KMT2D
Histone-lysine N-methyltransferase 2D (KMT2D), also known as MLL4 and sometimes MLL2 in humans and Mll4 in mice, is a major mammalian histone H3 lysine 4 (H3K4) mono-methyltransferase.[5] It is part of a family of six Set1-like H3K4 methyltransferases that also contains KMT2A (or MLL1), KMT2B (or MLL2), KMT2C (or MLL3), KMT2F (or SET1A), and KMT2G (or SET1B).
KMT2D is a large
Mutations in KMT2D cause human genetic conditions including Kabuki syndrome,[16] another distinct congenital malformations disorder[17] and various forms of cancer.[18]
Structure
Gene
In mice, KMT2D is coded by the Kmt2d gene located on chromosome 15F1. Its transcript is 19,823 base pairs long and contains 55 exons and 54 introns.[19]
In humans, KMT2D is coded by the KMT2D gene located on chromosome 12q13.12. It's transcript is 19,419 base pairs long and contains 54 exons and 53 introns.[20]
Protein
KMT2D is homologous to Trithorax-related (Trr), which is a
Protein complex
Several components of the KMT2D complex were first purified in 2003,[25] and then the entire complex was identified in 2007.[26][27][28][29] Along with KMT2D, the complex also contains ASH2L, RbBP5, WDR5, DPY30, NCOA6, UTX (also known as KDM6A), PA1, and PTIP. WDR5, RbBP5, ASH2L, and DPY30 form the four-subunit sub-complex WRAD, which is critical for H3K4 methyltransferase activity in all mammalian Set1-like histone methyltransferase complexes.[30] WDR5 binds directly with FYRN/FYRC domains of C-terminal SET domain-containing fragments of human KMT2C and KMT2D.[26] UTX, the complex’s H3K27 demethylase, PTIP, and PA1 are subunits that are unique to KMT2C and KMT2D.[26][31][32] KMT2D acts as a scaffold protein within the complex; absence of KMT2D results in destabilization of UTX and collapse of the complex in cells.[5][23]
Enhancer regulation
KMT2D is a major enhancer mono-methyltransferase and has partial functional redundancy with KMT2C.[5][7] The protein selectively binds enhancer regions based on type of cell and stage of differentiation. During differentiation, lineage determining transcription factors recruit KMT2D to establish cell-type specific enhancers. For example, CCAAT/enhancer-binding protein β (C/EBPβ), an early adipogenic transcription factor, recruits and requires KMT2D to establish a subset of adipogenic enhancers during adipogenesis. Depletion of KMT2D prior to differentiation prevents the accumulation of H3K4 mono-methylation (H3K4me1), H3K27 acetylation, the transcriptional coactivator Mediator, and RNA polymerase II on enhancers, resulting in severe defects in gene expression and cell differentiation.[5] KMT2C and KMT2D also identify super-enhancers and are required for formation of super-enhancers during cell differentiation.[33] Mechanistically, KMT2C and KMT2D are required for the binding of H3K27 acetyltransferases CREB-binding protein (CBP) and/or p300 on enhancers, enhancer activation, and enhancer-promotor looping prior to gene transcription.[5][33] The KMT2C and KMT2D proteins, rather than the KMT2C and KMT2D-mediated H3K4me1, control p300 recruitment to enhancers, enhancer activation, and transcription from promoters in embryonic stem cells.[7]
Functions
Development
Whole-body knockout of Kmt2d in mice results in early embryonic lethality.[5] Targeted knockout of Kmt2d in precursors cells of brown adipocytes and myocytes results in decreases in brown adipose tissue and muscle mass in mice, indicating that KMT2D is required for adipose and muscle tissue development.[5] In the hearts of mice, a single copy of the Kmt2d gene is sufficient for normal heart development.[34] Complete loss of Kmt2d in cardiac precursors and myocardium leads to severe cardiac defects and early embryonic lethality. KMT2D mediated mono- and di-methylation is required for maintaining necessary gene expression programs during heart development. Knockout studies in mice also show that KMT2D is required for proper B-cell development.[12]
Cell fate transition
KMT2D is partially functionally redundant with KMT2C and is required for cell differentiation in culture.[5][7] KMT2D regulates the induction of adipogenic and myogenic genes and is required for cell-type specific gene expression during differentiation. KMT2C and KMT2D are essential for adipogenesis and myogenesis.[5] Similar functions are seen in neuronal and osteoblast differentiation.[8][9] KMT2D facilitates cell fate transition by priming enhancers (through H3K4me1) for p300-mediated activation. For p300 to bind the enhancer, the physical presence of KMT2D, and not just the KMT2D-mediated H3K4me1, is required. However, KMT2D is dispensable for maintaining embryonic stem cell and somatic cell identity.[7]
