CREBBP
Overview
CREBBP mutations are highly prevalent in both DLBCL and FL.pasqualucciInactivatingMutationsAcetyltransferase2011a? These mutations often affect the histone acetyltransferase (HAT) domain, crucial for regulating gene expression through chromatin modification, or generate a truncated protein.1 This gene has some recurrent sites of mutations (hotspots), mostly in the HAT domain. The pattern of mutations in DLBCL is distinct from FL with the latter having more HAT domain mutations relative to truncating mutations.1
History
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timeline
title Publication timing
2011-03-10 : Pasqualucci : DLBCL
2012-12-01 : Love : BL
2013-12-13 : Parry : MZL
2021-07-15 : Duns : PMBL
Relevance tier by entity
| Entity | Tier | Description |
|---|---|---|
| 2 | relevance in MZL not firmly established2 | |
| 1 | high-confidence PMBL/cHL/GZL genedunsCharacterizationDLBCLPMBL2021b? | |
| 1 | high-confidence DLBCL genepasqualucciInactivatingMutationsAcetyltransferase2011a? | |
| 1 | high-confidence FL genepasqualucciInactivatingMutationsAcetyltransferase2011a? | |
| 2 | association with BL is tenuous3 |
Mutation incidence in large patient cohorts (GAMBL reanalysis)
| Entity | source | frequency (%) |
|---|---|---|
| DLBCL | GAMBL genomes | 25.81 |
| DLBCL | Schmitz cohort | 17.87 |
| DLBCL | Reddy cohort | 12.11 |
| DLBCL | Chapuy cohort | 16.67 |
| FL | GAMBL genomes | 65.13 |
| BL | GAMBL genomes+capture | 6.00 |
| BL | Thomas cohort | 3.00 |
| BL | Panea cohort | 12.90 |
Mutation pattern and selective pressure estimates
| Entity | aSHM | Significant selection | dN/dS (missense) | dN/dS (nonsense) |
|---|---|---|---|---|
| BL | No | No | 1.357 | 3.999 |
| DLBCL | No | Yes | 13.231 | 65.302 |
| FL | No | Yes | 43.869 | 112.938 |
CREBBP Hotspots
| Chromosome | Coordinate (hg19) | ref>alt | HGVSp |
|---|---|---|---|
| chr16 | 3788618 | G>A | R1446C |
| chr16 | 3788617 | C>T | R1446H |
| chr16 | 3788617 | C>A | R1446L |
| chr16 | 3788606 | A>T | Y1450N |
| chr16 | 3788606 | A>C | Y1450D |
| chr16 | 3788605 | T>G | Y1450S |
| chr16 | 3788605 | T>C | Y1450C |
| chr16 | 3788596 | A>G | I1453T |
| chr16 | 3788594 | G>T | L1454I |
| chr16 | 3788593 | A>C | L1454R |
| chr16 | 3786715 | A>T | L1499Q |
| chr16 | 3786715 | A>G | L1499P |
| chr16 | 3786715 | A>C | L1499R |
| chr16 | 3786710 | C>A | E1501* |
| chr16 | 3786707 | A>T | W1502R |
| chr16 | 3786707 | A>G | W1502R |
| chr16 | 3786705 | C>T | W1502* |
| chr16 | 3786705 | C>G | W1502C |
| chr16 | 3786705 | C>A | W1502C |
| chr16 | 3786704 | A>T | Y1503N |
| chr16 | 3786704 | A>G | Y1503H |
| chr16 | 3786704 | A>C | Y1503D |
| chr16 | 3786703 | T>G | Y1503S |
| chr16 | 3786703 | T>A | Y1503F |
| chr16 | 3786691 | A>G | L1507P |
View coding variants in ProteinPaint hg19 or hg38
View all variants in GenomePaint hg19 or hg38
CREBBP Expression
References
1.
Dreval K, Hilton LK, Cruz M, Shaalan H,
Ben-Neriah S, Boyle M, Collinge B, Coyle KM, Duns G, Farinha P, Grande
BM, Meissner B, Pararajalingam P, Rushton CK, Slack GW, Wong J, Mungall
AJ, Marra MA, Connors JM, Steidl C, Scott DW, Morin RD. Genetic
subdivisions of follicular lymphoma defined by distinct coding and
noncoding mutation patterns. Blood. 2023 Aug 10;142(6):561–573. PMCID:
PMC10644066
2.
Parry M, Rose-Zerilli MJJ, Gibson J, Ennis S,
Walewska R, Forster J, Parker H, Davis Z, Gardiner A, Collins A, Oscier
DG, Strefford JC. Whole exome sequencing identifies novel recurrently
mutated genes in patients with splenic marginal zone lymphoma. PLoS One.
2013;8(12):e83244. PMCID: PMC3862727
3.
Love
C, Sun Z, Jima D, Li G, Zhang J, Miles R, Richards KL, Dunphy CH, Choi
WWL, Srivastava G, Lugar PL, Rizzieri DA, Lagoo AS, Bernal-Mizrachi L,
Mann KP, Flowers CR, Naresh KN, Evens AM, Chadburn A, Gordon LI, Czader
MB, Gill JI, Hsi ED, Greenough A, Moffitt AB, McKinney M, Banerjee A,
Grubor V, Levy S, Dunson DB, Dave SS. The genetic landscape of mutations
in Burkitt lymphoma. Nat Genet. 2012 Dec;44(12):1321–1325.
PMCID: PMC3674561


