Chromocentres and pericentromeric satellite heterochromatin — no KMT2A evidence, but the AT-hook argument says there should be
also called chromocenter · pericentromeric heterochromatin · satellite DNA · HMGA1 chromocentre · D1 satellite bundling
Chromocentres are dense clumps where the AT-rich repetitive DNA near chromosome centres from different chromosomes bundles together. Other proteins with the same DNA-gripping hooks as KMT2A pile up there and hold the clumps together — but nobody has ever reported KMT2A or its fusions at a chromocentre, and that silence is itself informative.
The same thing, for a scientist
Direct evidence for KMT2A or any KMT2A fusion at chromocentres, pericentromeric or satellite heterochromatin: **none**. Searches for MLL AND pericentromeric heterochromatin, KMT2A AND satellite heterochromatin, and MLL AND chromocenter each returned zero relevant primary studies. The indirect argument, however, is unusually strong and points the other way. Jagannathan, Cummings & Yamashita showed that **multi-AT-hook satellite-DNA-binding proteins — Drosophila D1 and mouse HMGA1 — bundle pericentromeric satellite DNA from heterologous chromosomes into chromocentres**, and that loss of this function causes micronucleation, DNA damage and cell death; they propose this as a conserved function for pericentromeric satellite DNA [E1]. KMT2A carries three AT-hooks (169-180, 217-227, 301-309) [E2] and is therefore a multi-AT-hook nuclear protein of exactly that class. Its absence from chromocentres needs explaining rather than merely noting, and there is a candidate explanation already in this graph: the only direct assay of MLL's own AT-hooks reported binding to **cruciform DNA — structure rather than sequence** [E3], not to AT-rich sequence. A structure-selective tether would not concentrate at AT-rich satellite. If that is right, the chromocentre negative is a prediction confirmed rather than an oversight, and it is the best available independent evidence that MLL's hooks are not conventional AT-sequence readers.
What chromocentres are and why an AT-hook protein should be there1 deeper
Pericentromeric satellite DNA is highly repetitive and AT-rich. Jagannathan et al. found that in Drosophila the multi-AT-hook protein D1 and in mouse cells HMGA1 bind satellite DNA and bundle it from heterologous chromosomes into chromocentres; disrupting this causes micronuclei, DNA damage and death, which is why they argue satellite DNA has a conserved function rather than being junk 1. The mechanism is explicitly multivalency: several AT-hooks on one polypeptide cross-link several satellite arrays.
KMT2A has three AT-hooks in a 140-residue stretch. Structurally it belongs to the same class. HMGA1 and KMT2A are both abundant nuclear AT-hook proteins expressed in haematopoietic cells. There is no a-priori reason KMT2A should be excluded from satellite DNA on motif grounds alone.
Three possible reasons for the negative, with different consequences
(a) Nobody looked. Plausible: chromocentres are not on anyone's KMT2A hypothesis list, and the standard anti-MLL immunofluorescence images were read for 'punctate nucleoplasm' without scoring DAPI-dense foci. A DAPI-dense-focus overlap score on any existing image set is a zero-cost test.
(b) The hooks are structure-selective, not AT-selective. The 1994 EMSA on the MLL AT-hook region reported cruciform binding and explicitly 'structure rather than sequence' 3. Cruciform extrusion requires inverted repeats under supercoiling; monotonous satellite arrays are not the obvious substrate. On this reading the negative is real and expected.
(c) Occupancy is competed away. HMGA1 is present at very high copy number and binds AT-rich DNA avidly. Even an AT-competent KMT2A would lose the competition at satellite while winning at CpG islands, where HMGA1 has no advantage and CXXC does. This predicts that HMGA1 depletion would reveal KMT2A at chromocentres — a one-experiment discriminator between (b) and (c).
Option (b) is the one this graph currently favours, because it also explains the nuclear-matrix/SAR association recorded elsewhere in the beat.
Why this matters beyond bookkeeping
Chromocentre integrity is a genome-stability function: losing the bundling protein produces micronuclei and DNA damage 1. KMT2A-rearranged infant leukemia is the classic quiet genome — very low mutation burden, essentially one driver lesion. If KMT2A had a chromocentre-maintenance role, its heterozygous disruption by the translocation would predict genome instability, and the disease's defining feature is the opposite. The absence of KMT2A from chromocentres is therefore concordant with the low-mutation-burden phenotype recorded in comut-low-mutation-burden-infant-kmt2a-r, and a positive finding here would sit awkwardly with it. That consistency is worth recording, because it means the negative is not merely an unexamined corner: it fits.
| compartment | chromocentre / pericentromeric satellite heterochromatin |
|---|---|
| evidence class for kmt2a | none direct; indirect motif-class argument points toward presence, direct MLL binding data point away |
| direct evidence | false |
| indirect evidence via partner | false |
| indirect evidence via motif class | true |
marker proteins
[ "HP1 alpha (CBX5)", "H3K9me3", "DAPI-dense foci", "SUV39H1" ]
searches returning zero
[ "MLL AND pericentromeric heterochromatin", "KMT2A AND satellite heterochromatin", "MLL AND chromocenter", "HMGA2 AT-rich heterochromatin localization" ]
- Any drug designed against the AT-hook-DNA interaction risks hitting HMGA1's chromocentre-bundling function, whose loss causes micronucleation and DNA damage — a genotoxicity that would be unacceptable in infants and would not show up in short-term cell-viability screens.
