RENT1 RNA-dependent helicase and ATPase required for nonsense-mediated decay (NMD) of mRNAs containing premature stop codons. Is recruited to mRNAs upon translation termination and undergoes a cycle of phosphorylation and dephosphorylation; its phosphorylation appears to be a key step in NMD. Recruited by release factors to stalled ribosomes together with the SMG1C protein kinase complex to form the transient SURF (SMG1-UPF1-eRF1-eRF3) complex. In EJC-dependent NMD, the SURF complex associates with the exon junction complex (EJC) (located 50-55 or more nucleotides downstream from the termination codon) through UPF2 and allows the formation of an UPF1-UPF2-UPF3 surveillance complex which is believed to activate NMD. Phosphorylated UPF1 is recognized by EST1B/SMG5, SMG6 and SMG7 which are thought to provide a link to the mRNA degradation machinery involving exonucleolytic and endonucleolytic pathways, and to serve as adapters to protein phosphatase 2A (PP2A), thereby triggering UPF1 dephosphorylation and allowing the recycling of NMD factors. UPF1 can also activate NMD without UPF2 or UPF3, and in the absence of the NMD-enhancing downstream EJC indicative for alternative NMD pathways. Plays a role in replication-dependent histone mRNA degradation at the end of phase S; the function is independent of UPF2. For the recognition of premature termination codons (PTC) and initiation of NMD a competitive interaction between UPF1 and PABPC1 with the ribosome-bound release factors is proposed. The ATPase activity of UPF1 is required for disassembly of mRNPs undergoing NMD. Essential for embryonic viability. Belongs to the DNA2/NAM7 helicase family. Ubiquitous. 2 alternatively spliced human isoforms have been reported. Note: This description may include information from UniProtKB.
Protein type: C2H2-type zinc finger protein; EC 3.6.1.-; EC 3.6.4.-; Hydrolase; RNA-binding
Chromosomal Location of Human Ortholog: 8 B3.3|8 34.15 cM
Cellular Component:  chromatin; cytoplasm; exon-exon junction complex; nuclear chromosome, telomeric region; nucleoplasm; nucleus; supraspliceosomal complex
Molecular Function:  ATP binding; ATP-dependent RNA helicase activity; chromatin binding; DNA binding; helicase activity; hydrolase activity; metal ion binding; nucleotide binding; protein binding; RNA binding; telomeric DNA binding; zinc ion binding
Biological Process:  3'-UTR-mediated mRNA destabilization; cell cycle phase transition; cellular response to interleukin-1; cellular response to lipopolysaccharide; DNA repair; DNA replication; dosage compensation by inactivation of X chromosome; histone mRNA catabolic process; nuclear-transcribed mRNA catabolic process; nuclear-transcribed mRNA catabolic process, endonucleolytic cleavage-dependent decay; nuclear-transcribed mRNA catabolic process, nonsense-mediated decay; positive regulation of mRNA catabolic process; regulation of telomere maintenance; regulation of translational termination; telomere maintenance via semi-conservative replication
Reference #:  Q9EPU0 (UniProtKB)
Alt. Names/Synonyms: ATP-dependent helicase RENT1; B430202H16Rik; mUpf1; Nonsense mRNA reducing factor 1; NORF1; PNO; PNORF-1; Regulator of nonsense transcripts 1; Regulator of nonsense transcripts 1 (Nonsense mRNA reducing factor 1) (NORF1) (Up-frameshift suppressor 1 homolog); Ren; Rent1; Up-frameshift suppressor 1 homolog; Upf1; UPF1 regulator of nonsense transcripts homolog (yeast); Upflp
Gene Symbols: Upf1
Molecular weight: 123,967 Da
Basal Isoelectric point: 6.18  Predict pI for various phosphorylation states
Protein-Specific Antibodies, siRNAs or Recombinant Proteins from Cell Signaling Technology® Total Proteins
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RENT1

Protein Structure Not Found.


Cross-references to other databases:  STRING  |  Reactome  |  BioGPS  |  Pfam  |  ENZYME  |  Phospho.ELM  |  NetworKIN  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene  |  Ensembl Protein