Research Topics
| Mark PtashneSummaryAffiliation: Memorial Sloan-Kettering Cancer Center Country: USA Publications
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Detail Information
Publications
Activator control of nucleosome occupancy in activation and repression of transcriptionGene O Bryant
Molecular Biology Program, Sloan Kettering Institute, New York, New York, United States of America
PLoS Biol 6:2928-39. 2008..These findings were made possible by our nucleosome occupancy assay. The assay, we believe, will prove useful in studying other outstanding issues in the field...
Lambda's switch: lessons from a module swapMark Ptashne
Memorial Sloan Kettering Cancer Center, New York, New York 10021, USA
Curr Biol 16:R459-62. 2006..The resulting hybrid phage is viable, but a subtle phenotypic defect explains a puzzle concerning the workings of the switch...
On the use of the word 'epigenetic'Mark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA
Curr Biol 17:R233-6. 2007..Here I wish to probe our use of language in this way, and to show how such a discussion leads to some more general considerations concerning gene regulation...
On speaking, writing and inspirationMark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 595, New York, New York 10021, USA
Curr Biol 17:R348-9. 2007
On learning to writeMark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 595, New York, New York 10021, USA
Curr Biol 17:R394-5. 2007
WordsMark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA
Curr Biol 17:R533-5. 2007
RepressorsMark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA
Curr Biol 17:R740-1. 2007
Binding reactions: epigenetic switches, signal transduction and cancerMark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 595, New York, NY 10021, USA
Curr Biol 19:R234-41. 2009..Multiple negative and positive 'add-ons', often with small individual effects, make elementary systems that work, work better. Cancer illustrates various of these fundamental processes gone awry...
A RSC/nucleosome complex determines chromatin architecture and facilitates activator bindingMonique Floer
Molecular Biology Program, Sloan Kettering Institute, 1275 York Avenue, New York, NY 10021, USA
Cell 141:407-18. 2010..Higher eukaryotic RSC lacks the specific DNA-binding determinants found on yeast RSC, and evidently Gal4 works in those organisms despite whatever obstacle broadly positioned nucleosomes present...
HSP90/70 chaperones are required for rapid nucleosome removal upon induction of the GAL genes of yeastMonique Floer
Molecular Biology Program, Sloan Kettering Institute, 1275 York Avenue, New York, NY 10021, USA
Proc Natl Acad Sci U S A 105:2975-80. 2008..Removal of promoter-bound nucleosomes is delayed in a chaperone mutant, and our findings suggest an involvement of HSP90 and HSP70 in this early step in gene induction...
Proteolytic instability and the action of nonclassical transcriptional activatorsXin Wang
Molecular Biology Program, Sloan Kettering Institute, 1275 York Avenue, New York, NY 10021, USA
Curr Biol 20:868-71. 2010..All three are unstable, and for the case analyzed in detail, stabilization decreases activity. Thus, to the extent tested, both classical and nonclassical activators work most efficiently when proteolytically unstable...
Activation of the Gal1 gene of yeast by pairs of 'non-classical' activatorsJason X Cheng
Molecular Biology Program, Sloan Kettering Institute, New York, NY 10021, USA
Curr Biol 14:1675-9. 2004..The results are consistent with the finding that the classical activator Gal4, working at the GAL1 promoter, activates transcription by (at least in part) independently recruiting SAGA and Mediator...
An effect of DNA sequence on nucleosome occupancy and removalXin Wang
Molecular Biology Program, Sloan Kettering Institute, New York, New York, USA
Nat Struct Mol Biol 18:507-9. 2011..As this occupancy is increased (by sequence alteration), nucleosome removal upon induction is decreased, as is mRNA production. These results explain why promoter sequences have evolved to form nucleosomes relatively inefficiently...
Nucleosomes and the accessibility problemXin Wang
Molecular Biology Program, Sloan Kettering Institute, 1275 York Avenue, New York, NY 10065, USA
Trends Genet 27:487-92. 2011..These nucleosomes, evidently, inhibit basal transcription but are poised to be removed quickly upon command...
