Tuesday, November 6, 2012

Nature Cell Biology contents: November 2012 Volume 14 Number 11, pp 1113 - 1231

Nature Cell Biology

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TABLE OF CONTENTS

November 2012 Volume 14, Issue 11

Editorial
Review
News and Views
Research Highlights
Articles
Letter
Corrigendum
Erratum

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Editorial

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The Lasker Awards: motors take centre stage   p1113
doi:10.1038/ncb2618
Michael Sheetz, James Spudich and Ronald Vale have been awarded the prestigious Albert Lasker Basic Medical Research Award for their work on cytoskeletal motors. Nature Cell Biology joins the scientific community in congratulating the awardees and in celebrating the importance of basic research in furthering scientific endeavour.

Review

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The functions of microRNAs in pluripotency and reprogramming   pp1114 - 1121
Trevor R. Leonardo, Heather L. Schultheisz, Jeanne F. Loring and Louise C. Laurent
doi:10.1038/ncb2613
Pluripotent stem cells (PSCs) express a distinctive set of microRNAs (miRNAs). Many of these miRNAs have similar targeting sequences and are predicted to regulate downstream targets cooperatively. These enriched miRNAs are involved in the regulation of the unique PSC cell cycle, and there is increasing evidence that they also influence other important characteristics of PSCs, including their morphology, epigenetic profile and resistance to apoptosis. Detailed studies of miRNAs and their targets in PSCs should help to parse the regulatory networks that underlie developmental processes and cellular reprogramming.

News and Views

Top

Setting Snail2's pace during EMT   pp1122 - 1123
Haritha Mathsyaraja and Michael C. Ostrowski
doi:10.1038/ncb2616
Epithelial to mesenchymal transition (EMT) is a fundamental process in both development and cancer progression. The transcription factor Elf5 is now reported as an upstream regulator of the key EMT inducer Snail2, and is shown to regulate the earliest known rewiring events required for tumour cell invasiveness and metastasis.

See also: Article by Chakrabarti et al.

Atypical E2Fs drive atypical cell cycles   pp1124 - 1125
Joy H. Meserve and Robert J. Duronio
doi:10.1038/ncb2609
It is well documented that polyploid cells exist in mammalian tissues such as the placenta and liver, but their function and the mechanisms for their formation have remained elusive. Two studies now identify a role for atypical E2F transcription factors in promoting polyploidy in mammals and challenge present theories about the function of polyploidy.

See also: Article by Pandit et al. | Article by Chen et al.

The amorphous pericentriolar cloud takes shape   pp1126 - 1128
Jens Lüders
doi:10.1038/ncb2617
The pericentriolar material (PCM), the microtubule-organizing component of the centrosome, contains a multitude of proteins and is commonly described as an amorphous cloud surrounding the centrioles. However, the days of the PCM as an unstructured matrix are numbered. Using super-resolution microscopy, several reports have now revealed remarkable domain organization within the PCM.

See also: Article by Lawo et al. | Article by Mennella et al.

Research Highlights

Opo opposes Numb in the eye | Chaperoning tumour bioenergetics | miR-211 negotiates life and death decisions | Aged muscle drives stem cell demise


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Articles

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Multipotent and unipotent progenitors contribute to prostate postnatal development   pp1131 - 1138
Marielle Ousset, Alexandra Van Keymeulen, Gaëlle Bouvencourt, Neha Sharma, Younes Achouri, Benjamin D. Simons and Cédric Blanpain
doi:10.1038/ncb2600
Blanpain and colleagues use inducible genetic lineage tracing to identify and follow the progenitors responsible for the development of the prostate glandular epithelium. They find that multipotent progenitors are initially able to differentiate into the three lineages that make up the prostate, with a later switch to distinct pools of unipotent basal and luminal stem cells.

Nanog-dependent feedback loops regulate murine embryonic stem cell heterogeneity   pp1139 - 1147
Ben D. MacArthur, Ana Sevilla, Michel Lenz, Franz-Josef Müller, Berhard M. Schuldt, Andreas A. Schuppert, Sonya J. Ridden, Patrick S. Stumpf, Miguel Fidalgo, Avi Ma’ayan, Jianlong Wang and Ihor R. Lemischka
doi:10.1038/ncb2603
Lemischka and colleagues examine the effects of transient Nanog downregulation on the components of the pluripotent transcriptional regulatory network using single-cell gene expression analysis and modelling approaches. They observe that the initial changes induced by loss of Nanog are stochastic and reversible upon Nanog restoration, owing to the presence of feedback loops in the pluripotency network. Prolonged loss of Nanog compromises these feedback loops and reversion to pluripotency cannot be achieved upon Nanog restoration.

Subdiffraction imaging of centrosomes reveals higher-order organizational features of pericentriolar material   pp1148 - 1158
Steffen Lawo, Monica Hasegan, Gagan D. Gupta and Laurence Pelletier
doi:10.1038/ncb2591
Centrosomes consist of two centrioles surrounded by pericentriolar material (PCM) that nucleates microtubules. The PCM has been considered as amorphous but, using subdiffraction fluorescence imaging, Pelletier and colleagues now reveal the organized structure of human PCM.

See also: News and Views by Lüders

Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization   pp1159 - 1168
V. Mennella, B. Keszthelyi, K. L. McDonald, B. Chhun, F. Kan, G. C. Rogers, B. Huang and D. A. Agard
doi:10.1038/ncb2597
Centrosomes, the microtubule nucleation centre of most cells, consist of two centrioles surrounded by pericentriolar material (PCM). The PCM has been considered as amorphous but, using subdiffraction fluorescence microscopy approaches, Agard and colleagues now reveal the organized structure of the PCM of Drosophila centrosomes.

