Apoptosis and cell death

Apolist: monthly literature updates for researchers

ApoList – August 2012

Posted by cris on September 2, 2012

——————————–
Bcl-2 family proteins
——————————–

NOXA, a sensor of proteasome integrity, is degraded by 26S proteasomes by an ubiquitin-independent pathway that is blocked by MCL-1
A Craxton, M Butterworth, N Harper, L Fairall, J Schwabe, A Ciechanover and G M Cohen
http://www.nature.com/cdd/journal/v19/n9/abs/cdd201216a.html

BCL2 Suppresses PARP1 Function and Nonapoptotic Cell Death
Chaitali Dutta, Tovah Day, Nadja Kopp, Diederik van Bodegom, Matthew S. Davids, Jeremy Ryan, Liat Bird, Naveen Kommajosyula, Oliver Weigert, Akinori Yoda, Hua Fung, Jennifer R. Brown, Geoffrey I. Shapiro, Anthony Letai, and David M. Weinstock
http://cancerres.aacrjournals.org/cgi/content/abstract/72/16/4193

Bcl-2 is a better ABT-737 target than Bcl-xL or Bcl-w and only Noxa overcomes resistance mediated by Mcl-1, Bfl-1, or Bcl-B
R W Rooswinkel, B van de Kooij, M Verheij and J Borst
http://www.nature.com/cddis/journal/v3/n8/abs/cddis2012109a.html

Correspondence
Is BID required for NOD signalling?
Ueli Nachbur, James E. Vince, Lorraine A. O’Reilly, Andreas Strasser & John Silke
http://www.nature.com/nature/journal/v488/n7412/full/nature11366.html

Yeretssian et al. reply
Garabet Yeretssian, Ricardo G. Correa, Karine Doiron, Patrick Fitzgerald, Christopher P. Dillon, Douglas R. Green, John C. Reed & Maya Saleh
http://www.nature.com/nature/journal/v488/n7412/full/nature11367.html

 
—————————————–
Death receptors-necroptosis
—————————————–

dsRNA induces apoptosis through an atypical death complex associating TLR3 to caspase-8
Y Estornes, F Toscano, F Virard, G Jacquemin, A Pierrot, B Vanbervliet, M Bonnin, N Lalaoui, P Mercier-Gouy, Y Pachéco, B Salaun, T Renno, O Micheau and S Lebecque
http://www.nature.com/cdd/journal/v19/n9/abs/cdd201222a.html

Ubiquitination and degradation of the FADD adaptor protein regulate death receptor-mediated apoptosis and necroptosis
Eun-Woo Lee, Jung-Hoon Kim, Ye-Hyeon Ahn, Jinho Seo, Aram Ko, Manhyung Jeong, Seok-Jun Kim, Jae Y. Ro, Ki-Moon Park, Han-Woong Lee, Eun Jung Park, Kyung-Hee Chun and Jaewhan Song
http://www.nature.com/ncomms/journal/v3/n7/abs/ncomms1981.html

GRIM-19-mediated translocation of STAT3 to mitochondria is necessary for TNF-induced necroptosis
Nataly Shulga and John G. Pastorin
http://jcs.biologists.org/cgi/content/abstract/125/12/2995

RIP1-dependent assembly of a cytosolic cell death complex is required for IAP inhibitor-mediated sensitization for Lexatumumab-induced apoptosis
Farhan Basit, Robin Humphreys, and Simone Fulda
http://www.jbc.org/cgi/content/abstract/M112.398966v1

Oxidative Processing of Latent Fas in the Endoplasmic Reticulum Controls the Strength of Apoptosis
Vikas Anathy, Elle Roberson, Brian Cunniff, James D. Nolin, Sidra Hoffman, Page Spiess, Amy S. Guala, Karolyn G. Lahue, Dylan Goldman, Stevenson Flemer, Albert van der Vliet, Nicholas H. Heintz, Ralph C. Budd, Kenneth D. Tew, and Yvonne M. W. Janssen-Heininger
http://mcb.asm.org/cgi/content/abstract/32/17/3464

The Transmembrane Domains of TNF-Related Apoptosis-Inducing Ligand (TRAIL) Receptors 1 and 2 Co-Regulate Apoptotic Signaling Capacity
Simon Neumann, Tobias Bidon, Marcus Branschädel, Anja Krippner-Heidenreich, Peter Scheurich, Malgorzata Doszczak
http://www.plosone.org/article/info:doi/10.1371/journal.pone.0042526

