Tuesday, June 23, 2015

Nature Reviews Molecular Cell Biology contents July 2015 Volume 16 Number 7 pp 389-449

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Nature Reviews Molecular Cell Biology


 
TABLE OF CONTENTS
 
July 2015 Volume 16 Number 7

Nature Reviews Molecular Cell Biology cover
Impact Factor 37.806 *
In this issue
Research Highlights
Reviews
Perspectives

Also this month
Article series:
Cell death and autophagy
Poster:
Stem cell states: naive to primed pluripotency
 Featured article:
Swiss army knives: non-canonical functions of nuclear Drosha and Dicer
Kaspar Burger & Monika Gullerova




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RESEARCH HIGHLIGHTS

Top

Autophagy: Selecting ER for eating
p389 | doi:10.1038/nrm4013
Two studies identify receptors that target the endoplasmic reticulum for autophagy-mediated degradation.
PDF


Circadian rhythms: Translating the clock
p390 | doi:10.1038/nrm4008
The major circadian transcription factor BMAL1 has independent circadian translational activity, which is regulated by the mTOR pathway kinase S6K1.
PDF


Mechanotransduction: Adhesion forces promote transcription
p390 | doi:10.1038/nrm4017
Mechanical forces activate YAP1 and β-catenin transcriptional activity in a cadherin-dependent manner.
PDF


JOURNAL CLUB
From hippos to yorkies in one pathway

p392 | doi:10.1038/nrm4011
Barry Thompson reminds us how Yorkie was discovered as the transcriptional coactivator downstream of Hippo signalling.
PDF


Unfolded protein response: Regulatory ribosomal ubiquitylation
p392 | doi:10.1038/nrm4016
The ubiquitylation of specific Lys residues of 40S ribosomal proteins is stimulated by the unfolded protein response to contribute to translational regulation.
PDF



IN BRIEF

RNA metabolism: Methyladenosine promotes translation | Splicing: Unmasking exitrons | Chromosomes: Finding the right size | Cell adhesion: Sticking three cells together | Techniques: microRNA switches to isolate specific cells | DNA damage response: Damage by Helicobacter pylori
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Molecular Cell Biology
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REVIEWS

Top
Article series: Cell death and autophagy
p53 in survival, death and metabolic health: a lifeguard with a licence to kill
Flore Kruiswijk, Christiaan F. Labuschagne & Karen H. Vousden
p393 | doi:10.1038/nrm4007
The function of p53 as a tumour suppressor has been attributed to its ability to promote cell death or permanently inhibit cell proliferation. However, p53 can also contribute to cell survival by regulating various metabolic pathways to allow cells to adapt to mild metabolic stresses.
Abstract | Full Text | PDF


Specifying and protecting germ cell fate
Susan Strome & Dustin Updike
p406 | doi:10.1038/nrm4009
Recent studies in different species have increased our understanding of the factors and molecular mechanisms that underlie the specification of germ cells, which are the specialized cells that generate gametes. Moreover, studies are elucidating how these cells ensure that only germline-appropriate transcripts are translated to protect germ cell identity.
Abstract | Full Text | PDF


Swiss army knives: non-canonical functions of nuclear Drosha and Dicer
Kaspar Burger & Monika Gullerova
p417 | doi:10.1038/nrm3994
Recent studies have revealed that the RNase III enzymes Drosha and Dicer (including newly discovered Dicer isoforms) have non-canonical nuclear RNAi functions in various organisms. These include the regulation of transcription initiation and termination, and the processing of various RNA species.
Abstract | Full Text | PDF | Supplementary information


Control of mammalian gene expression by selective mRNA export
Vihandha O. Wickramasinghe & Ronald A. Laskey
p431 | doi:10.1038/nrm4010
Recent studies have shown that nuclear export of mRNAs, which is a crucial step in the regulation of gene expression, can be selective in mammalian cells. Selective transport involves transcription-export complexes TREX and TREX-2 and controls biological processes such as DNA repair, haematopoiesis, proliferation and maintenance of pluripotency.
Abstract | Full Text | PDF



 
PERSPECTIVES

Top
ESSAY
Discovering centromere proteins: from cold white hands to the A, B, C of CENPs
William C. Earnshaw
p443 | doi:10.1038/nrm4001
William Earnshaw describes the events that led to the discovery and cloning of the first kinetochore proteins 30 years ago using autoimmune sera from patients with scleroderma-spectrum disease. He also discusses our current appreciation of the complexity of this remarkable structure.
Abstract | Full Text | PDF


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