantum critical point at 0 kelvin up to 3 kelvin). Electrically driving TiSe2 over different ordered electronic phases allows us to study the details of the phase transitions between many-body states. Observations of periodic oscillations of magnetoresistance induced by the Little-Parks effect show that the appearance of superconductivity is directly correlated with the spatial texturing of the amplitude and phase of the superconductivity order parameter, corresponding to a two-dimensional matrix of superconductivity. We infer that this superconductivity matrix is supported by a matrix of incommensurate CDW states embedded in the commensurate CDW states. Our results show that spatially modulated electronic states are fundamental to the appearance of two-dimensional superconductivity.
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