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SUPT3H-less SAGA coactivator can assemble and function without significantly perturbing RNA polymerase II transcription in mammalian cells
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Supt3 mutant nascent RNA-seq
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ATAC-seq, H3K9ac ChIP-seq and 4sU-seq in WT, SAGA and ATAC mutant mouse embryonic stem cells
Newly synthesized RNA analysis in WT, SAGA and ATAC mutant mouse embryonic stem cells
H3K9ac ChIP-seq in WT, SAGA and ATAC mutant mouse embryonic stem cells
ATAC-seq in WT, SAGA and ATAC mutant mouse embryonic stem cells
The SAGA coactivator regulates the expression of nearly all genes transcribed by RNA polymerase II
SAGA Is a General Cofactor for RNA Polymerase II Transcription
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The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription
The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription [Yeast cells]
The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription [HeLa cells]
Post-transcription initiation function of the ubiquitous SAGA complex in tissue-specific gene activation
Post-transcription initiation function of the ubiquitous SAGA complex in tissue-specific gene activation (gene expression)
Post-transcription initiation function of the ubiquitous SAGA complex in tissue-specific gene activation (ChIP-seq)
Spt3 and Spt8 are involved in the formation of a silencing boundary by interacting with TATA-binding protein
Prp5-Spt8/Spt3 Interaction Mediates a Reciprocal Coupling between Splicing and Transcription
Histone H2Bub1 deubiquitylation is essential for mouse development, but does not regulate global RNA
Histone H2Bub1 deubiquitylation is essential for mouse development, but does not regulate global RNA [ChIP-Seq]
Histone H2Bub1 deubiquitylation is essential for mouse development, but does not regulate global RNA [RNA-Seq]
Acetylation-dependent Multimerization of SAGA Regulates Gene Transcription
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