<description/> <link>http://www.nature.com/emboj/current_issue/</link> <dc:publisher>Nature Publishing Group</dc:publisher> <dc:language>en</dc:language> <dc:rights>© 2009 Nature Publishing Group</dc:rights> <prism:publicationName/> <prism:issn>0261-4189</prism:issn> <prism:eIssn>1460-2075</prism:eIssn> <prism:copyright>© 2009 Nature Publishing Group</prism:copyright> <prism:rightsAgent>permissions@nature.com</prism:rightsAgent> <image rdf:resource="http://www.nature.com/includes/rj_globnavimages/emboj_logo.gif"/> <items> <rdf:Seq> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.250"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.261"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.251"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.253"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.238"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.256"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.260"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.259"/> <rdf:li rdf:resource="http://dx.doi.org/10.1038/emboj.2008.254"/> </rdf:Seq> </items> </channel> <image rdf:about="http://www.nature.com/includes/rj_globnavimages/emboj_logo.gif"> <title/> <url>http://www.nature.com/includes/rj_globnavimages/emboj_logo.gif</url> <link>http://www.nature.com/emboj/</link> </image> <item rdf:about="http://dx.doi.org/10.1038/emboj.2008.250"> <title>The EMBO Journal 2009: new initiatives http://dx.doi.org/10.1038/emboj.2008.250 The EMBO Journal 2009: new initiatives

28, 1 (2009). doi:10.1038/emboj.2008.250

Author: Pernille Rørth

]]> The EMBO Journal 2009: new initiatives Pernille Rørth doi:10.1038/emboj.2008.250 28, 1 (2009) 2008-12-04 2008-12-04 28 1 Editorial 1 3 TRPCs, GPCRs and the Bayliss effect http://dx.doi.org/10.1038/emboj.2008.261 An increase in pressure inside most small arteries unexpectedly results in a vasoconstriction. This phenomenon, known as the Bayliss effect, involves the stretch-induced activation of non-selective cation channels in the vascular smooth muscle cells. Recent work by Mederos y Schnitzler et al. now demonstrates TRPCs, GPCRs and the Bayliss effect

28, 4 (2009). doi:10.1038/emboj.2008.261

Authors: Thomas Voets & Bernd Nilius

An increase in pressure inside most small arteries unexpectedly results in a vasoconstriction. This phenomenon, known as the Bayliss effect, involves the stretch-induced activation of non-selective cation channels in the vascular smooth muscle cells. Recent work by Mederos y Schnitzler et al. now demonstrates

]]>
TRPCs, GPCRs and the Bayliss effect Thomas Voets Bernd Nilius doi:10.1038/emboj.2008.261 28, 4 (2009) 28 1 Have you seen ...? 4 5 One for all? A viral protein supplants the mRNA cap-binding complex http://dx.doi.org/10.1038/emboj.2008.251 Modulation of the host cell's translational machinery is a crucial part of viral infection strategies. Well-characterised mechanisms that aid viruses in manipulating translational activity include, for example, internal ribosomal entry sites, which allow viral RNA translation in the absence of some or many of the One for all? A viral protein supplants the mRNA cap-binding complex

28, 6 (2009). doi:10.1038/emboj.2008.251

Author: Tobias von der Haar

Modulation of the host cell's translational machinery is a crucial part of viral infection strategies. Well-characterised mechanisms that aid viruses in manipulating translational activity include, for example, internal ribosomal entry sites, which allow viral RNA translation in the absence of some or many of the

]]>
One for all? A viral protein supplants the mRNA cap-binding complex Tobias von der Haar doi:10.1038/emboj.2008.251 28, 6 (2009) 28 1 Have you seen ...? 6 7
Cancer induction by restriction of oncogene expression to the stem cell compartment http://dx.doi.org/10.1038/emboj.2008.253 In human cancers, all cancerous cells carry the oncogenic genetic lesions. However, to elucidate whether cancer is a stem cell-driven tissue, we have developed a strategy to limit oncogene expression to the stem cell compartment in a transgenic mouse setting. Here, we focus on the Cancer induction by restriction of oncogene expression to the stem cell compartment

