Basic Information
Gene ID
Ciclev10009459m.g.v1.0
Position
scaffold_1:11258635-11261886 (-)
3251bp
Gene Type
gene
Gene Description (Protein Product)
Cleavage and polyadenylation specificity factor subunit
Organism
Also AS AT4G29820CICLE_v10009459mg

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Ciclev10014454m.g.v1.0 Cleavage and polyadenylation specificity factor
Ciclev10011737m.g.v1.0 Required for endonucleolytic cleavage during polyadenylation-dependent pre-mRNA 3'-end formation
Ciclev10023968m.g.v1.0 Cleavage stimulation factor subunit
Regulatory gene
Ciclev10001376m.g.v1.0 tesmin TSO1-like CXC
Ciclev10001952m.g.v1.0 Zinc-finger homeodomain protein
Ciclev10002179m.g.v1.0 dof zinc finger protein

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail


Pathway
KEGG Term Name Description
map03015 mRNA surveillance pathway The mRNA surveillance pathway is a quality control mechanism that detects and degrades abnormal mRNAs. These pathways include nonsense-mediated mRNA decay (NMD), nonstop mRNA decay (NSD), and no-go decay (NGD). NMD is a mechanism that eliminates mRNAs containing premature translation-termination codons (PTCs). In vertebrates, PTCs trigger efficient NMD when located upstream of an exon junction complex (EJC). Upf3, together with Upf1 and Upf2, may signal the presence of the PTC to the 5'end of the transcript, resulting in decapping and rapid exonucleolytic digestion of the mRNA. In the NSD pathway, which targets mRNAs lacking termination codons, the ribosome is believed to translate through the 3' untranslated region and stall at the end of the poly(A) tail. NSD involves an eRF3-like protein, Ski7p, which is hypothesized to bind the empty A site of the ribosome and recruit the exosome to degrade the mRNA from the 3' end. NGD targets mRNAs with stalls in translation elongation for endonucleolytic cleavage in a process involving the Dom34 and Hbs1 proteins.