SEN1 is a superfamily I helicase with key functions in:
Transcription termination: Resolving RNA polymerase II (RNAPII) and III (RNAPIII) transcription complexes
R-loop prevention: Resolving RNA:DNA hybrids to maintain genome stability
Replication fork progression: Interacting with replisome components (e.g., Ctf4, Mrc1) during DNA replication
SEN1 homologs are linked to human diseases:
Senataxin (SETX): Mutations cause ALS4 and ataxia with oculomotor apraxia type 2 .
Mechanism: Defective resolution of R-loops and transcription-replication conflicts .
SEN1 levels fluctuate during the cell cycle:
Degradation in G1: Mediated by ubiquitin-proteasome system .
Stabilization in S/G2: Critical for replication fork progression .
While no SEN1-specific antibody is described in the sources, methodologies include:
Chromatin immunoprecipitation (ChIP-seq): Maps SEN1 binding to RNAPIII-transcribed genes (tRNA, 5S rRNA) .
Temperature-sensitive mutants: sen1-1 (G1747D) used to study transcription termination defects .
CRAC (UV crosslinking and analysis of cDNA): Identifies SEN1-RNAPII interaction sites .
KEGG: sce:YLR430W
STRING: 4932.YLR430W