samsn1a notes
Provenance and setup
- Record: B3DH22 (TrEMBL, 621 aa), ZFIN ZDB-GENE-030131-8639, Ensembl ENSDARG00000054543 (chr15).
- Paralog: samsn1b (A0A8M2BH30). Pair drawn at random for DANRE_DUPLICATION batch 4
(PANTHER TGD_tree, Ensembl Compara duplication node Osteoglossocephalai).
- Deep research was not available for this gene (Edison returned 402 Payment Required; the OpenAI
key is invalid). Literature was searched by hand through Europe PMC (queries: samsn1a OR samsn1b;
(samsn1 OR HACS1 OR SASH2 OR NASH1) AND zebrafish; title search for HACS1/SAMSN1/NASH1).
- No functional study of zebrafish samsn1a or samsn1b exists. Zebrafish mentions are marker-gene
statements in single-cell RNA-seq papers.
Mammalian SAMSN1 (HACS1, SLy2, NASH1)
Zebrafish / teleost expression
- Retinal bipolar-cell marker in two independent zebrafish scRNA-seq studies:
PMID:37988404
PMID:36047082
- Channel catfish spleen single-nucleus data place samsn1a in a myeloid cluster (catfish, an
otophysan like zebrafish; not zebrafish data):
PMID:39325796
- My analysis (file:DANRE/samsn1a/samsn1a-bioinformatics/RESULTS.md):
- ZFIN curated in situ (Covassin et al. 2006, ZDB-PUB-060927-11): samsn1a in blood, macrophage and
solid lens vesicle at prim-5. samsn1b: epiphysis (pineal) and retinal photoreceptor layer
(Thisse et al. 2004 direct submission).
- E-ERAD-475: samsn1a zygotic, rising from hatching to 28 TPM at day 5; samsn1b has a small
gastrula peak (5 TPM) then silent until larval stages (10-17 TPM).
- Bgee: both copies have RNA-seq calls in granulocyte, spleen, head kidney, retina, gill, intestine,
liver; samsn1a has top scores in granulocyte/spleen/head kidney, samsn1b in retina.
Protein
- samsn1a and samsn1b are only 37.8% identical over the full length, but SH3 domains are 82.3% and
77.4% identical to human SAMSN1 SH3; both keep the 14-3-3 motif region. Both zebrafish proteins
(621/676 aa) and the gar protein (690 aa) are much longer than human SAMSN1 (373 aa).
No relative-rate asymmetry (gar outgroup).
Annotation decisions
- Only two IBA process rows on each copy. Both accepted; the B-cell row is a phylogenetic inference
from the mouse knockout, consistent with the hematopoietic expression of both copies. No NEW rows.