Tuesday, June 6, 2017

Nature Structural & Molecular Biology Contents: 2017 Volume #24 pp 491 - 553

If you are unable to see the message below, click here to view.
Nature Structural & Molecular Biology


Advertisement
npj Molecular Phenomics is an online-only, open access journal that provides a forum for cutting-edge scientific advances in the emerging field of phenomics, the study of the physical and chemical characteristics of an individual in quantitative terms. Part of the Nature Partner Journals series, npj Molecular Phenomics is published in partnership with Fudan University.

The journal is now open for submissions. 

Find out more >>>
TABLE OF CONTENTS

June 2017 Volume 24, Issue 6

Meeting Report
News and Views
Perspective
Articles
Erratum
Corrigendum
Advertisement
 
Collection: On Growth and Form Centenary

Join Nature in celebrating the centenary of D'Arcy Wentworth Thompson's seminal publication "On Growth and Form". We present an online collection of research and comment reflecting the diversity of explorative activity across the physical and biological sciences over the past 100 years. 

Access the On Growth and Form Centenary Collection


Subscribe
 
Facebook
 
RSS
 
Recommend to library
 
Twitter
 

Advertisement
Special offer! Recruit for less this summer! 

10% discount on our Enhanced job posting package 

20% discount on our Premium job posting package

Be displayed alongside relevant content across nature.com reaching a potential audience of 10.8 million users.*

Post a job now.

* Publisher data 2016

Offer ends June 19, 2017
 
Advertisement
Nature Reviews Microbiology: Collection on Antimicrobial Resistance 

This collection of articles from several Nature journals describes how antimicrobial resistance emerges and details discovery strategies for urgently needed new antimicrobials. 

Access this collection free online for six months

Produced with support from 
Merck & Co., Inc., Kenilworth, NJ, USA
 

Meeting Report

Top

Gathering by the Red Sea highlights links between environment and epigenetics   pp491 - 493
Mo Li, Emiliana Borrelli, Pierre J Magistretti, Juan Carlos Izpisua Belmonte, Paolo Sassone-Corsi et al.
doi:10.1038/nsmb.3422
The number of conferences on epigenetics has been increasing in the past decade, underscoring the impact of the field on a variety of areas in biology and medicine. However, the mechanistic role of the epigenome in adaptation and inheritance, and how the environment may impinge on epigenetic control, are topics of growing debate. Those themes were the focus of the inaugural international King Abdullah University of Science and Technology (KAUST) Research Conference on Environmental Epigenetics in Saudi Arabia, where more than 100 participants from 19 countries enjoyed vibrant scientific discussions and a pleasant February breeze from the Red Sea.

News and Views

Top

Promoter interactions direct chromatin folding in embryonic stem cells   pp494 - 495
Swastika Sanyal, Lucia Molnarova and Juraj Gregan
doi:10.1038/nsmb.3421
The spatial organization of the genome profoundly influences how genes are regulated in normal development or dysregulated in disease. A new study of the murine HoxB locus illustrates how promoter interactions direct higher-order chromatin folding.

See also: Article by Barbieri et al.

Distinct mechanisms obviate the potentially toxic effects of inverted-repeat Alu elements on cellular RNA metabolism   pp496 - 498
Reyad A Elbarbary and Lynne E Maquat
doi:10.1038/nsmb.3416
Two new studies show that RNA-binding proteins can mediate distinct and beneficial effects to cells by binding to the extensive double-stranded RNA (dsRNA) structures of inverted-repeat Alu elements (IRAlus). One study reports stress-induced export of the 110-kDa isoform of the adenosine deaminase acting on RNA 1 protein (ADAR1p110) to the cytoplasm, where it binds IRAlus so as to protect many mRNAs encoding anti-apoptotic proteins from degradation. The other study demonstrates that binding of the nuclear helicase DHX9 to IRAlus embedded within RNAs minimizes defects in RNA processing.

See also: Article by Sakurai et al.

A glimpse into chromatin remodeling   pp498 - 500
Dale B Wigley and Gregory D Bowman
doi:10.1038/nsmb.3415
Chromatin remodelers are ATP-driven enzymes that can slide nucleosomes along DNA. Chen and colleagues present a tantalizing ~4-A view of the SWI/SNF ATPase motor bound to the nucleosome, which offers novel structural clues into the remodeling process.

Frozen in action: cryo-EM structure of a GPCR-G-protein complex   pp500 - 502
Mithu Baidya, Hemlata Dwivedi and Arun K Shukla
doi:10.1038/nsmb.3418
Interaction with heterotrimeric G proteins is a hallmark of G-protein-coupled receptor (GPCR) family members, and it is the key step for a diverse range of cell-signaling cascades. A recent cryo-EM structure of the human calcitonin receptor (CTR) in complex with a G-protein heterotrimer reveals novel insights into receptor-G-protein coupling.