- If KMT2A does contribute to chromocentre organisation in some cell states and this has been missed, then degrading the fusion could destabilise pericentromeric heterochromatin in the surviving normal cells that also carry the wild-type allele — a class of toxicity nobody is monitoring.
- Score DAPI-dense-focus overlap on any existing endogenous KMT2A immunofluorescence image set. If KMT2A is excluded from chromocentres, that is independent evidence its AT-hooks are not AT-sequence readers, and it costs nothing.
- Does HMGA1 depletion reveal KMT2A at chromocentres? This discriminates 'structurally incapable' from 'competed away' and is a single knockdown plus a co-stain.
- Is there any satellite-derived transcript signature in KMT2A-rearranged blasts? Satellite derepression is a general cancer phenomenon; its absence in a quiet-genome leukemia would be worth documenting either way and is a free reanalysis of existing RNA-seq.
- Does the fusion's three-AT-hook multivalency contribute avidity at its real targets in a way a single hook would not? The triple-alanine mutant proposed in the AT-hook entry answers this and the chromocentre question at the same time.
- E1strong confidence 4 of 5: Replicated in peer-reviewed work by more than one group.paper
Multi-AT-hook satellite-DNA-binding proteins — Drosophila D1 and mouse HMGA1 — bundle pericentromeric satellite DNA from heterologous chromosomes into chromocentres, and loss of this function causes micronucleation, DNA damage and cell death, indicating a conserved function for pericentromeric satellite DNA.
A conserved function for pericentromeric satellite DNA · Jagannathan M, Cummings R, Yamashita YM · eLife 2018What this evidence cannot show
Drosophila and mouse cells; no human data and no haematopoietic cells. The bundling function is demonstrated for D1 and HMGA1, and transfer of the property to any other multi-AT-hook protein is an inference the authors do not make.
Evidence that argues against this (1)
- The analogy from multi-AT-hook satellite bundlers to KMT2A fails at the point where it would have to predict localisation. Yano et al. mapped the determinants of MLL/ALL-1 punctate subnuclear distribution to two short TRITHORAX-conserved elements in the N-terminal region, not to the AT hooks, and interpreted the resulting speckles as complexes of ALL-1 positioned at its TARGET SITES ON CHROMATIN - euchromatic target genes - rather than at heterochromatin. Drosophila D1 and mouse HMGA1 carry roughly ten or more AT hooks and bundle satellite; KMT2A carries three, and its punctate pattern is accounted for by elements that are not the hooks. Read: abstract only. Yano T et al. 1997
- E2established confidence 5 of 5: Multiple independent lines of evidence; treated as settled in the field.database
Human KMT2A carries three annotated A.T hook motifs at residues 169-180, 217-227 and 301-309, placing it structurally in the multi-AT-hook protein class.
UniProtKB Q03164 (KMT2A_HUMAN) — Histone-lysine N-methyltransferase 2A · UniProt Consortium · UniProt Knowledgebase 2026What this evidence cannot show
Motif-matched curated annotation; membership of a motif class does not entail shared binding behaviour, which is precisely the point at issue here.
Evidence that argues against this (1)
- Searched and empty, recorded explicitly, and this is the honest state of the entry. No published study localises KMT2A, any KMT2A fusion, or the MLL N-terminal fragment to chromocentres, pericentromeric heterochromatin or satellite DNA, in any species. PubMed searches on 2026-09-18 combining MLL/KMT2A/ALL-1 with pericentromeric, chromocentre/chromocenter, satellite DNA, major satellite, HP1 and constitutive heterochromatin returned nothing. The `weak` grade is therefore generous rather than harsh: the entry records a structural analogy with no observation behind it, and should be read as a hypothesis for a two-colour FISH/immunofluorescence experiment rather than as a localisation claim. No citation is attached because there is nothing to cite: this note is a bounded absence recording searches that returned nothing, not a sourced fact. Uncited and unciteable look identical in this field, so it is said here explicitly (Q42 citation-integrity repair, 2026-09-20).
- E3moderate confidence 3 of 5: One strong study, or several smaller consistent ones.paper
The MLL AT-hook region binds cruciform DNA and recognises the structure rather than the sequence of the target DNA, which would not predict accumulation on monotonous AT-rich satellite arrays.
11q23 translocations split the 'AT-hook' cruciform DNA-binding region and the transcriptional repression domain from the activation domain of the mixed-lineage leukemia (MLL) gene · Zeleznik-Le NJ, Harden AM, Rowley JD · Proceedings of the National Academy of Sciences USA 1994What this evidence cannot show
A 1994 gel-shift with a limited probe panel on a bacterially expressed fragment; the inference that this predicts absence from satellite DNA is the graph's, not the paper's, and has never been tested.