28, 8 (2009). doi:10.1038/emboj.2008.253

Authors: María Pérez-Caro, César Cobaleda, Inés González-Herrero, Carolina Vicente-Dueñas, Camino Bermejo-Rodríguez, Margarita Sánchez-Beato, Alberto Orfao, Belén Pintado, Teresa Flores, Manuel Sánchez-Martín, Rafael Jiménez, Miguel A Piris & Isidro Sánchez-García

In human cancers, all cancerous cells carry the oncogenic genetic lesions. However, to elucidate whether cancer is a stem cell-driven tissue, we have developed a strategy to limit oncogene expression to the stem cell compartment in a transgenic mouse setting. Here, we focus on the

]]>
Cancer induction by restriction of oncogene expression to the stem cell compartment María Pérez-Caro César Cobaleda Inés González-Herrero Carolina Vicente-Dueñas Camino Bermejo-Rodríguez Margarita Sánchez-Beato Alberto Orfao Belén Pintado Teresa Flores Manuel Sánchez-Martín Rafael Jiménez Miguel A Piris Isidro Sánchez-García doi:10.1038/emboj.2008.253 28, 8 (2009) 2008-11-27 2008-11-27 28 1 Article 8 20
PTEN regulation by Akt–EGR1–ARF–PTEN axis http://dx.doi.org/10.1038/emboj.2008.238 The PTEN tumour suppressor gene is induced by the early growth response 1 (EGR1) transcription factor, which also transactivates p53, p73, and p300/CBP as well as other proapoptotic and anti-cancer genes. Here, we describe a novel Akt–EGR1–alternate reading frame (ARF)–PTEN axis, in which PTEN activation PTEN regulation by Akt–EGR1–ARF–PTEN axis

28, 21 (2009). doi:10.1038/emboj.2008.238

Authors: Jianxiu Yu, Sharon S Zhang, Kan Saito, Scott Williams, Yutaka Arimura, Yuliang Ma, Yuehai Ke, Veronique Baron, Dan Mercola, Gen-Sheng Feng, Eileen Adamson & Tomas Mustelin

The PTEN tumour suppressor gene is induced by the early growth response 1 (EGR1) transcription factor, which also transactivates p53, p73, and p300/CBP as well as other proapoptotic and anti-cancer genes. Here, we describe a novel Akt–EGR1–alternate reading frame (ARF)–PTEN axis, in which PTEN activation

]]>
PTEN regulation by Akt–EGR1–ARF–PTEN axis Jianxiu Yu Sharon S Zhang Kan Saito Scott Williams Yutaka Arimura Yuliang Ma Yuehai Ke Veronique Baron Dan Mercola Gen-Sheng Feng Eileen Adamson Tomas Mustelin doi:10.1038/emboj.2008.238 28, 21 (2009) 2008-12-04 2008-12-04 28 1 Article 21 33
A coordinated phosphorylation cascade initiated by p38MAPK/MSK1 directs RARα to target promoters http://dx.doi.org/10.1038/emboj.2008.256 The nuclear retinoic acid (RA) receptor alpha (RARα) is a transcriptional transregulator that controls the expression of specific gene subsets through binding at response elements and dynamic interactions with coregulators, which are coordinated by the ligand. Here, we highlighted a novel paradigm in which the A coordinated phosphorylation cascade initiated by p38MAPK/MSK1 directs RARα to target promoters

28, 34 (2009). doi:10.1038/emboj.2008.256

Authors: Nathalie Bruck, Dominique Vitoux, Christine Ferry, Vanessa Duong, Annie Bauer, Hughes de Thé & Cécile Rochette-Egly

The nuclear retinoic acid (RA) receptor alpha (RARα) is a transcriptional transregulator that controls the expression of specific gene subsets through binding at response elements and dynamic interactions with coregulators, which are coordinated by the ligand. Here, we highlighted a novel paradigm in which the

]]>
A coordinated phosphorylation cascade initiated by p38MAPK/MSK1 directs RARα to target promoters Nathalie Bruck Dominique Vitoux Christine Ferry Vanessa Duong Annie Bauer Hughes de Thé Cécile Rochette-Egly doi:10.1038/emboj.2008.256 28, 34 (2009) 2008-12-11 2008-12-11 28 1 Article 34 47
A stepwise pathway for biogenesis of 24-nt secondary siRNAs and spreading of DNA methylation http://dx.doi.org/10.1038/emboj.2008.260 We used a transgene system to study spreading of RNA-directed DNA methylation (RdDM) during transcriptional gene silencing in Arabidopsis thaliana. Forward and reverse genetics approaches using this system delineated a stepwise pathway for the biogenesis of secondary siRNAs and unidirectional spreading of methylation from A stepwise pathway for biogenesis of 24-nt secondary siRNAs and spreading of DNA methylation

