Étude de la variante d’histone H2A.Z et du cycle de phosphorylation de l’ARN polymérase II chez Saccharomyces cerevisiae
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Summary
The work covered in this thesis addresses two aspects of transcription: the chromatin substrate, with the localization of H 2A variant, H2A.Z, and the transcription complex with the phosphorylation cycle of the RNAPolII CTD, which leads to a better understanding of chromatin function in nuclear phenomena.
- Published
- 2012-10-11
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- https://api.semanticscholar.org/CorpusID:83063656
References
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- The Saccharomyces cerevisiae linker histone Hho1p, with two globular domains, can simultaneously bind to two four-way junction DNA molecules.
- SAS-mediated acetylation of histone H4 Lys 16 is required for H2A.Z incorporation at subtelomeric regions in Saccharomyces cerevisiae.
- Phosphorylation and functions of the RNA polymerase II CTD.
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- DSIF and RNA Polymerase II CTD Phosphorylation Coordinate the Recruitment of Rpd3S to Actively Transcribed Genes
- Ssu72 Is an RNA polymerase II CTD phosphatase.
- MAT1, cdk7 and cyclin H form a kinase complex which is UV light‐sensitive upon association with TFIIH.
- Opening of an RNA polymerase II promoter occurs in two distinct steps and requires the basal transcription factors IIE and IIH.
- Investigating RNA polymerase II carboxyl-terminal domain (CTD) phosphorylation.
- Purification of RNA polymerase IIO from calf thymus.
- Transcription. Seven ups the code.
- Factors involved in specific transcription by mammalian RNA polymerase II. Purification and subunit composition of transcription factor IIF.
- Phosphorylation of RNA polymerase IIA occurs subsequent to interaction with the promoter and before the initiation of transcription.
- Global analysis for functional residues of histone variant Htz1 using the comprehensive point mutant library
- Regions of variant histone His2AvD required for Drosophila development
- The transition of RNA polymerase II from initiation to elongation is associated with phosphorylation of the carboxyl-terminal domain of subunit IIa.
- Comparative genomics of cyclin-dependent kinases suggest co-evolution of the RNAP II C-terminal domain and CTD-directed CDKs
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