Metabolism
KMT2D is partially functionally redundant with KMT2C in the liver as well. Heterozygous Kmt2d+/- mice exhibit enhanced glucose tolerance and insulin sensitivity and increased serum bile acid.[10] KMT2C and KMT2D are significant epigenetic regulators of the hepatic circadian clock and are co-activators of the circadian transcription factors retinoid-related orphan receptor (ROR)-α and -γ.[10] In mice, KMT2D also acts as a coactivator of PPARγ within the liver to direct over-nutrition induced steatosis. Heterozygous Kmt2d+/- mice exhibit resistance to over-nutrition induced hepatic steatosis.[11]
Tumor suppression
KMT2C and KMT2D along with NCOA6 act as coactivators of p53, a well-established tumor suppressor and transcription factor, and are necessary for endogenous expression of p53 in response to doxorubicin, a DNA damaging agent.[13] KMT2C and KMT2D have also been implicated with tumor suppressor roles in acute myeloid leukemia, follicular lymphoma, and diffuse large B cell lymphoma.[12][14][15] Knockout of Kmt2d in mice negatively affects the expression of tumor suppressor genes TNFAIP3, SOCS3, and TNFRSF14.[15]
Conversely, KMT2D deficiency in several breast and colon cancer cell lines leads to reduced proliferation.[35][36][37] Increased KMT2D was shown to facilitate chromatin opening and recruitment of transcription factors, including estrogen receptor (ER), in ER-positive breast cancer cells.[38] Thus, KMT2D may have diverse effects on tumor suppression in different cell types.
Clinical significance
Germline heterozygous loss of function mutations in KMT2D, also known as MLL2 in humans, cause
Germline heterozygous missense variants in exon 38 or 39 of the KMT2D gene cause another rare distinct multiple malformation disorder characterized by choanal atresia, athelia or hypoplastic nipples, branchial sinus abnormalities, neck pits, lacrimal duct anomalies, hearing loss, external ear malformations, and thyroid abnormalities.[17]
Congenital heart disease has been associated with an excess of mutations in genes that regulate H3K4 methylation, including KMT2D.[46]
Somatic frameshift and nonsense mutations in the SET and PHD domains affect 37% and 60%, respectively, of the total KMT2D mutations in cancers.[18] Cancers with somatic mutations in KMT2D occur most commonly in the brain, lymph nodes, blood, lungs, large intestine, and endometrium.[18] These cancers include medulloblastoma,[47][48][49] pheochromocytoma,[50] non-Hodgkin lymphomas,[51] cutaneous T-cell lymphoma, Sézary syndrome,[52] bladder, lung, and endometrial carcinomas,[53] esophageal squamous cell carcinoma,[54][55][56] pancreatic cancer,[57] and prostate cancer.[58]
Note
Wikidata Q39410059 . |
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000167548 - Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000048154 - Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ PMID 24368734.
- S2CID 31178216.
- ^ PMID 27698142.
- ^ PMID 23249737.
- ^ PMID 27732873.
- ^ PMID 25346535.
- ^ PMID 27806304.
- ^ PMID 26366712.
- ^ PMID 19433796.
- ^ PMID 24794707.
- ^ PMID 26366710.
- ^ PMID 20711175.
- ^ PMID 31949313.
- ^ PMID 25998713.
- ^ a b "Transcript: Kmt2d-001 (ENSMUST00000023741.15) - Summary - Mus musculus - Ensembl genome browser 88". www.ensembl.org.
- ^ a b "Transcript: KMT2D-001 (ENST00000301067.11) - Summary - Homo sapiens - Ensembl genome browser 88". www.ensembl.org.
- PMID 21875999.
- PMID 17218268.
- ^ PMID 28013028.
- PMID 28483418.
- PMID 12482968.
- ^ PMID 17500065.
- PMID 17178841.
- S2CID 23883131.
- PMID 18829457.
- PMID 22652693.
- PMID 22113294.
- PMID 18003914.
- ^ PMID 28398509.
- PMID 26932671.
- PMID 24240169.
- PMID 24491801.
- PMID 16603732.
- PMID 28336670.
- PMID 22126750.
- S2CID 204999137.
- S2CID 12327505.
- S2CID 7380692.
- S2CID 8316503.
- ^ "OMIM Entry - # 147920 - KABUKI SYNDROME 1; KABUK1". omim.org. Retrieved 2022-01-03.
- PMID 33674768.
- PMID 23665959.
- PMID 22820256.
- PMID 21163964.
- PMID 22832583.
- PMID 26032282.
- PMID 21796119.
- PMID 26551667.
- PMID 24132290.
- S2CID 32172173.
- PMID 24686850.
- S2CID 4467061.
- PMID 26154128.
- PMID 22722839.
External links
- GeneReviews/NCBI/NIH/UW entry on Kabuki syndrome, Kabuki Make-Up Syndrome, Niikawa-Kuroki Syndrome
- MLL2+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.