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2016/03/22

Nature Reviews Molecular Cell Biology contents January 2016 Volume 17 Number 4 pp 201-262

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Nature Reviews Molecular Cell Biology


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This special Focus highlights the unprecedented insights gained into the regulatory mechanisms underlying nuclear reprogramming, pluripotency and cell identity, and looks at the progress and challenges in using embryonic stem (ES) cells and iPSCs for therapeutic applications. Available free online

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TABLE OF CONTENTS
 
April 2016 Volume 17 Number 4
Nature Reviews Molecular Cell Biology cover
Impact Factor 37.806 *
In this issue
Research Highlights
Progress
Reviews
Perspectives

Also this month
 Featured article:
Mitonuclear communication in homeostasis and stress
Pedro M. Quirós, Adrienne Mottis & Johan Auwerx
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RESEARCH HIGHLIGHTSTop

RNA: Expanding the mRNA epitranscriptome
p201 | doi:10.1038/nrm.2016.35
Two new studies report the identification and comprehensive analysis of the m1A mRNA modification, showing that this mark is enriched at the 5' UTRs of mRNAs and might have a functional role in promoting translation of methylated transcripts.
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Cancer biology: TGFβ and EMT as double agents
p202 | doi:10.1038/nrm.2016.26
TGFβ signalling induces EMT and elicits apoptosis by switching SOX4 from acting as a tumour promoter to a tumour suppressor.
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Gene expression: Buffering newly replicated DNA
p202 | doi:10.1038/nrm.2016.34
Acetylation of H3K56 suppresses the transcription of newly replicated DNA during S phase to buffer changes in gene expression.
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JOURNAL CLUB
Eukaryotic antisense ahead of its time

p204 | doi:10.1038/nrm.2016.1
Lynne Maquat reminds us that almost 20 years before the discovery of microRNAs, an antisense regulatory RNA was identified in embryonic chick muscle cells.
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Metabolism: Restoring brown fat commitment
p204 | doi:10.1038/nrm.2016.28
The role of DICER1-miR-328-BACE1 signalling in brown adipose tissue differentiation and function.
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IN BRIEF

Cell adhesion: Autophagy consumes integrin junctions | Mechanisms of disease: Benefits of oxygen limitation | Non-coding RNA: 7SK dampens transcription at super-enhancers
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Molecular Cell Biology
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PROGRESSTop
The biogenesis and emerging roles of circular RNAs
Ling-Ling Chen
p205 | doi:10.1038/nrm.2015.32
Circular RNAs (circRNAs) are produced from precursor RNA back-splicing. Recent findings reveal the complexity of the biogenesis of circRNAs and their cell type-specific expression. They also show that circRNAs can shape eukaryotic transcriptomes by sequestering microRNAs and by regulating transcription and interfering with splicing.
Abstract | Full Text | PDF
 
REVIEWSTop
Mitonuclear communication in homeostasis and stress
Pedro M. Quirós, Adrienne Mottis & Johan Auwerx
p213 | doi:10.1038/nrm.2016.23
As most mitochondrial proteins are encoded in the nucleus, mitochondrial activity requires efficient communication between the nuclear and mitochondrial genomes. This is mediated by nucleus-to-mitochondria (anterograde), mitochondria-to-nucleus (retrograde) and mitonuclear feedback signalling, as well as the integrated stress response and extracellular communication, which regulate homeostasis and, consequently, healthspan and lifespan.
Abstract | Full Text | PDF
The regulation and functions of the nuclear RNA exosome complex
Cornelia Kilchert, Sina Wittmann & Lidia Vasiljeva
p227 | doi:10.1038/nrm.2015.15
The versatile RNA-degradation functions of the RNA exosome complex make it crucial for RNA biogenesis. It is now emerging that the nuclear exosome is a specific regulator of gene expression in different physiological processes, and that it has a role in transcription regulation and in maintaining genome stability.
Abstract | Full Text | PDF
Mechanisms of ephrin-Eph signalling in development, physiology and disease
Artur Kania & Rüdiger Klein
p240 | doi:10.1038/nrm.2015.16
Ephrin ligands and Eph receptor Tyr kinases are transmembrane proteins that elicit short-distance cell-cell signalling when they interact. As both Eph kinases and ephrins exist in various isoforms and function as receptors or ligands, this signalling evokes versatile responses, which regulate a plethora of morphogenetic and homeostatic processes.
Abstract | Full Text | PDF
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PERSPECTIVESTop
OPINION
Do short, frequent DNA sequence motifs mould the epigenome?
Timo Quante & Adrian Bird
p257 | doi:10.1038/nrm.2015.31
Quante and Bird propose that the epigenome is modulated by the recruitment of cell type-specific DNA-binding proteins to short, abundant sequence motifs. The regulation of gene expression may thus be simplified by tuning gene expression in multigene blocks.
Abstract | Full Text | PDF
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