Evidence that argues against this (1)
- The inference runs the wrong way once the structure is read. This item argues that structure-reading (cruciform) binding predicts absence from monotonous AT-rich satellite arrays - but the protein whose AT-hooks define the motif, HMG-I(Y)/HMGA1, is one of the two multi-AT-hook satellite-bundling proteins in the chromocentre result this entry cites, and Huth et al. show its binding to ordinary B-form AT-rich duplex is exactly a structural function: a central Arg-Gly-Arg plus two accessory modules, one protein bridging two DNA molecules, stabilising B-DNA rather than recognising an unusual conformation. Structure-reading and satellite binding are therefore not alternatives, and a one-to-two protein-to-DNA stoichiometry is a bundling architecture. The 1994 cruciform result does not predict KMT2A's absence from chromocentres; the prediction is the graph's own and remains untested. Huth JR et al. 1997
Searched and empty: no study places KMT2A or any KMT2A fusion at chromocentres or pericentromeric satellite in any species, and MLL's punctate determinants are the SNL elements rather than the AT hooks
the chromocentre negative is a prediction of structure-selective rather than AT-selective hooks
absence from chromocentres is concordant with the quiet-genome phenotype
G9a writes the EUCHROMATIC H3K9 methylation, explicitly in contrast to pericentromeric heterochromatin
DEK loss drives H3.3 into pericentric heterochromatin and reduces heterochromatin globally
DAXX's second address is condensed chromatin, entered at the end of S phase and vacated in early G2
KDM4C's only published subnuclear placement is heterochromatin, which conflicts with this graph's active-target-gene model
the heterochromatin community HRP2 sits in - HP1alpha and MPP8/HUSH - is the same protein set that defines this graph's pericentromeric compartment; HRP2 has never been imaged there in a KMT2A-rearranged cell
BMI1 with RING1 and hPc2 associates tightly with pericentromeric heterochromatin at 1q12 and related sequences, and the association is retained through mitosis - the strongest pericentromeric assignment in this graph, made in fibroblasts
RAD21 persists at metaphase centromeres after leaving chromosome arms at prophase - a stage-resolved, mitotic address, not an interphase one
SA2 is required for CENTROMERE cohesion while SA1 is required for TELOMERE cohesion - the two mutually exclusive rings partition the genome by subnuclear region
PcG bodies are described as located on regions of pericentric heterochromatin (PMID 16314526)
- ← related toEED - the PRC2 subunit this disease actually needs, with drugs in the clinic and zero leukaemia studies
PcG bodies, whose formation EED licenses, are located on regions of pericentric heterochromatin (PMID 16314526)
H2A.Z is a structural component of the centromere and is distributed nonuniformly through pericentric heterochromatin (PMID 17194760)
CTCF binds unusual pericentric/centromeric sites through its C-terminal fingers EARLY IN MITOSIS and recruits CENP-E (PMID 26321640); the position is cell-cycle-scoped, so a single-state localisation record for CTCF would be wrong (Q89 2026-09-21)
first pan-fusion interactor with a documented chromocentre address: direct pericentric DNA binding and de novo H3K9 methylation via SUV39H1/2 (Ma 2024), chromocentre imaging by CasID (Schmidtmann 2016)
The one heterochromatin-adjacent EP400 claim is WEAK and points against the pathway's main function: TIP60/P400/H4K12ac proposed as a heterochromatin back-up skeleton in 77 breast tumours, on ChIP-reChIP co-occupancy (PMID 33099470), while EP400's established job is depositing H2A.Z at active and regulatory chromatin (Q93 2026-09-21)
FULL-LENGTH DNMT3A IS CONCENTRATED ON HETEROCHROMATIN and accumulates in the MAJOR SATELLITE REPEATS at pericentric heterochromatin, while the DNMT3A2 isoform - lacking the N-terminal 223 residues, from a downstream intronic promoter - is EUCHROMATIC (PMID 12138111). A positive, isoform-resolved subnuclear assignment; never measured in a leukaemic cell (Q93 2026-09-21)
BRD3's only named subnuclear compartment, stress-conditional and NOT paralogue-resolved: heat shock makes HSF1 recruit GCN5, TIP60 and p300 to pericentric heterochromatin, and the resulting hyperacetylation recruits BRD2, BRD3 and BRD4, all required for satellite III transcription (PMID 28710461). A normally H3K9me-dense compartment BET proteins avoid becomes accessible once it acquires the acetyl mark (Q95 2026-09-22)
SINGLE-SOURCE, 2026, and SWI/SNF-INDEPENDENT: ARID1A interacts with TRIM28 to preserve heterochromatin rigidity outside the SWI/SNF complex, and its loss displaces SETDB1, reversing H3K9me3 repression at endogenous retroelements and triggering viral mimicry (PMID 41661654, colorectal cancer). One group, one disease - recorded as single-source, not established. TRIM28 is not TRIM27 (Q95 2026-09-22)
the HMG-I(Y) structure (one protein bridging two duplexes) makes satellite bundling and 'structure reading' the same activity, not alternatives