Tuesday, December 23, 2014

Nature Cell Biology contents: January 2015 Volume 17 Number 1, pp 1 - 105

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Nature Cell Biology

TABLE OF CONTENTS

January 2015 Volume 17, Issue 1

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Articles
Letter
Corrigenda
Retraction
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News and Views

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Ironing out VPS34 inhibition   pp1 - 3
Timothy Marsh and Jayanta Debnath
doi:10.1038/ncb3089
The class III phosphoinositide 3-kinase VPS34 regulates autophagosome formation. Three groups have developed VPS34 inhibitors and shown their utility in investigating and defining autophagic processes.

Solving the centriole disengagement puzzle   pp3 - 5
Andrew M. Fry
doi:10.1038/ncb3087
The microcephaly protein, Cep215, contributes to the engagement of duplicated centrioles in interphase. Now two distinct pools of Cep215 at centrosomes are identified, one bound to Cep68 and the other to pericentrin. Plk1-mediated degradation of Cep68 and separase-mediated cleavage of pericentrin release both pools of Cep215, thereby promoting centriole disengagement.

See also: Article by Pagan et al.

Hippo signalling directs intestinal fate   pp5 - 6
Marie Le Bouteiller and Kim B. Jensen
doi:10.1038/ncb3086
Hippo signalling has been associated with many important tissue functions including the regulation of organ size. In the intestinal epithelium differing functions have been proposed for the effectors of Hippo signalling, YAP and TAZ1. These are now shown to have a dual role in the intestinal epithelium, regulating both stem cell proliferation and differentiation along a specific secretory lineage.

See also: Article by Imajo et al.

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Articles

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Dual role of YAP and TAZ in renewal of the intestinal epithelium   pp7 - 19
Masamichi Imajo, Miki Ebisuya and Eisuke Nishida
doi:10.1038/ncb3084
Imajo and colleagues report that the Hippo signalling pathway components YAP and TAZ act via TEAD to promote intestinal stem/progenitor cell proliferation and via Klf4 to trigger their differentiation.

AMBRA1 links autophagy to cell proliferation and tumorigenesis by promoting c-Myc dephosphorylation and degradation   pp20 - 30
Valentina Cianfanelli, Claudia Fuoco, Mar Lorente, Maria Salazar, Fabio Quondamatteo et al.
doi:10.1038/ncb3072
mTOR signalling both inhibits autophagy and promotes cell proliferation. Cecconi and colleagues report that AMBRA1 links these two processes by facilitating dephosphorylation and degradation of the proto-oncogene c-Myc.

Degradation of Cep68 and PCNT cleavage mediate Cep215 removal from the PCM to allow centriole separation, disengagement and licensing   pp31 - 43
Julia K. Pagan, Antonio Marzio, Mathew J. K. Jones, Anita Saraf, Prasad V. Jallepalli et al.
doi:10.1038/ncb3076
Pagano and colleagues find that Plk1 and the E3 ubiquitin ligase SCFβTrCP mediate degradation of the centrosome cohesion protein Cep68 and show this mediates removal of Cep215 from the PCM and subsequent centriole separation in late mitosis.

Identification of nuclear hormone receptor pathways causing insulin resistance by transcriptional and epigenomic analysis   pp44 - 56
Sona Kang, Linus T. Tsai, Yiming Zhou, Adam Evertts, Su Xu et al.
doi:10.1038/ncb3080
Rosen and colleagues perform epigenomic and transcriptomic analyses of insulin-resistant cells, and report that the vitamin D receptor and glucocorticoid receptor mediate transcriptional responses that promote insulin resistance.

White-to-brown metabolic conversion of human adipocytes by JAK inhibition   pp57 - 67
Annie Moisan, Youn-Kyoung Lee, Jitao David Zhang, Carolyn S. Hudak, Claas A. Meyer et al.
doi:10.1038/ncb3075
Moisan, Cowan and colleagues perform a small-molecule screen to identify compounds that promote white-to-brown adipocyte conversion in vitro. They report that two inhibitors of the JAK–STAT signalling pathway stimulate browning of human adipocytes.

STRIPAK components determine mode of cancer cell migration and metastasis   pp68 - 80
Chris D. Madsen, Steven Hooper, Melda Tozluoglu, Andreas Bruckbauer, Georgina Fletcher et al.
doi:10.1038/ncb3083
Sahai and colleagues delineate a pathway through which components of the STRIPAK complex promote amoeboid cancer cell migration by regulating the linkage of the actomyosin network to the plasma membrane.

The Rho GTPase Rnd1 suppresses mammary tumorigenesis and EMT by restraining Ras-MAPK signalling   pp81 - 94
Tomoyo Okada, Surajit Sinha, Ilaria Esposito, Gaia Schiavon, Miguel A. López-Lago et al.
doi:10.1038/ncb3082
Giancotti and colleagues report that the Rnd1 Rho GTPase suppresses the epithelial–mesenchymal transition and mammary tumorigenesis by inhibiting Ras-MAPK signalling through a Plexin B1–Rap1–p120 Ras-GAP signalling axis.

Letter

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Hypoxia regulates Hippo signalling through the SIAH2 ubiquitin E3 ligase   pp95 - 103
Biao Ma, Yan Chen, Ling Chen, Hongcheng Cheng, Chenglong Mu et al.
doi:10.1038/ncb3073
Wu and colleagues report that under hypoxic conditions the LATS2 kinase is targeted for degradation by the SIAH2 ubiquitin ligase, leading to inhibition of the Hippo kinase cascade and activation of YAP, which promotes tumour growth.

Corrigenda

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Corrigendum: MicroRNAs are transported in plasma and delivered to recipient cells by high-density lipoproteins   p104
Kasey C. Vickers, Brian T. Palmisano, Bassem M. Shoucri, Robert D. Shamburek and Alan T. Remaley
doi:10.1038/ncb3074

Corrigendum: MXL-3 and HLH-30 transcriptionally link lipolysis and autophagy to nutrient availability   p104
Eyleen J. O'Rourke and Gary Ruvkun
doi:10.1038/ncb3085

Retraction

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Retraction: Wolfram syndrome 1 and adenylyl cyclase 8 interact at the plasma membrane to regulate insulin production and secretion   p105
Sonya G. Fonseca, Fumihiko Urano, Gordon C. Weir, Jesper Gromada and Mark Burcin
doi:10.1038/ncb3088

Editorial note

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Editorial note: Integrating insulin secretion and ER stress in pancreatic β-cells   p105
Katleen Lemaire and Frans Schuit
doi:10.1038/ncb3093

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