Table of contents
May 2008 Vol 9 No 5
From the editors
p319 | doi:10.1038/nrg2376
Research Highlights
Complex traits: A wider view of networks | PDF (197 KB)
p321 | doi:10.1038/nrg2367
Human disease: A two-pronged model of polyglutamine disease | PDF (177 KB)
p322 | doi:10.1038/nrg2366
In the news
Lifting the smoke screen | PDF (127 KB)
p322 | doi:10.1038/nrg2371
Gene regulation: Repositioning tunes expression | PDF (139 KB)
p322 | doi:10.1038/nrg2377
In brief
Network biology | Statistical genetics | Evo–devo | Population genetics | PDF (128 KB)
p323 | doi:10.1038/nrg2372
In brief
RNA world | Gene regulation | Genomics | PDF (97 KB)
p324 | doi:10.1038/nrg2373
Evolution: Scrutinizing mammalian reproductive inventions | PDF (117 KB)
p324 | doi:10.1038/nrg2375
Ethics watch
LCN DNA: proof beyond reasonable doubt? | PDF (208 KB)
p325 | doi:10.1038/nrg2362
See also: Correspondence by Gill | Correspondence by McCartney
Human disease: Rare but rich pickings | PDF (246 KB)
p326 | doi:10.1038/nrg2370
Epigenetics: Pioneering the path from methylation to transcription | PDF (138 KB)
p326 | doi:10.1038/nrg2378
An Interview With...
Philip Beachy | PDF (139 KB)
p327 | doi:10.1038/nrg2368
Reviews
Genetic programming of liver and pancreas progenitors: lessons for stem-cell differentiation
Kenneth S. Zaret
p329 | doi:10.1038/nrg2318
Newly specified hepatic and pancreatic progenitors, which originate from common endodermal domains, are able to reverse their course and develop into gut progenitors. Understanding what underlies such programming reversal and intrinsic regenerative capacities should illuminate the basis of cellular plasticity and facilitate targeted programming of stem cells.
Advances in autism genetics: on the threshold of a new neurobiology
Brett S. Abrahams & Daniel H. Geschwind
p341 | doi:10.1038/nrg2346
The highly heterogeneous nature of autism has made this syndrome difficult to dissect genetically. Recent work has highlighted the importance of de novo and inherited copy number variation as well as common genetic risk variants in defining potential biological mechanisms of disease.
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
Mark I. McCarthy, Gonçalo R. Abecasis, Lon R. Cardon, David B. Goldstein, Julian Little, John P. A. Ioannidis & Joel N. Hirschhorn
p356 | doi:10.1038/nrg2344
Genome-wide association studies have led to an improved understanding of the genetic basis of common diseases. Following the first wave of such studies, this Review takes a critical look at progress so far and considers how future studies can be optimized.
Segmental patterning of the vertebrate embryonic axis
Mary-Lee Dequéant & Olivier Pourquié
p370 | doi:10.1038/nrg2320
Established during embryogenesis, vertebrate segmentation is most conspicuous at the level of the periodic arrangement of vertebrae in the spine. Since the identification of the segmentation clock, which is a travelling oscillator, the generation of segmental pattern in the presomitic mesoderm has been a particular focus of attention.
Coordination of gene expression between organellar and nuclear genomes
Jesse D. Woodson & Joanne Chory
p383 | doi:10.1038/nrg2348
Tight coordination of gene expression between the nucleus and genome-containing organelles (mitochondria and chloroplasts), and between organelles themselves, is essential to the survival of a eukaryotic cell. This article reviews our current understanding of the mechanisms behind this multidirectional signalling.
Perspectives
Opinion
Transposable elements and the evolution of regulatory networks
Cédric Feschotte
p397 | doi:10.1038/nrg2337
How did the complex regulatory networks that control eukaryotic gene expression evolve? This article explores evidence that transposable elements played an important part by providing the cis and trans components of these networks.
Science and society
From genetic privacy to open consent
Jeantine E. Lunshof, Ruth Chadwick, Daniel B. Vorhaus & George M. Church
p406 | doi:10.1038/nrg2360
The unprecedented amount of data in biomedical sciences is putting the well-known ethical issues such as privacy, confidentiality and consent for research under pressure. These authors propose that an open-consent framework, as implemented in the Personal Genome Project, might help avoid the constraints that are inherent in the current concepts of genetic privacy.
Correspondence
Correspondence: A universal classification of eukaryotic transposable elements implemented in Repbase
Vladimir V. Kapitonov & Jerzy Jurka
p411 | doi:10.1038/nrg2165-c1
Author Reply: A universal classification of eukaryotic transposable elements implemented in Repbase
Thomas Wicker, François Sabot, Aurélie Hua-Van, Jeffrey L. Bennetzen, Pierre Capy, Boulos Chalhoub, Andrew Flavell, Philippe Leroy, Michele Morgante, Olivier Panaud, Etienne Paux, Phillip SanMiguel & Alan H. Schulman
p414 | doi:10.1038/nrg2165-c2

