Friday, January 31, 2014

Nature Cell Biology contents: February 2014 Volume 16 Number 2, pp 127 - 200

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TABLE OF CONTENTS

February 2014 Volume 16, Issue 2

News and Views
Articles
Letter
Corrigendum
Errata
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News and Views

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Lateral junction dynamics lead the way out   pp127 - 129
Martin Behrndt and Carl-Philipp Heisenberg
doi:10.1038/ncb2913
Epithelial cell layers need to be tightly regulated to maintain their integrity and correct function. Cell integration into epithelial sheets is now shown to depend on the N-WASP-regulated stabilization of cortical F-actin, which generates distinct patterns of apical-lateral contractility at E-cadherin-based cell-cell junctions.
See also: Article by Wu et al.

Methyltransferases modulate RNA stability in embryonic stem cells   pp129 - 131
Shuibin Lin and Richard I. Gregory
doi:10.1038/ncb2914
Emerging data support that RNA methylation plays important roles in RNA processing and metabolism. The methyltransferases Mettl3 and Mettl14 are shown to catalyse N6-methyladenosine (m6A) RNA modification in embryonic stem cells (ESCs). This m6A modification controls RNA metabolism and functions to destabilize mRNAs encoding developmental regulators to help sustain ESC self-renewal.
See also: Letter by Wang et al.

Articles

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A polarized Ca2+, diacylglycerol and STIM1 signalling system regulates directed cell migration   pp133 - 144
Feng-Chiao Tsai, Akiko Seki, Hee Won Yang, Arnold Hayer, Silvia Carrasco et al.
doi:10.1038/ncb2906
Meyer and colleagues used live-cell imaging to study the spatial organization of Ca2+ signalling network components during cell migration.

The TRF1-binding protein TERB1 promotes chromosome movement and telomere rigidity in meiosis   pp145 - 156
Hiroki Shibuya, Kei-ichiro Ishiguro and Yoshinori Watanabe
doi:10.1038/ncb2896
Meiotic chromosome movement is needed for homologue pairing and synapsis. Watanabe and colleagues identify TERB1 as a protein needed for telomere mobility and attachment to the nuclear envelope, and for telomere enrichment of meiotic cohesin.

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Enhancing nucleotide metabolism protects against mitochondrial dysfunction and neurodegeneration in a PINK1 model of Parkinson’s disease   pp157 - 166
Roberta Tufi, Sonia Gandhi, Inês P. de Castro, Susann Lehmann, Plamena R. Angelova et al.
doi:10.1038/ncb2901
Mutations in PINK1 cause early-onset Parkinson’s disease. Martins and colleagues find that the expression levels of genes involved in nucleotide metabolism are upregulated in a Drosophila pink1 mutant, and that this affects neuronal mitochondrial DNA synthesis. They find that enhancing nucleotide synthesis through genetics or pharmacological approaches rescues mitochondrial defects associated with PINK1 mutations.

Cortical F-actin stabilization generates apical–lateral patterns of junctional contractility that integrate cells into epithelia   pp167 - 178
Selwin K. Wu, Guillermo A. Gomez, Magdalene Michael, Suzie Verma, Hayley L. Cox et al.
doi:10.1038/ncb2900
Yap and colleagues demonstrate that E-cadherin-based cell–cell junctions exhibit distinct patterns of apical and lateral contractility. They show that N-WASP-dependent stabilization of F-actin mediates increased apical junctional tension, and that modulation of intra-junctional tension differences can promote extrusion of cells from monolayers.
See also: News and Views by Behrndt & Heisenberg

In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators   pp179 - 190
Wen-Hui Lien, Lisa Polak, Mingyan Lin, Kenneth Lay, Deyou Zheng et al.
doi:10.1038/ncb2903
Hair follicle stem cells (HFSCs) regenerate hair in response to Wnt signalling. Fuchs and colleagues use a genome-wide survey to discover that Wnt effectors TCF3, TCF4 and Groucho (TLE) coordinately repress Wnt target genes. They find that although β-catenin is dispensable for HSFC viability and proliferation, it is essential to relieve this repression to initiate hair follicle fate during the hair regeneration cycle.

Letter

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N6-methyladenosine modification destabilizes developmental regulators in embryonic stem cells   pp191 - 198
Yang Wang, Yue Li, Julia I. Toth, Matthew D. Petroski, Zhaolei Zhang et al.
doi:10.1038/ncb2902
N6-methyladenosine (m6A) is an abundant internal modification of messenger RNA (mRNA) that has been reported recently in thousands of mammalian mRNAs and long non-coding RNAs (lncRNAs). Zhao and colleagues identify two methyltransferases responsible for this modification in mammalian cells, and demonstrate that they are required for embryonic stem cell self-renewal maintenance through an effect of the modification on the degradation of developmental regulator transcripts.
See also: News and Views by Lin & Gregory

Corrigendum

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Corrigendum: A genetic screen identies an LKB1-MARK signalling axis controlling the Hippo-YAP pathway   p200
Morvarid Mohseni, Jianlong Sun, Allison Lau, Stephen Curtis, Jeffrey Goldsmith et al.
doi:10.1038/ncb2912

Errata

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Erratum: Plasma membrane translocation of trimerized MLKL protein is required for TNF-induced necroptosis   p200
Zhenyu Cai, Siriporn Jitkaew, Jie Zhao, Hsueh-Cheng Chiang, Swati Choksi et al.
doi:10.1038/ncb2908

Erratum: Kidney structures differentiated from stem cells   p200
Benjamin D. Humphreys
doi:10.1038/ncb2911

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