News & Views |
Featured
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Brief Communications Arising |
Singh et al. reply
- Sanjay K. Singh
- , Mohamedi N. Kagalwala
- & Sadhan Majumder
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Brief Communications Arising |
Can controversies be put to REST?
- Helle F. Jørgensen
- & Amanda G. Fisher
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Article |
Neurotrophin receptors TrkA and TrkC cause neuronal death whereas TrkB does not
Neurons of the peripheral nervous system need survival factors to prevent their death during development. Most in the central nervous system do not. Why are peripheral neurons so needy? Here it is shown that the neurotrophin receptors TrkA and TrkC, expressed at high levels by many peripheral nervous system neurons, behave as dependence receptors: they instruct neurons to die if there is no ligand around. By contrast, TrkB, expressed mainly in the central nervous system, does not signal death in the absence of ligand.
- Vassiliki Nikoletopoulou
- , Heiko Lickert
- & Yves-Alain Barde
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Article |
Mediator and cohesin connect gene expression and chromatin architecture
Gene activation may involve the formation of a DNA loop that connects enhancer-bound transcription factors with the transcription apparatus at the core promoter. But this process is not well understood. Here, two proteins, mediator and cohesin, are shown to connect the enhancers and core promoters of active genes in embryonic stem cells. These proteins seem to generate cell-type-specific DNA loops linked to the gene expression program of each cell.
- Michael H. Kagey
- , Jamie J. Newman
- & Richard A. Young
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Letter |
Production of p53 gene knockout rats by homologous recombination in embryonic stem cells
The rat is a animal model widely used for studying human physiology and disease, but functional genomics and genetic research have been stifled by the limited availability of gene targeting tools. These authors have established gene targeting by homologous recombination in rat embryonic stem cells, and have generated p53 gene knockout rats for the first time.
- Chang Tong
- , Ping Li
- & Qi-Long Ying
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News |
Diseased cells fail to win approval
Consent form signed by clinic's donors falls short of 'high ethical standards' set by the NIH.
- Meredith Wadman
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News |
Gene flaw found in induced stem cells
Key difference between reprogrammed adult mouse cells and embryonic stem cells discovered.
- Elie Dolgin
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Article |
Zscan4 regulates telomere elongation and genomic stability in ES cells
Zscan4 is shown to be involved in maintaining telomeres in embryonic stem (ES) cells. Only 5% of ES cells express Zscan4 at a given time, but nearly all ES cells activate Zscan4 at least once within nine passages. The transient Zscan4-positive state is associated with rapid telomere extension by telomere recombination and upregulation of meiosis–specific homologous recombination genes. Knocking down Zscan4 shortens telomeres, increases karyotype abnormalities and spontaneous sister chromatid exchange, and slows down cell proliferation until reaching crisis by eight passages.
- Michal Zalzman
- , Geppino Falco
- & Minoru S. H. Ko
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Letter |
Chromatin signature of embryonic pluripotency is established during genome activation
To study the changes in chromatin structure that accompany zygotic genome activation and pluripotency during the maternal–zygotic transition (MZT), the genomic locations of histone H3 modifications and RNA polymerase II have been mapped during this transition in zebrafish embryos. H3 lysine 27 trimethylation and H3 lysine 4 trimethylation are only detected after MZT; evidence is provided that the bivalent chromatin domains found in cultured embryonic stem cells also exist in embryos.
- Nadine L. Vastenhouw
- , Yong Zhang
- & Alexander F. Schier
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News |
NIH may allow stem-cell lines from younger embryos
Lines derived from pre-blastocyst stage embryos could be eligible for agency funding.
- Meredith Wadman
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Letter |
Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET
Endogenous retroviruses (ERVs) are widely dispersed in mammalian genomes, and are silenced in somatic cells by DNA methylation. Here, an ERV silencing pathway independent of DNA methylation is shown to operate in embryonic stem cells. The pathway involves the histone H3K9 methyltransferase ESET and might be important for ERV silencing during the stages in embryogenesis when DNA methylation is reprogrammed.
- Toshiyuki Matsui
- , Danny Leung
- & Yoichi Shinkai
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Correspondence |
Italy's stem-cell challenge gaining momentum
- Elena Cattaneo
- , Elisabetta Cerbai
- & Silvia Garagna
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News & Views |
Big roles for small RNAs
Embryonic stem cells can create copies of themselves, but can also mature into almost any type of cell in the body. Tiny gene regulators called microRNAs are now shown to have a role in directing these properties.
- Frank J. Slack
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Research Highlights |
Regenerative biology: New nerve cells connect
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News |
Stem-cell line given the nod
NIH moves to approve cells in limbo after rule change.
- Brendan Borrell
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Letter |
KAP1 controls endogenous retroviruses in embryonic stem cells
Much of the mammalian genome is derived from retroelements, a significant proportion of which are endogenous retroviruses (ERVs). ERVs are transcriptionally silenced during early embryogenesis by histone and DNA methylation, but the initiators of this process are largely unknown. Here, deletion of KAP1 is shown to lead to a marked upregulation of a range of ERVs in mouse embryonic stem cells and in early embryos.
- Helen M. Rowe
- , Johan Jakobsson
- & Didier Trono
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Article |
Opposing microRNA families regulate self-renewal in mouse embryonic stem cells
The differentiation of an embryonic stem cell (ESC) requires both suppression of the self-renewal process and activation of the specific differentiation pathway. The let-7 family of microRNAs (miRNAs) are now shown to suppress the self-renewal program in cells that are normally unable to silence this program, whereas introduction of ESC cell cycle regulating miRNAs blocks the action of let-7. Thus, the interplay between these two groups of miRNAs dictates cell fate.
- Collin Melton
- , Robert L. Judson
- & Robert Blelloch