See also: News and Views by Lüders

β2-syntrophin and Par-3 promote an apicobasal Rac activity gradient at cell–cell junctions by differentially regulating Tiam1 activity   pp1169 - 1180
Natalie A. Mack, Andrew P. Porter, Helen J. Whalley, Juliane P. Schwarz, Richard C. Jones, Azharuddin Sajid Syed Khaja, Anders Bjartell, Kurt I. Anderson and Angeliki Malliri
doi:10.1038/ncb2608
Malliri and colleagues demonstrate that an apicobasal Rac activity gradient at cell–cell junctions is important for tight-junction assembly and establishment of apicobasal polarity. They show that this gradient is generated by the distinct spatial regulation of the Rac activator Tiam1 by β2-syntrophin and Par3.

E2F8 is essential for polyploidization in mammalian cells   pp1181 - 1191
Shusil K. Pandit, Bart Westendorp, Sathidpak Nantasanti, Elsbeth van Liere, Peter C. J. Tooten, Peter W. A. Cornelissen, Mathilda J. M. Toussaint, Wouter H. Lamers and Alain de Bruin
doi:10.1038/ncb2585
It is not fully understood how polyploidy is regulated in mammals, as the liver is one of only a few tissues in which it occurs. De Bruin and colleagues demonstrate that gene repression through the E2F8 transcription factor, antagonized by E2F1, is required for polyploidization in mice. They also find that loss of polyploidy does not influence liver differentiation or regeneration.

See also: News and Views by Meserve & Duronio

Canonical and atypical E2Fs regulate the mammalian endocycle   pp1192 - 1202
Hui-Zi Chen, Madhu M. Ouseph, Jing Li, Thierry Pécot, Veda Chokshi, Lindsey Kent, Sooin Bae, Morgan Byrne, Camille Duran, Grant Comstock, Prashant Trikha, Markus Mair, Shantibhusan Senapati, Chelsea K. Martin, Sagar Gandhi, Nicholas Wilson, Bin Liu, Yi-Wen Huang, John C. Thompson, Sundaresan Raman, Shantanu Singh, Marcelo Leone, Raghu Machiraju, Kun Huang, Xiaokui Mo, Soledad Fernandez, Ilona Kalaszczynska, Debra J. Wolgemuth, Piotr Sicinski, Tim Huang, Victor Jin and Gustavo Leone
doi:10.1038/ncb2595
In mammals, polyploidy is only seen in liver hepatocytes and in trophoblast giant cells in the placenta. Leone and colleagues now show that ploidy is controlled in an antagonistic fashion by canonical E2F transcriptional activators and atypical E2F7 and E2F8 repressors, through the control of G2/M-associated genes.

See also: News and Views by Meserve & Duronio

Liver cancer initiation is controlled by AP-1 through SIRT6-dependent inhibition of survivin    pp1203 - 1211
Lihua Min, Yuan Ji, Latifa Bakiri, Zhixin Qiu, Jin Cen, Xiaotao Chen, Lingli Chen, Harald Scheuch, Hai Zheng, Lunxiu Qin, Kurt Zatloukal, Lijian Hui and Erwin F. Wagner
doi:10.1038/ncb2590
Wagner and colleagues show that cancer cell survival during liver cancer initiation depends on inhibition of c-Fos-induced apoptosis, through the repression of survivin expression by c-Jun and SIRT6.

Elf5 inhibits the epithelial–mesenchymal transition in mammary gland development and breast cancer metastasis by transcriptionally repressing Snail2    pp1212 - 1222
Rumela Chakrabarti, Julie Hwang, Mario Andres Blanco, Yong Wei, Martin Luka?išin, Rose-Anne Romano, Kirsten Smalley, Song Liu, Qifeng Yang, Toni Ibrahim, Laura Mercatali, Dino Amadori, Bruce G. Haffty, Satrajit Sinha and Yibin Kang
doi:10.1038/ncb2607
Kang and colleagues show that the transcription factor Elf5 controls the epithelial–mesenchymal transition (EMT) during development and in metastasis, by repressing the expression of Snail2/Slug, a key EMT-inducing factor.

See also: News and Views by Mathsyaraja & Ostrowski

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Letter

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PARP16 is a tail-anchored endoplasmic reticulum protein required for the PERK- and IRE1α-mediated unfolded protein response   pp1223 - 1230
Miri Jwa and Paul Chang
doi:10.1038/ncb2593
Chang and colleagues reveal that the poly(ADP-ribose) polymerase PARP16 participates in the endoplasmic reticulum (ER) stress response. They report that PARP16 is a transmembrane ER protein that PARsylates and activates PERK and IRE1α in response to ER stress.

Corrigendum

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Integrins β1 and β3 exhibit distinct dynamic nanoscale organizations inside focal adhesions   p1231
Olivier Rossier, Vivien Octeau, Jean-Baptiste Sibarita, Cécile Leduc, Béatrice Tessier, Deepak Nair, Volker Gatterdam, Olivier Destaing, Corinne Albigès-Rizo, Robert Tampé, Laurent Cognet, Daniel Choquet, Brahim Lounis and Grégory Giannone
doi:10.1038/ncb2620

Erratum

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The data deluge   p1231
doi:10.1038/ncb2626

Top
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