Research Topics
| Ann E Ehrenhofer-MurraySummaryAffiliation: Max Planck Institute for Molecular Genetics Country: Germany Publications
| Collaborators
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Detail Information
Publications
Interactions within the mammalian DNA methyltransferase familyJean B Margot
Ludwig Maximilians University, Department of Biology II, Goethestr, 31, D 80336 Munich, Germany
BMC Mol Biol 4:7. 2003..Deletion analysis has revealed that a large part of the N-terminal domain is required for enzymatic activity...
Dependence of ORC silencing function on NatA-mediated Nalpha acetylation in Saccharomyces cerevisiaeAntje Geissenhöner
Otto Warburg Laboratorium, Max Planck Institut fur Molekulare Genetik, Ihnestr 73, D 14195 Berlin, Germany
Mol Cell Biol 24:10300-12. 2004..In summary, we propose a model by which N(alpha) acetylation is required for the binding of silencing factors to the N terminus of Orc1p and Sir3p to recruit heterochromatic factors and establish repression...
Chromatin dynamics at DNA replication, transcription and repairAnn E Ehrenhofer-Murray
Otto Warburg Laboratories, Max Planck Institute of Molecular Genetics, Berlin, Germany
Eur J Biochem 271:2335-49. 2004..This review will summarize the current knowledge of how chromatin remodeling and histone modifying complexes cooperate to break and remake chromatin during nuclear processes on the DNA template...
Control of replication initiation and heterochromatin formation in Saccharomyces cerevisiae by a regulator of meiotic gene expressionHorst Irlbacher
Otto Warburg Laboratorium and Department for Computational Molecular Biology, Max Planck Institut fur Molekulare Genetik, D 14195 Berlin, Germany
Genes Dev 19:1811-22. 2005..Full initiation activity of these origins required Sum1, and their origin activity was decreased upon removal of the Sum1-binding site. Thus, Sum1 constitutes a novel global regulator of replication initiation in yeast...
Nuclear import of the histone acetyltransferase complex SAS-I in Saccharomyces cerevisiaeSigrid Schaper
Otto Warburg Laboratories, Max Planck Institute of Molecular Genetics, Ihnestrasse 73, 14195 Berlin, Germany
J Cell Sci 118:1473-84. 2005..A database search based on the aligned consensus sequence revealed potential new import substrates of the Kap123p and Pse1p nuclear import pathways, which are connected to chromatin function...
Genome-wide H4 K16 acetylation by SAS-I is deposited independently of transcription and histone exchangeFranziska Heise
Zentrum für Medizinische Biotechnologie, Abteilung Genetik, Universitat Duisburg Essen, Essen, Germany
Nucleic Acids Res 40:65-74. 2012....
SIR-dependent repression of non-telomeric genes in Saccharomyces cerevisiae?Uta Marchfelder
Otto Warburg Laboratories, Max Planck Institut fur Molekulare Genetik, D 14195 Berlin, Germany
Yeast 20:797-801. 2003..However, we were unable to verify their SIR-dependent regulation, which suggests that SIR-mediated repression may be restricted to the known repressed regions...
The effect of micrococcal nuclease digestion on nucleosome positioning dataHo Ryun Chung
Department of Computational Molecular Biology, MPI für Molekulare Genetik, Berlin, Germany
PLoS ONE 5:e15754. 2010..More generally, our results show that data generated after MNase digestion of chromatin requires a matched control experiment in order to determine nucleosome positions...
A novel yeast silencer. the 2mu origin of Saccharomyces cerevisiae has HST3-, MIG1- and SIR-dependent silencing activityArnold Grünweller
Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany
Genetics 162:59-71. 2002..Also, Hst3 regulated the repression of the flipase gene, although this was likely an indirect effect of HST3 on FLP1 expression...
A role for the Saccharomyces cerevisiae RENT complex protein Net1 in HMR silencingDaniela Kasulke
Max-Planck-Institute for Molecular Genetics, 14195 Berlin, Germany
Genetics 161:1411-23. 2002..In contrast, our data suggested that net1-1 acted indirectly in HMR silencing by releasing Sir2 from the nucleolus, thus shifting the internal competition for Sir2 from the silenced loci toward HMR...
