Spt6 is an essential transcription elongation factor and histone chaperone that binds the C-terminal repeat domain (CTD) of RNA polymerase II. We show here that Spt6 contains a tandem SH2 domain with a novel structure and CTD-binding mode. The tandem SH2 domain binds to a serine 2-phosphorylated CTD peptide in vitro, whereas its N-terminal SH2 subdomain, which we previously characterized, does not. CTD binding requires a positively charged crevice in the C-terminal SH2 subdomain, which lacks the canonical phospho-binding pocket of SH2 domains and had previously escaped detection. The tandem SH2 domain is apparently required for transcription elongation in vivo as its deletion in cells is lethal in the presence of 6-azauracil
In different phases of the transcription cycle, RNA polymerase (Pol) II recruits various factors via...
Transcription elongation by RNA polymerase II is regulated by an array of protein complexes. Among v...
La plus grosse sous-unité (Rpb1) de l'ARN polymérase II est caractérisée par une structure unique et...
During transcription elongation through chromatin, the Ser2-phosphorylated C-terminal repeat domain ...
The C-terminal domain (CTD) of RNA polymerase II is sequentially modified for recruitment of numerou...
During mRNA elongation, the SRI domain of the histone H3 methyltransferase Set2 binds to the phospho...
During mRNA elongation, the SRI domain of the histone H3 methyltransferase Set2 binds to the phospho...
Spt6 is a histone chaperone that associates with RNA polymerase II and deposits nucleosomes in the w...
Transcription from a most basic perspective is the process of generating strands of RNA from DNA tem...
Phosphorylation of the C-terminal domain of RNA polymerase II controls the co-transcriptional assemb...
Transcription elongation factor Spt6 associates with RNA polymerase II (Pol II) and acts as a histon...
The C-terminal domain (CTD) of RNA polymerase II (Pol II) integrates nuclear events by binding prote...
In different phases of the transcription cycle, RNA polymerase (Pol) II recruits various factors via...
SummaryTranscription controls splicing and other gene regulatory processes, yet mechanisms remain ob...
Phosphorylation patterns of the C-terminal domain (CTD) of largest subunit of RNA polymerase II (cal...
In different phases of the transcription cycle, RNA polymerase (Pol) II recruits various factors via...
Transcription elongation by RNA polymerase II is regulated by an array of protein complexes. Among v...
La plus grosse sous-unité (Rpb1) de l'ARN polymérase II est caractérisée par une structure unique et...
During transcription elongation through chromatin, the Ser2-phosphorylated C-terminal repeat domain ...
The C-terminal domain (CTD) of RNA polymerase II is sequentially modified for recruitment of numerou...
During mRNA elongation, the SRI domain of the histone H3 methyltransferase Set2 binds to the phospho...
During mRNA elongation, the SRI domain of the histone H3 methyltransferase Set2 binds to the phospho...
Spt6 is a histone chaperone that associates with RNA polymerase II and deposits nucleosomes in the w...
Transcription from a most basic perspective is the process of generating strands of RNA from DNA tem...
Phosphorylation of the C-terminal domain of RNA polymerase II controls the co-transcriptional assemb...
Transcription elongation factor Spt6 associates with RNA polymerase II (Pol II) and acts as a histon...
The C-terminal domain (CTD) of RNA polymerase II (Pol II) integrates nuclear events by binding prote...
In different phases of the transcription cycle, RNA polymerase (Pol) II recruits various factors via...
SummaryTranscription controls splicing and other gene regulatory processes, yet mechanisms remain ob...
Phosphorylation patterns of the C-terminal domain (CTD) of largest subunit of RNA polymerase II (cal...
In different phases of the transcription cycle, RNA polymerase (Pol) II recruits various factors via...
Transcription elongation by RNA polymerase II is regulated by an array of protein complexes. Among v...
La plus grosse sous-unité (Rpb1) de l'ARN polymérase II est caractérisée par une structure unique et...