Protein / target
B-cell lymphoma 6 protein
Protein at a glance
Biological role
Sequence-specific double-stranded DNA binding
Strongest disease association
Lymphoid neoplasm
Research activity
Emerging research
Derived from structured UniProt, Open Targets and literature data on this page.
Protein profile
Canonical identity and biological annotation from UniProt.
Function overview
Transcriptional repressor mainly required for germinal center (GC) formation and antibody affinity maturation which has different mechanisms of action specific to the lineage and biological functions.
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Transcriptional repressor mainly required for germinal center (GC) formation and antibody affinity maturation which has different mechanisms of action specific to the lineage and biological functions. Forms complexes with different corepressors and histone deacetylases to repress the transcriptional expression of different subsets of target genes. Represses its target genes by binding directly to the DNA sequence 5'-TTCCTAGAA-3' (BCL6-binding site) or indirectly by repressing the transcriptional activity of transcription factors. In GC B-cells, represses genes that function in differentiation, inflammation, apoptosis and cell cycle control, also autoregulates its transcriptional expression and up-regulates, indirectly, the expression of some genes important for GC reactions, such as AICDA, through the repression of microRNAs expression, like miR155. An important function is to allow GC B-cells to proliferate very rapidly in response to T-cell dependent antigens and tolerate the physiological DNA breaks required for immunoglobulin class switch recombination and somatic hypermutation without inducing a p53/TP53-dependent apoptotic response. In follicular helper CD4(+) T-cells (T(FH) cells), promotes the expression of T(FH)-related genes but inhibits the differentiation of T(H)1, T(H)2 and T(H)17 cells. Also required for the establishment and maintenance of immunological memory for both T- and B-cells. Suppresses macrophage proliferation through competition with STAT5 for STAT-binding motifs binding on certain target genes, such as CCL2 and CCND2. In response to genotoxic stress, controls cell cycle arrest in GC B-cells in both p53/TP53-dependedent and -independent manners. Besides, also controls neurogenesis through the alteration of the composition of NOTCH-dependent transcriptional complexes at selective NOTCH targets, such as HES5, including the recruitment of the deacetylase SIRT1 and resulting in an epigenetic silencing leading to neuronal differentiation
Subcellular location
Domains and Gene Ontology detail (34)Hide
Domains & features
Gene Ontology
- Cnucleoplasm
- Cnucleus
- Cparaspeckles
- Fchromatin binding
- Fchromatin DNA binding
- FDNA-binding transcription factor activity
- FDNA-binding transcription factor binding
- FDNA-binding transcription repressor activity, RNA polymerase II-specific
- Fidentical protein binding
- Fintronic transcription regulatory region sequence-specific DNA binding
- FRNA polymerase II cis-regulatory region sequence-specific DNA binding
- Fsequence-specific DNA binding
Biological roles
What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.
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Cell-cycle regulation
- ·Transcriptional repressor mainly required for germinal center (GC) formation and antibod…
- ·negative regulation of mitotic cell cycle DNA replication
Cell proliferation & survival
- ·regulation of cell population proliferation
Immune signalling
- ·Transcriptional repressor mainly required for germinal center (GC) formation and antibod…
- ·inflammatory response
- ·negative regulation of B cell apoptotic process
- ·positive regulation of regulatory T cell differentiation
Transcriptional regulation
- ·Transcriptional repressor mainly required for germinal center (GC) formation and antibod…
- ·DNA-binding transcription factor activity
- ·DNA-binding transcription factor binding
- ·DNA-binding transcription repressor activity, RNA polymerase II-specific
Apoptosis & cell death
- ·negative regulation of B cell apoptotic process
- ·positive regulation of apoptotic process
Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.
Translational evidence
Why this target matters therapeutically, strongest evidence first. Disease associations are gene-level (via the gene that encodes this protein) and open into the full confidence synthesis; the development universe, tractability and safety annotations are target-level, from Open Targets.
Strongest disease associations · via encoding gene BCL6
Gene-level evidence surfaced through the gene BCL6that encodes this protein — not a direct protein–disease relationship. Ranked by Forefront's causal-directness weighting, so genetically- and clinically-evidenced diseases lead over ones that merely share the literature.
View evidence synthesis (5)Hide
This ranking differs from Open Targets' own: re-weighting moves genetically-evidenced diseases above more heavily co-mentioned ones. The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the per-type scores above show the calculation.
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Tractability
Small molecules — Emerging
Protein degraders — Emerging
View underlying tractability evidence (7)Hide
Raw Open Targets tractability assessment buckets, by modality.
Research activity
Papers linked directly to this protein. This is the protein's own literature — descriptor-derived papers are kept separate below.
Most cited
Recent
Europe PMC papers linked directly to this protein.