cep-1 notes
2026-09-30
- Completed the worm cep-1 review as the final C. elegans CED-pathway comparator
in the APOPTOSIS slice. CEP-1 was curated as the nuclear p53-family
sequence-specific transcription activator that induces egl-1 and ced-13
BH3-only transcription after genotoxic stress, engaging the
CED-9/CED-4/CED-3 intrinsic apoptosis module. The core DNA-damage branch is
supported by the original cep-1 germline-apoptosis paper PMID:11696333,
the HUS-1/egl-1 checkpoint paper PMID:12445383, the ced-13 induction paper
PMID:15605074, UV-C and genome-wide transcriptional profiling studies
[PMID:17347667; PMID:18627611], and PRMT-5/CBP-1 modulation of
CEP-1-dependent egl-1 induction PMID:19521535.
- Tightened generic transcription rows.
GO:0003677 DNA binding,
GO:0003700 DNA-binding transcription factor activity, and broad
GO:0006355 regulation of DNA-templated transcription rows were moved toward
GO:0001228 DNA-binding transcription activator activity, RNA polymerase
II-specific or GO:0045944 positive regulation of transcription by RNA
polymerase II, using the CEP-1 p53 response-element evidence from the DNA
binding-domain and fasn-1 target-gene studies [PMID:15242600;
PMID:16582625].
- Kept the PRMT-5/CBP-1 transcription repressor complex as a real but non-core
regulatory assembly, kept ER-stress/IRE-1-triggered p53-mediated germline
apoptosis as a non-DNA-damage branch, and retained hypoxia, starvation,
lifespan, and meiotic chromosome-segregation rows as non-core stress or
genome-quality phenotypes rather than direct apoptotic outputs.
- Marked the SMG-1 paraquat row to
GO:0006979 response to oxidative stress
as over-annotated for CEP-1: smg-1 inactivation produces cep-1-dependent
oxidative-stress resistance, but the experiment is an endpoint epistasis
assay and does not show that CEP-1 itself directly executes an oxidative
stress response PMID:18836529.
- Left four rows unresolved pending full-text or structural evidence: the old
RAD-51 IGI apoptosis row from an abstract-only rad-51 paper
PMID:12684824, the two zinc-binding rows whose direct seeded paper concerns
the C-terminal oligomerization/SAM domain PMID:17581633, and the old
nucleolus localization row from the abstract-only founding CEP-1 paper
PMID:11557844.