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Identification of Regions in the Spt5 Subunit of DRB Sensitivity-inducing Factor (DSIF) That Are Involved in Promoter-proximal Pausing.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2017 Mar 31; Vol. 292 (13), pp. 5555-5570. Date of Electronic Publication: 2017 Feb 17. - Publication Year :
- 2017
-
Abstract
- DRB sensitivity-inducing factor (DSIF or Spt4/5) is a conserved transcription elongation factor that both inhibits and stimulates transcription elongation in metazoans. In Drosophila and vertebrates, DSIF together with negative elongation factor (NELF) associates with RNA polymerase II during early elongation and causes RNA polymerase II to pause in the promoter-proximal region of genes. The mechanism of how DSIF establishes pausing is not known. We constructed Spt5 mutant forms of DSIF and tested their capacity to restore promoter-proximal pausing to DSIF-depleted Drosophila nuclear extracts. The C-terminal repeat region of Spt5, which has been implicated in both inhibition and stimulation of elongation, is dispensable for promoter-proximal pausing. A region encompassing KOW4 and KOW5 of Spt5 is essential for pausing, and mutations in KOW5 specifically shift the location of the pause. RNA cross-linking analysis reveals that KOW5 directly contacts the nascent transcript, and deletion of KOW5 disrupts this interaction. Our results suggest that KOW5 is involved in promoter-proximal pausing through contact with the nascent RNA.<br /> (© 2017 by The American Society for Biochemistry and Molecular Biology, Inc.)
- Subjects :
- Animals
Chromosomal Proteins, Non-Histone metabolism
Drosophila genetics
Protein Binding
Protein Subunits
Transcription Factors metabolism
Transcriptional Elongation Factors metabolism
Drosophila Proteins metabolism
Nuclear Proteins metabolism
Promoter Regions, Genetic physiology
Protein Interaction Domains and Motifs
RNA Polymerase II metabolism
Transcription, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 1083-351X
- Volume :
- 292
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28213523
- Full Text :
- https://doi.org/10.1074/jbc.M116.760751