Cell Death via DR5, but not DR4, Is Regulated by p53 in Myeloma Cells
Sylvanie Surget, David Chiron, Patricia Gomez-Bougie, Géraldine Descamps, Emmanuelle Ménoret, Régis Bataille, Philippe Moreau, Steven Le Gouill, Martine Amiot, and Catherine Pellat-Deceunynck
http://cancerres.aacrjournals.org/cgi/content/abstract/72/17/4562

——————
Caspases
——————

A Genome-Wide RNA Interference Screen Identifies Caspase 4 as a Factor Required for Tumor Necrosis Factor Alpha Signaling
Dorothee Nickles, Christina Falschlehner, Marie Metzig, and Michael Boutros
http://mcb.asm.org/cgi/content/abstract/32/17/3372

Caspase-11 increases susceptibility to Salmonella infection in the absence of caspase-1
Petr Broz, Thomas Ruby, Kamila Belhocine, Donna M. Bouley, Nobuhiko Kayagaki, Vishva M. Dixit & Denise M. Monack
http://www.nature.com/nature/journal/vaop/ncurrent/full/nature11419.html

Quantitative profiling of caspase-cleaved substrates reveals different drug-induced and cell-type patterns in apoptosis
Kazutaka Shimbo, Gerald W. Hsu, Huy Nguyen, Sami Mahrus, Jonathan C. Trinidad, Alma L. Burlingame, and James A. Wells
http://www.pnas.org/content/109/31/12432.abstract?etoc

Fibrils colocalize caspase-3 with procaspase-3 to foster maturation
Julie Anne Zorn, Dennis William Wolan, Nicholas John Agard, and James A. Wells
http://www.jbc.org/cgi/content/abstract/M112.386128v1

Zinc-Mediated Allosteric Inhibition of Caspase-6
Elih M. Velazquez-Delgado and Jeanne A. Hardy
J. Biol. Chem. published 13 August 2012, 10.1074/jbc.M112.397752
http://www.jbc.org/cgi/content/abstract/M112.397752v1

————————
Miscellaneous
————————

Programmed elimination of cells by caspase-independent cell extrusion in C. elegans
Daniel P. Denning, Victoria Hatch & H. Robert Horvitz http://www.nature.com/nature/journal/v488/n7410/full/nature11240.html

Heat shock protein 90α (HSP90α), a substrate and chaperone of DNA-PK necessary for the apoptotic response
Stéphanie Solier, Kurt W. Kohn, Bradley Scroggins, Wanping Xu, Jane Trepel, Leonard Neckers, and Yves Pommier
http://www.pnas.org/content/109/32/12866.abstract?etoc

Annexin A2 and A5 serve as new ligands for C1Q on apoptotic cells
Myriam Martin, Jonatan Leffler, and Anna M. Blom
http://www.jbc.org/cgi/content/abstract/M112.341339v1

——————————————–
Comments / reviews / other
——————————————–

Caspase-3 in the central nervous system: beyond apoptosis
D’Amelio, Sheng, and Cecconi
http://www.cell.com/trends/neurosciences/abstract/S0166-2236%2812%2900115-4

Cell signalling: A necrosome build-up
RIP1–RIP3 complexes form amyloid-like fibrils to promote programmed necrosis.
http://www.nature.com/nrm/journal/v13/n9/full/nrm3415.html

Safety control for apoptotic irreversibility
Marie Dutreix
http://www.pnas.org/content/109/32/12844.extract?etoc

An improved understanding of TNFL/TNFR interactions using structure-based classifications
Cedrik Magis, Almer M. van der Sloot, Luis Serrano, Cedric Notredame
http://www.sciencedirect.com/science/article/pii/S0968000412000771

Mitochondrial Dynamics and Apoptosis—the ER Connection
Suzanne Hoppins, Jodi Nunnari
http://www.sciencemag.org/cgi/content/summary/337/6098/1052

Cell Press Webinar: Imaging the Sustainable Cell
Doug Green, Ana María Cuervo, Ivan Dikic
http://view6.workcast.net/register?pak=9930857197891551

——————————————————————————————————-

——————————————————————————————————-

Advertisements

One Response to “ApoList – August 2012”

  1. cris said

    Reblogged this on Metabolism and cancer articles.

    Like

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

 
%d bloggers like this: