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GeneE
8 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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BRME1
break repair meiotic recombinase recruitment factor 1
Chromosome 19 · 19p13.12
NCBI Gene: 79173Ensembl: ENSG00000132016.12HGNC: HGNC:28153UniProt: K7EMZ7
25PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingfemale meiosis Ispermatogenesisdouble-strand break repair involved in meiotic recombinationHodgkins lymphomagenetic disorderautosomal recessive non-syndromic intellectual disabilityazoospermia
✦AI Summary

BRME1 (break repair meiotic recombinase recruitment factor 1) is a meiosis-specific protein essential for homologous recombination during germ cell development. Mechanistically, BRME1 functions as a stabilizer of the MEILB2 protein, preventing its self-association and enabling formation of the BRCA2-MEILB2-BRME1 ternary complex 1. This complex recruits and concentrates the recombinases RAD51 and DMC1 at meiotic double-strand break (DSB) sites 2. Structurally, BRME1 and MEILB2 form a V-shaped DNA clamp upon BRCA2 binding, with DNA-binding β-caps separated by 25 nm that bridge resected DNA ends to facilitate recombination 3. Additionally, BRME1 controls HSF2BP-BRCA2 oligomerization, ensuring timely assembly of recombination complexes 4. Loss of BRME1 destabilizes the BRCA2-MEILB2 complex, causing defective DSB repair, impaired homolog synapsis, and reduced crossover formation 1. Clinically, BRME1 mutations and reduced expression associate with primary ovarian insufficiency and male infertility 25. Beyond meiosis, somatic MEILB2-BRME1 expression in cancer cells impairs mitotic homologous recombination 1, and BRME1 expression correlates with cisplatin responsiveness in head and neck cancers 6.

Sources cited
1
BRME1 interacts with and stabilizes HSF2BP, forms complex with BRCA2 and RAD51, and mutations cause primary ovarian insufficiency with reduced crossover formation
PMID: 32845237
2
BRME1 stabilizes MEILB2 and is part of BRCA2-MEILB2-BRME1 ternary complex; Brme1 knockout causes DSB repair defects and crossover formation defects; ectopic somatic expression impairs mitotic HR
PMID: 32345962
3
BRCA2 associates with meiosis-specific cofactors to facilitate homologous recombination in germ cells
PMID: 34625364
4
BRME1/C19orf57 is differentially expressed between HPV+ and HPV- head and neck cancers and correlates with cisplatin responsiveness
PMID: 36857322
5
BRME1 controls HSF2BP-BRCA2 oligomerization and ring dissociation to promote homologous recombination
PMID: 37889963
6
MEILB2-BRME1 forms V-shaped DNA clamp with β-caps separated by 25 nm upon BRCA2 binding to bridge DNA molecules
PMID: 39095423
7
PCBP2 regulates Brme1 mRNA stability and splicing; Brme1 is critical for meiotic progression and spermatogenesis
PMID: 41655928
Disease Associationsⓘ20
Hodgkins lymphomaOpen Targets
0.19Weak
genetic disorderOpen Targets
0.16Weak
autosomal recessive non-syndromic intellectual disabilityOpen Targets
0.15Weak
azoospermiaOpen Targets
0.10Suggestive
partial chromosome Y deletionOpen Targets
0.09Suggestive
spermatogenic failure 57Open Targets
0.09Suggestive
spermatogenic failure 50Open Targets
0.09Suggestive
spermatogenic failure 25Open Targets
0.08Suggestive
spermatogenic failure, X-linked, 2Open Targets
0.08Suggestive
spermatogenic failure 71Open Targets
0.08Suggestive
isochromosomy YpOpen Targets
0.08Suggestive
spermatogenic failure 59Open Targets
0.08Suggestive
spermatogenic failure 60Open Targets
0.08Suggestive
spermatogenic failure 73Open Targets
0.08Suggestive
spermatogenic failure 74Open Targets
0.08Suggestive
spermatogenic failure 61Open Targets
0.08Suggestive
spermatogenic failure 62Open Targets
0.08Suggestive
spermatogenic failure 88Open Targets
0.08Suggestive
spermatogenic failure 48Open Targets
0.08Suggestive
spermatogenic failure 63Open Targets
0.08Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
HSF2BPProtein interaction63%SPMIP7Shared pathway33%CBY3Shared pathway33%ARRDC5Shared pathway33%C3orf62Shared pathway33%TXNDC8Shared pathway33%
Tissue Expression6 tissues
Bone Marrow
100%
Brain
49%
Ovary
26%
Liver
14%
Lung
8%
Heart
8%
Gene Interaction Network
Click a node to explore
BRME1HSF2BPSPMIP7CBY3ARRDC5C3orf62TXNDC8
PROTEIN STRUCTURE
Preparing viewer…
PDB8A51 · 1.90 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.81LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.61 [0.46–0.81]
RankingsWhere BRME1 stands among ~20K protein-coding genes
  • #12,943of 20,598
    Most Researched25
  • #6,865of 17,882
    Most Constrained (LOEUF)0.81
Genes detectedBRME1
Sources retrieved8 papers
Response time—
📄 Sources
8▼
1
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1.
PMID: 32845237
Elife · 2020
1.00
2
The BRCA2-MEILB2-BRME1 complex governs meiotic recombination and impairs the mitotic BRCA2-RAD51 function in cancer cells.
PMID: 32345962
Nat Commun · 2020
0.88
3
BRCA2 in mammalian meiosis.
PMID: 34625364
Trends Cell Biol · 2022
0.75
4
Therapeutic implications of transcriptomics in head and neck cancer patient-derived xenografts.
PMID: 36857322
PLoS One · 2023
0.63
5
BRCA2-HSF2BP oligomeric ring disassembly by BRME1 promotes homologous recombination.
PMID: 37889963
Sci Adv · 2023
0.50