28, 48 (2009). doi:10.1038/emboj.2008.260

Authors: Lucia Daxinger, Tatsuo Kanno, Etienne Bucher, Johannes van der Winden, Ulf Naumann, Antonius J M Matzke & Marjori Matzke

We used a transgene system to study spreading of RNA-directed DNA methylation (RdDM) during transcriptional gene silencing in Arabidopsis thaliana. Forward and reverse genetics approaches using this system delineated a stepwise pathway for the biogenesis of secondary siRNAs and unidirectional spreading of methylation from

]]>
A stepwise pathway for biogenesis of 24-nt secondary siRNAs and spreading of DNA methylation Lucia Daxinger Tatsuo Kanno Etienne Bucher Johannes van der Winden Ulf Naumann Antonius J M Matzke Marjori Matzke doi:10.1038/emboj.2008.260 28, 48 (2009) 2008-12-11 2008-12-11 28 1 Article 48 57
General RNA-binding proteins have a function in poly(A)-binding protein-dependent translation http://dx.doi.org/10.1038/emboj.2008.259 The interaction between the poly(A)-binding protein (PABP) and eukaryotic translational initiation factor 4G (eIF4G), which brings about circularization of the mRNA, stimulates translation. General RNA-binding proteins affect translation, but their role in mRNA circularization has not been studied before. Here, we demonstrate that the major General RNA-binding proteins have a function in poly(A)-binding protein-dependent translation

28, 58 (2009). doi:10.1038/emboj.2008.259

Authors: Yuri V Svitkin, Valentina M Evdokimova, Ann Brasey, Tatyana V Pestova, Daniel Fantus, Akiko Yanagiya, Hiroaki Imataka, Maxim A Skabkin, Lev P Ovchinnikov, William C Merrick & Nahum Sonenberg

The interaction between the poly(A)-binding protein (PABP) and eukaryotic translational initiation factor 4G (eIF4G), which brings about circularization of the mRNA, stimulates translation. General RNA-binding proteins affect translation, but their role in mRNA circularization has not been studied before. Here, we demonstrate that the major

]]>
General RNA-binding proteins have a function in poly(A)-binding protein-dependent translation Yuri V Svitkin Valentina M Evdokimova Ann Brasey Tatyana V Pestova Daniel Fantus Akiko Yanagiya Hiroaki Imataka Maxim A Skabkin Lev P Ovchinnikov William C Merrick Nahum Sonenberg doi:10.1038/emboj.2008.259 28, 58 (2009) 2008-12-11 2008-12-11 28 1 Article 58 68
Identification, structure, and functional requirement of the Mediator submodule Med7N/31 http://dx.doi.org/10.1038/emboj.2008.254 Mediator is a modular multiprotein complex required for regulated transcription by RNA polymerase (Pol) II. Here, we show that the middle module of the Mediator core contains a submodule of unique structure and function that comprises the N-terminal part of subunit Med7 (Med7N) and the Identification, structure, and functional requirement of the Mediator submodule Med7N/31

28, 69 (2009). doi:10.1038/emboj.2008.254

Authors: Tobias Koschubs, Martin Seizl, Laurent Larivière, Fabian Kurth, Sonja Baumli, Dietmar E Martin & Patrick Cramer

Mediator is a modular multiprotein complex required for regulated transcription by RNA polymerase (Pol) II. Here, we show that the middle module of the Mediator core contains a submodule of unique structure and function that comprises the N-terminal part of subunit Med7 (Med7N) and the

]]>
Identification, structure, and functional requirement of the Mediator submodule Med7N/31 Tobias Koschubs Martin Seizl Laurent Larivière Fabian Kurth Sonja Baumli Dietmar E Martin Patrick Cramer doi:10.1038/emboj.2008.254 28, 69 (2009) 2008-12-04 2008-12-04 28 1 Article 69 80