 |  |  |  |  | Table of ContentsHave you seen? Articles | Volume 33, Number 21 | Have you seen?  | Recent studies revealed an intimate crosstalk between Hippo/YAP1 and oncogenic RAS signaling in tumors. Complementary data published in The EMBO Journal establish RAS to antagonize Hippo function by regulating YAP protein stability. Vincenzo Corbo, Mariano Ponz‐Sarvise, and David A Tuveson Published online 25.09.2014 |  | A novel mechanism of interaction adhesion receptors is discussed in which integrins are activated by membrane tension generated by uPAR in the absence of integrin‐ligand binding. Ralph Thomas Böttcher and Reinhard Fässler Published online 17.09.2014 |  | The Parkinson's disease‐associated ubiquitin ligase parkin is regulated by the deubiquitinases USP8, USP15 and USP30 — either directly through de‐ubiquitination of parkin or by removing ubiquitin from mitochondrial proteins, ensuring regulation of the ubiquitin signals that trigger mitophagy. Ivan Dikic and Anja Bremm Published online 01.10.2014 |  | A secretory pathway maintains ER proteostasis by targeting misfolded GPI‐anchored proteins to the plasma membrane for subsequent endocytic uptake and lysosomal degradation. Andrés Couve and Claudio Hetz Published online 04.09.2014 | Articles  | Ras antagonises Hippo tumor suppressor activity by direct regulation of YAP‐stability. Ras controls SOCS‐protein expression, channeling YAP into ubiquitin‐dependent degradation. Xin Hong, Hung Thanh Nguyen, Qingfeng Chen, Rui Zhang, Zandra Hagman, P Mathijs Voorhoeve, and Stephen M Cohen |  | Cell adhesion mediated by uPAR and other adhesion receptors triggers non‐canonical integrin activation independent of integrin–ligand interactions. The cross‐talk between adhesion receptors and integrins is mediated by membrane tension. Gian Maria Sarra Ferraris, Carsten Schulte, Valentina Buttiglione, Valentina De Lorenzi, Andrea Piontini, Massimiliano Galluzzi, Alessandro Podestà, Chris D Madsen, and Nicolai Sidenius Published online 28.08.2014 |  | The deubiquitinase USP8 is required for parkin recruitment to mitochondria and thus mitophagy by removing K6‐linked ubiquitin conjugates from parkin hence opposing its auto‐ubiquitination. Thomas M Durcan, Matthew Y Tang, Joëlle R Pérusse, Eman A Dashti, Miguel A Aguileta, Gian‐Luca McLelland, Priti Gros, Thomas A Shaler, Denis Faubert, Benoit Coulombe, and Edward A Fon Published online 12.09.2014 |  | SPP, an intramembrane protease involved in ER signal peptide cleavage, functions in a novel ERAD branch to catalyze proteolysis of the unfolded protein response (UPR) regulator XPB1u in complex with Derlin1 and TRC8. Chia‐yi Chen, Nicole S Malchus, Beate Hehn, Walter Stelzer, Dönem Avci, Dieter Langosch, and Marius K Lemberg Published online 19.09.2014 |  | Maintenance of ‘active’ histone modification patterns and gene expression at an endogenous reporter gene locus requires its processive replication, being affected by G4 DNA formation on the leading strand template close to the transcription start site. Davide Schiavone, Guillaume Guilbaud, Pierre Murat, Charikleia Papadopoulou, Peter Sarkies, Marie‐Noëlle Prioleau, Shankar Balasubramanian, and Julian E Sale |  | A cell‐free model system recapitulating replication of G4 DNA shows that G4 motifs form a transient replication barrier, which is unwound and overcome through the help of the FANCJ/BRIP1 helicase. Pau Castillo Bosch, Sandra Segura‐Bayona, Wouter Koole, Jane T van Heteren, James M Dewar, Marcel Tijsterman, and Puck Knipscheer |  | The molecular interactions between SAGA subunits and its modules are determined using a combination of crosslinking and mass spectrometry together with genetic and biochemical analysis. Yan Han, Jie Luo, Jeffrey Ranish, and Steven Hahn Published online 12.09.2014 |  | X‐ray structures of eIF5B and aEF1A reveal the presence of a monovalent cation in the active site, thus offering insight on the mechanism of GTP hydrolysis and prompting the re‐interpretation of earlier studies on translational GTPases. Bernhard Kuhle and Ralf Ficner Published online 15.09.2014 |  | The chemokine CCL2 and its scavenging receptor ACKR2 antagonistically regulate lymphatic vessel density. This is the result of the developmental control of the proximity of pro‐lymphangiogenic macrophages to lymphatic vessels. Kit M Lee, Renzo Danuser, Jens V Stein, Delyth Graham, Robert JB Nibbs, and Gerard J Graham |  | A RING domain‐like fold within the mouse MEK Kinase 1 polyubiquitylates TAK1‐binding protein 1 (TAB1), a critical adaptor in the TGF‐β signaling pathway, which stimulates Mitogen‐Activated Protein Kinase signaling and is required for correct embryonic stem cell differentiation and tumourigenicity, and for cardiac, testis and B‐cell development in mice in vivo. Nikolaos Charlaftis, Tesha Suddason, Xuefeng Wu, Saba Anwar, Michael Karin, and Ewen Gallagher | |  | | |
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