Chakraborty D.,University Hospital and Medical |
Chakraborty D.,Max Planck Institute of Molecular Cell Biology and Genetics |
Kappei D.,University Hospital and Medical |
Kappei D.,Max Planck Institute of Molecular Cell Biology and Genetics |
And 17 more authors.
Nature Methods | Year: 2012
Whereas methods to comprehensively study cellular roles of protein-coding genes are available, techniques to systematically investigate long noncoding RNAs (lncRNAs), which have been implicated in diverse biological pathways, are limited. Here we report combined knockdown and localization analysis of noncoding RNAs (c-KLAN) that merges functional characterization and localization approaches to study lncRNAs. Using this technique we identified transcripts that regulate mouse embryonic stem cell identity. © 2012 Nature America, Inc. All rights reserved.
Donnelly S.K.,Cancer Research UK Research Institute |
Weisswange I.,Cancer Research UK Research Institute |
Weisswange I.,Eupheria Biotech GmbH |
Zettl M.,Cancer Research UK Research Institute |
And 2 more authors.
Current Biology | Year: 2013
Nck links phosphotyrosine-based signaling to Arp2/3-dependent actin polymerization during many different cellular processes as well as actin-based motility of enteropathogenic Escherichia coli (EPEC) [1, 2], vaccinia [3, 4], and other vertebrate poxviruses  by interacting with N-WASP/WASP [6, 7]. Nck also binds WASP-interacting protein (WIP) , which inhibits the ability of N-WASP to activate the Arp2/3 complex until it receives an appropriate signaling input [9, 10]. Using mouse embryonic fibroblasts (MEFs) lacking Nck, WIP, or N-WASP [3, 11, 12], we have investigated whether an interaction of Nck with both WIP and N-WASP is required for their recruitment to vaccinia during Arp2/3-dependent actin assembly. We find that WIP or its homolog WIRE is required for N-WASP recruitment and actin-based motility of the virus. WIP contains two Nck-binding sites and is recruited to the virus, bound to N-WASP, by interacting with the second SH3 domain of Nck. N-WASP also contains two Nck-binding sites, but its recruitment is dependent on its interaction with WIP rather than Nck. The first and third SH3 domains of Nck are not required to recruit the WIP:N-WASP complex but are essential to stimulate actin assembly. We have established that WIP acts as an essential link between Nck and N-WASP. Our observations provide important insights into the hierarchy and connections in one of the major cellular signaling networks stimulating Arp2/3 complex-dependent actin polymerization. © 2013 Elsevier Ltd.
Schmitt-Engel C.,University of Gottingen |
Schmitt-Engel C.,Friedrich - Alexander - University, Erlangen - Nuremberg |
Schultheis D.,Friedrich - Alexander - University, Erlangen - Nuremberg |
Schwirz J.,University of Gottingen |
And 32 more authors.
Nature Communications | Year: 2015
Genetic screens are powerful tools to identify the genes required for a given biological process. However, for technical reasons, comprehensive screens have been restricted to very few model organisms. Therefore, although deep sequencing is revealing the genes of ever more insect species, the functional studies predominantly focus on candidate genes previously identified in Drosophila, which is biasing research towards conserved gene functions. RNAi screens in other organisms promise to reduce this bias. Here we present the results of the iBeetle screen, a large-scale, unbiased RNAi screen in the red flour beetle, Tribolium castaneum, which identifies gene functions in embryonic and postembryonic development, physiology and cell biology. The utility of Tribolium as a screening platform is demonstrated by the identification of genes involved in insect epithelial adhesion. This work transcends the restrictions of the candidate gene approach and opens fields of research not accessible in Drosophila. © 2015 Macmillan Publishers Limited. All rights reserved.
Theis M.,TU Dresden |
Theis M.,Eupheria Biotech GmbH |
Paszkowski-Rogacz M.,TU Dresden |
Paszkowski-Rogacz M.,Eupheria Biotech GmbH |
And 4 more authors.
Journal of Biomolecular Screening | Year: 2015
Broad sequencing enterprises such as the FANTOM or ENCODE projects have substantially extended our knowledge of the human transcriptome. They have revealed that a large portion of genomic DNA is actively transcribed and have identified a plethora of novel transcripts. Many newly identified transcripts belong to the class of long noncoding RNAs (lncRNAs), which range from a few hundred bases to multiple kilobases in length and harbor no protein-coding potential. Although the biological activity of some lncRNAs is understood, the functions of most lncRNAs remain elusive. Tools that allow rapid and cost-effective access to functional data of lncRNAs are therefore essential. Here, we describe the construction and validation of an endoribonuclease-prepared siRNA (esiRNA) library designed to target 1779 individual human lncRNAs by RNA interference. We present a compendium of lncRNA expression data for 11 human cancer cell lines. Furthermore, we show that the resource is suitable for combined knockdown and localization analysis. We discuss challenges in sequence annotation of lncRNAs with respect to their often low and cell type-specific expression and specify esiRNAs that are suitable for targeting lncRNAs in commonly used human cell lines. © 2015 Society for Laboratory Automation and Screening.