exoc3l2a notes
Setup and provenance
- Fetched with
just fetch-gene on A0A8N7TEH3 (TrEMBL, RefSeq XP_683981.7, "Exocyst complex
component 3-like protein 2", 932 aa); 5 GOA rows (3 IBA, 2 IEA), none with a PMID. The GOA
gene-name column reads "Tumor necrosis factor alpha-induced protein 2-like", which reflects
PANTHER's subfamily naming (PTHR21292:SF18, "TUMOR NECROSIS FACTOR ALPHA-INDUCED PROTEIN 2"), not
the orthology (see below). ZFIN ZDB-GENE-060526-343, Ensembl ENSDARG00000008414, chromosome 5.
- Deep research unavailable: Edison returned 402 Payment Required and the OpenAI key is
invalid, so no -deep-research-*.md file exists. Literature searched by hand via Europe PMC
(queries: exoc3l2a OR exoc3l2b, EXOC3L2, TITLE:"exocyst complex component 3-like 2",
EXOC3L2 AND endothelial AND migration, exoc3l2 AND zebrafish, EXOC3L4).
- DANRE_DUPLICATION random sample, draw 4 (seed 20260928); paralog exoc3l2b.
Which human gene is this an ortholog of?
- ZFIN/Ensembl name the gene after EXOC3L2, and Ensembl Compara calls human EXOC3L2 an
ortholog (one-to-many, Euteleostomi) and places the exoc3l2a/exoc3l2b duplication at
Osteoglossocephalai, with one gar ortholog (ENSLOCG00000014731) for both copies
(file:DANRE/exoc3l2a/exoc3l2a-bioinformatics/RESULTS.md).
- PANTHER's TGD table lists EXOC3L4 as the human ortholog, and PANTHER's HMM assigns the
zebrafish proteins to TNFAIP2-named subfamilies (SF18/SF17) while human EXOC3L2 is in SF7.
- My alignment: exoc3l2a is 35.3% identical to human EXOC3L2 but only 19.7-21.8% to EXOC3,
EXOC3L1, EXOC3L4 and TNFAIP2; zebrafish also has its own exoc3l4, tnfaip2a/b and exoc3l1
genes, which are all ~17-22% identical to exoc3l2a. The gar and medaka orthologs show the same
pattern (35-39% to EXOC3L2). Conclusion: exoc3l2a is an EXOC3L2 co-ortholog; the PANTHER
EXOC3L4 label is not supported by sequence. (RESULTS.md)
Zebrafish literature
- Endothelial expression at 24 hpf (AngioTag TRAP-seq + WISH):
PMID:40613926.
Figure legend gives the stage: PMID:40613926 (sic).
- Part of the caudal hematopoietic tissue (CHT) vascular-niche endothelial signature:
PMID:37119815
- No mutant, morphant or protein-level study. ZFIN has no curated wild-type expression rows.
Mammalian EXOC3L2 (the single-copy ortholog)
- Human endothelial cells: associates with exocyst, needed for VEGFR2 phosphorylation and
directional migration PMID:21566143
PMID:21566143
Vascular expression in mouse brain: PMID:21566143
- Mouse knockout: embryonic lethal with hemorrhage; endothelial/hematopoietic (Tie2-Cre)
deletion reproduces it PMID:36362885
PMID:36362885
Dispensable for postnatal retinal angiogenesis PMID:36362885
Mouse expression also in probable cranial neural crest PMID:36362885
- Human disease: PMID:30327448
- Structure: EXOC3L2 is a paralog of M-Sec/TNFAIP2 and may bind RalA; whether it is an
exocyst subunit or acts independently is open PMID:30086153
Note: PMID:30086153 uses "Exoc3l2a" for a mouse splice variant; unrelated to the zebrafish gene name.
- Human EXOC3L2 in GOA (QuickGO, 2026-09-28) has only IEA exocyst/exocytosis rows and IPI
protein-binding rows; it carries no IBA from PTN000480155, whereas human EXOC3, EXOC3L1,
EXOC3L4 and TNFAIP2 do. So in PANTHER the zebrafish copies sit with the paralogs that inherit
the node, not with human EXOC3L2 (consistent with the PANTHER EXOC3L4 call).
See RESULTS.md. Key points: 50.9% identity between the copies; exoc3l2a carries about twice as
many lineage-specific changes as exoc3l2b relative to gar (138 vs 71; chi2 21.5); both keep a
full-length Sec6 domain; similar whole-embryo time courses; broadly overlapping adult Bgee calls.
Annotation decisions
- exocyst (IBA, IEA): accepted; mammalian EXOC3L2 co-precipitates with EXOC4 and colocalises
with EXOC4/EXOC7, and the Sec6 domain is intact. Membership of the canonical octamer is not
shown, so association rather than stoichiometric subunit.
- exocytosis (IBA, IEA): kept as non-core; no secretion assay for EXOC3L2 in any species.
- SNARE binding (IBA): marked over-annotated; the only experimental donor is yeast Sec6.