SPO11
Meiotic recombination protein SPO11
Also known as: CT35, SPATA43, SPO11_HUMAN, TOPOVIA, TOPVIA
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y5K1
- Gene
- SPO11
- Ensembl
- ENSG00000054796
- Chromosome
- 20
- Canonical length
- 396 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Meiotic recombination and chromosome segregation require the formation of double-strand breaks (DSBs) in paired chromosome homologs. During meiosis in yeast, a meiotic recombination protein is covalently-linked to the 5' end of DSBs and is essential for the formation of DSBs. The protein encoded by this gene is similar in sequence and conserved features to the yeast meiotic recombination protein. The encoded protein belongs to the TOP6A protein family. Several transcript variants encoding different isoforms have been found for this gene, but the full-length nature of only two of them have been described. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
396 residues, UniProt reviewed canonical sequence.
>Q9Y5K1|SPO11
1 MAFAPMGPEA SFFDVLDRHR ESLLAALRRG GREPPTGGSR LASSSEVLAS IENIIQDIIT
61 SLARNEAPAF TIDNRSSWEN IKFEDSVGLQ MVSHCTTRKI KSDSPKSAQK FSLILKILSM
121 IYKLVQSNTY ATKRDIYYTD SQLFGNQTVV DNIINDISCM LKVSRRSLHI LSTSKGLIAG
181 NLRYIEEDGT KVNCTCGATA VAVPSNIQGI RNLVTDAKFV LIVEKDATFQ RLLDDNFCNK
241 LSPCIMITGK GVPDLNTRLL VKKLWDTFHV PVFTLVDADP HGIEIMCIYK YGSMSMSFEA
301 HHLTVPAIRW LGLLPSDLKR LNVPKDSLIP LTKRDQMKLD SILRRPYVTC QPFWRKEMEI
361 MADSKMKAEI QALTFLSSDY LSRVYLPNKL KFGGWILocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPO11 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 7.9 nTPM
Expression across tissuesHPA
Tissue
- testis: 7.9 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
- appendix: 0 nTPM
- basal ganglia: 0 nTPM
Single-cell type
- early primary spermatocytes: 109 nCPM
- undifferentiated spermatogonia: 11 nCPM
- late primary spermatocytes: 4.5 nCPM
- late spermatids: 2 nCPM
- differentiating spermatogonia: 1.2 nCPM
- lymphatic endothelial cells: 0.3 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SPO11.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 43 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.11
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.97
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- double-strand break repair involved in meiotic recombination
- female gamete generation
- male meiosis I
- meiotic DNA double-strand break formation
- meiotic telomere clustering
- oogenesis
- ovarian follicle development
- protein localization to chromosome
- reciprocal meiotic recombination
- spermatid development
- spermatogenesis
- synaptonemal complex assembly
- meiotic DNA double-strand break processing
Molecular functions
- ATP binding
- DNA binding
- DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity
- metal ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Winged helix-like DNA-binding domain superfamily
- Spo11/DNA topoisomerase VI subunit A
- Meiosis-specific protein Spo11
- Meiotic recombination, Spo11
- Spo11/DNA topoisomerase VI, subunit A, N-terminal
- Topoisomerase 6 subunit A/Spo11, TOPRIM domain
- Spo11/DNA topoisomerase VI subunit A superfamily
- SPO11 homologue
- Type IIB DNA topoisomerase
- Topoisomerase 6 subunit A/Spo11, Toprim domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPO11 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SPO11 as an antibody target. Whether an autoantibody or antibody against SPO11 could matter depends on whether native SPO11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPO11 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SPO11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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