RNA base-pairing drives phase transitions   p502
Anke Sparmann
doi:10.1038/nsmb.3425

Structural & Molecular Biology
JOBS of the week
Post-doctoral Positions in Skeletal muscle Stem Cells and molecular medicine
Biology of the neuromuscular system Team IMRB U955-E10
POSTDOC in Cardiopulmonary Molecular Biology
Hannover Medical School (MHH)
A Postdoctoral Research Fellow position is available in the laboratory of Dr. Karen Mann, Department of Molecular Oncology and Cancer Biology and Evolution Program
Moffitt Cancer Center
Director for the Molecular Oncology Programme
Spanish National Research Centre (CNIO)
Molecular Geneticist / Computational Biologist
Deep Genomics
More Science jobs from
Structural & Molecular Biology
EVENT
The 3rd Conference on Advances in Biochemistry and Molecular Biology (CABMB 2017)
01.12.17
Sanya, China
More science events from

Perspective

Top

DNA N6-methyladenine in metazoans: functional epigenetic mark or bystander?   pp503 - 506
Guan-Zheng Luo and Chuan He
doi:10.1038/nsmb.3412
The DNA-adenine modification 6mA has recently been identified in metazoans. This Perspective summarizes the latest discoveries and suggests potential functional roles for 6mA in metazoan genomes.

Advertisement
nature.com webcasts

Springer Nature presents a custom webcast by Professor Aude Chapuis, MD on harnessing the therapeutic potential of adoptively transferred cells.

Register for FREE

Date: Thursday, June 22 2017
Time: 11AM PDT | 2PM EDT Register 

Sponsored by: 
10x Genomics
 

Articles

Top

Human CTP synthase filament structure reveals the active enzyme conformation   pp507 - 514
Eric M Lynch, Derrick R Hicks, Matthew Shepherd, James A Endrizzi, Allison Maker et al.
doi:10.1038/nsmb.3407
The human enzyme CTP synthase forms polymeric filaments with increased catalytic activity, in contrast to the inactive filaments formed by bacterial CTP synthase. Cryo-EM and crystallographic analyses explain the structural bases for those different behaviors.

Active and poised promoter states drive folding of the extended HoxB locus in mouse embryonic stem cells   pp515 - 524
Mariano Barbieri, Sheila Q Xie, Elena Torlai Triglia, Andrea M Chiariello, Simona Bianco et al.
doi:10.1038/nsmb.3402
Homotypic interactions between active and Polycomb-repressed promoters co-occurring in the same DNA fiber, rather than CTCF occupancy, explain the 3D HoxB folding pattern.

See also: News and Views by Sanyal et al.

The myosin mesa and the basis of hypercontractility caused by hypertrophic cardiomyopathy mutations   pp525 - 533
Suman Nag, Darshan V Trivedi, Saswata S Sarkar, Arjun S Adhikari, Margaret S Sunitha et al.
doi:10.1038/nsmb.3408
A working model for β-cardiac myosin in the sequestered state and binding assays reveal interactions between the myosin head and tail that are disrupted by mutations associated with hypertrophic cardiomyopathy.

ADAR1 controls apoptosis of stressed cells by inhibiting Staufen1-mediated mRNA decay   pp534 - 543
Masayuki Sakurai, Yusuke Shiromoto, Hiromitsu Ota, Chunzi Song, Andrew V Kossenkov et al.
doi:10.1038/nsmb.3403
In stressed cells, the ADAR1p110 isoform is phosphorylated and translocated from the nucleus to the cytoplasm, where it protects transcripts with 3′-UTR dsRNA structures from Staufen1-mediated decay, thus suppressing cellular apoptosis.

See also: News and Views by Elbarbary & Maquat

5-Formylcytosine does not change the global structure of DNA   pp544 - 552
Jack S Hardwick, Denis Ptchelkine, Afaf H El-Sagheer, Ian Tear, Daniel Singleton et al.
doi:10.1038/nsmb.3411
X-ray crystallography and NMR analysis demonstrate that, contrary to previous observations, fC does not significantly alter DNA structure, thus suggesting an alternative basis for recognition of fC-DNA by epigenome-modifying enzymes.

Advertisement
Special offer! Recruit for less this summer! 

10% discount on our Enhanced job posting package 

20% discount on our Premium job posting package

Be displayed alongside relevant content across nature.com reaching a potential audience of 10.8 million users.*

Post a job now.

* Publisher data 2016

Offer ends June 19, 2017
 

Erratum

Top

Erratum: Molecular basis of telomere dysfunction in human genetic diseases   p553
Grzegorz Sarek, Paulina Marzec, Pol Margalef and Simon J Boulton
doi:10.1038/nsmb0617-553a

Top

Corrigendum

Top

Corrigendum: Quaternary contact in the initial interaction of CD4 with the HIV-1 envelope trimer   p553
Qingbo Liu, Priyamvada Acharya, Michael A Dolan, Peng Zhang, Christina Guzzo et al.
doi:10.1038/nsmb0617-553b

nature events
Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. The contents of the Natureevents Directory are now live. The digital version is available here.
Find the latest scientific conferences, courses, meetings and symposia on natureevents.com. For event advertising opportunities across the Nature Publishing Group portfolio please contact natureevents@nature.com
More Nature Events

You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/myaccount
(You will need to log in to be recognised as a nature.com registrant)

For further technical assistance, please contact our registration department

For print subscription enquiries, please contact our subscription department

For other enquiries, please contact our customer feedback department

Springer Nature | One New York Plaza, Suite 4500 | New York | NY 10004-1562 | USA

Springer Nature's worldwide offices:
London - Paris - Munich - New Delhi - Tokyo - Melbourne
San Diego - San Francisco - Washington - New York - Boston

Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at The Campus, 4 Crinan Street, London, N1 9XW.

© 2017 Macmillan Publishers Limited, part of Springer Nature. All Rights Reserved.

Springer Nature

No comments: