Friday, October 30, 2015

Nature Cell Biology contents: November 2015 Volume 17 Number 11, pp 1371 - 15120

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Nature Cell Biology


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TABLE OF CONTENTS

November 2015 Volume 17, Issue 11

News and Views
Articles
Letters
Corrigendum
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News and Views

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A mammalian pexophagy target   pp1371 - 1373
Suresh Subramani
doi:10.1038/ncb3253
Protein ubiquitylation in mammals is known to trigger selective autophagy of peroxisomes through a process termed pexophagy. The physiological peroxisomal target for pexophagy-related ubiquitylation has been controversial, but two studies have now identified the protein PEX5 as the real candidate.

Endosomal integrin signals for survival   pp1373 - 1375
Elena Rainero and Jim C. Norman
doi:10.1038/ncb3261
The mechanisms underlying integrin-dependent signalling are a topic of continued study. Endocytosed integrins are now shown to drive assembly of signalling complexes on the cytoplasmic face of endocytic membranes to promote cancer cell survival and increase metastatic capacity following cell detachment.

See also: Article by Alanko et al.

RNF138 joins the HR team   pp1375 - 1377
Simon Bekker-Jensen and Niels Mailand
doi:10.1038/ncb3262
Two studies show that the E3 ubiquitin ligase RNF138 is recruited to DNA double-strand break sites, where it ubiquitylates key repair factors to promote DNA-end resection and homologous recombination. These findings add insights into the multilayered regulatory mechanisms underlying DNA double-strand break repair pathway choice in mammalian cells.

See also: Article by Ismail et al. | Article by Schmidt et al.

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Articles

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Atg5-independent autophagy regulates mitochondrial clearance and is essential for iPSC reprogramming   pp1379 - 1387
Tianhua Ma, Jun Li, Yue Xu, Chen Yu, Tao Xu et al.
doi:10.1038/ncb3256
Ding and colleagues show that somatic cell reprogramming does not depend on Atg5-dependent canonical autophagy, but requires mitochondrial clearance in an Atg5-independent manner downstream of AMPK.

Microtubule-driven nuclear rotations promote meiotic chromosome dynamics   pp1388 - 1400
Nicolas Christophorou, Thomas Rubin, Isabelle Bonnet, Tristan Piolot, Marion Arnaud et al.
doi:10.1038/ncb3249
Huynh and colleagues discover nuclear rotations driven by centrosomes, microtubules and Dynein in Drosophila germ cells, and find that these movements facilitate the pairing of homologous chromosomes.

Heterochromatic breaks move to the nuclear periphery to continue recombinational repair   pp1401 - 1411
Taehyun Ryu, Brett Spatola, Laetitia Delabaere, Katherine Bowlin, Hannah Hopp et al.
doi:10.1038/ncb3258
Chiolo and colleagues find that, in a SUMOylation-dependent manner, heterochromatic double-strand breaks move to the nuclear periphery where Rad51 is recruited to continue repair.

Integrin endosomal signalling suppresses anoikis   pp1412 - 1421
Jonna Alanko, Anja Mai, Guillaume Jacquemet, Kristine Schauer, Riina Kaukonen et al.
doi:10.1038/ncb3250
Ivaska and colleagues report that endocytosed integrins are able to signal from endosomes in an FAK-dependent manner. They further show that endosomal integrin signalling can promote anoikis resistance and lung colonization in cancer cells.

See also: News and Views by Rainero & Norman

Complementary activities of TPX2 and chTOG constitute an efficient importin-regulated microtubule nucleation module   pp1422 - 1434
Johanna Roostalu, Nicholas I. Cade and Thomas Surrey
doi:10.1038/ncb3241
Using TIRF-based in vitro reconstitution assays Surrey and colleagues characterize how chTOG and TPX2 cooperate in microtubule nucleation and find that importins regulate the process.

Competition for actin between two distinct F-actin networks defines a bistable switch for cell polarization   pp1435 - 1445
Alexis J. Lomakin, Kun-Chun Lee, Sangyoon J. Han, Duyen A. Bui, Michael Davidson et al.
doi:10.1038/ncb3246
Lomakin et al. report that the competition for actin between two distinct F-actin networks determines whether epithelial cells remain stationary or migrate, with myosin II inhibiting the migratory polarized phenotype by confining actin in contractile bundles.

The RNF138 E3 ligase displaces Ku to promote DNA end resection and regulate DNA repair pathway choice   pp1446 - 1457
Ismail Hassan Ismail, Jean-Philippe Gagné, Marie-Michelle Genois, Hilmar Strickfaden, Darin McDonald et al.
doi:10.1038/ncb3259
Jackson and colleagues and Hendzel and colleagues reveal that the E3 ligase RNF138 functions in the repair of double-strand breaks by promoting CtIP accumulation and displacement of DNA-PK subunit Ku.

See also: News and Views by Bekker-Jensen & Mailand

Systematic E2 screening reveals a UBE2D–RNF138–CtIP axis promoting DNA repair   pp1458 - 1470
Christine K. Schmidt, Yaron Galanty, Matylda Sczaniecka-Clift, Julia Coates, Satpal Jhujh et al.
doi:10.1038/ncb3260
Jackson and colleagues and Hendzel and colleagues reveal that the E3 ligase RNF138 functions in the repair of double-strand breaks by promoting CtIP accumulation and displacement of DNA-PK subunit Ku.

See also: News and Views by Bekker-Jensen & Mailand

Activator–inhibitor coupling between Rho signalling and actin assembly makes the cell cortex an excitable medium   pp1471 - 1483
William M. Bement, Marcin Leda, Alison M. Moe, Angela M. Kita, Matthew E. Larson et al.
doi:10.1038/ncb3251
Using live imaging of Xenopus and starfish oocytes and embryos undergoing cytokinesis, Bement and colleagues show that anaphase onset promotes cortical waves of Rho and F-actin, which can be modelled by reaction–diffusion dynamics.

6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1–AMPK signalling   pp1484 - 1496
Ruiting Lin, Shannon Elf, Changliang Shan, Hee-Bum Kang, Quanjiang Ji et al.
doi:10.1038/ncb3255
Chen and colleagues report that the third enzyme in the oxidative pentose phosphate pathway (PPP), 6PGD, controls cancer cell proliferation by regulating LKB1–AMPK signalling. Inhibitors of 6PGD decrease tumorigenesis in mouse xenografts.

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Letters

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Lateral adhesion drives reintegration of misplaced cells into epithelial monolayers   pp1497 - 1503
Dan T. Bergstralh, Holly E. Lovegrove and Daniel St Johnston
doi:10.1038/ncb3248
Using live imaging, St Johnston and colleagues show in three Drosophila epithelia that cells born outside the epithelium do not die, but reintegrate, and that lateral adhesion is required for reintegration to occur.

High-speed depolymerization at actin filament ends jointly catalysed by Twinfilin and Srv2/CAP   pp1504 - 1511
Adam B. Johnston, Agnieszka Collins and Bruce L. Goode
doi:10.1038/ncb3252
Goode and colleagues report that Twinfilin and Srv2 cooperate to accelerate depolymerization of actin filaments.

Corrigendum

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Corrigendum: Complementary activities of TPX2 and chTOG constitute an efficient importin-regulated microtubule nucleation module   p1512
Johanna Roostalu, Nicholas I. Cade and Thomas Surrey
doi:10.1038/ncb3265

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