Two "what if" experimentsMark Ptashne
Sloane Kettering Institute, New York, New York 10021, USA
Cell 116:S71-2, 2 p following S76. 2004
Regulated recruitment and cooperativity in the design of biological regulatory systemsMark Ptashne
Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 595, New York, NY 10021, USA
Philos Trans A Math Phys Eng Sci 361:1223-34. 2003..These are examples of 'regulatory' decisions. A rather simple mechanism - called regulated recruitment - lies at the heart of many of these regulatory decisions...
Independent recruitment in vivo by Gal4 of two complexes required for transcriptionGene O Bryant
Molecular Biology Program, Sloan-Kettering Institute, New York, NY 10021, USA
Mol Cell 11:1301-9. 2003..Our results are consistent with the notion that a single species of activator, Gal4, separately contacts, and thereby directly recruits, SAGA and Mediator...
Transcription: a mechanism for short-term memoryMark Ptashne
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 595, New York, New York 10021, USA
Curr Biol 18:R25-7. 2008..This memory is conveyed by a cytoplasmically transmitted galactokinase working as a signal transducer...
Transcriptional activating regions target a cyclin-dependent kinaseAseem Z Ansari
Program in Molecular Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10021, USA
Proc Natl Acad Sci U S A 99:14706-9. 2002..The interaction evidently positions each activator, as it activates transcription, so that it gets phosphorylated by SRB10, and thus a common mechanism targets disparate substrates to the kinase...
A target essential for the activity of a nonacidic yeast transcriptional activatorZhen Lu
Molecular Biology Program, Sloan Kettering Institute, New York, NY 10021, USA
Proc Natl Acad Sci U S A 99:8591-6. 2002..P201, unlike the typical yeast acidic activating region, does not work in mammalian cells, which is consistent with the notion that the unique target of P201 (Gal11) is absent from mammalian cells...
Signal transduction. Imposing specificity on kinasesMark Ptashne
Department of Molecular Biology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA
Science 299:1025-7. 2003
Telomere looping permits repression "at a distance" in yeastZafar Zaman
Molecular Biology Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA
Curr Biol 12:930-3. 2002..These and other results indicate that DNA-tethered Tup1 represses by interacting with some component of the transcriptional machinery binding to the promoter, an interaction that is facilitated by the preformed loop at the telomere...
Responses of four yeast genes to changes in the transcriptional machinery are determined by their promotersJason X Cheng
Molecular Biology Program, Sloan-Kettering Institute, New York, NY 10021, USA
Curr Biol 12:1828-32. 2002..These and additional results, including those of others, clarify how disparate activators can work at many different promoters...
Regulation of transcription: from lambda to eukaryotesMark Ptashne
Trends Biochem Sci 30:275-9. 2005
Transcriptional activating regions target attached substrates to a cyclin-dependent kinaseAseem Z Ansari
Department of Biochemistry and Genome Center, University of Wisconsin, Madison, WI 53706, USA
Proc Natl Acad Sci U S A 102:2346-9. 2005..In some cases, residues within the activating regions are also phosphorylated. The results define a mechanism by which a kinase is recruited to alternate substrates with diverse physiological consequences...
A unified nomenclature for protein subunits of mediator complexes linking transcriptional regulators to RNA polymerase IIHenri-Marc Bourbon
Mol Cell 14:553-7. 2004
Design of artificial transcriptional activators with rigid poly-L-proline linkersParamjit S Arora
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA
J Am Chem Soc 124:13067-71. 2002..We find that there is an optimal linker length which separates the DNA and the activation region for transcription activation...
RNA sequences that work as transcriptional activating regionsShamol Saha
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA
Nucleic Acids Res 31:1565-70. 2003..The result shows that although all natural activating regions characterized thus far are peptidic, this function can be served by other kinds of moieties as well...
