Citations for
1CDCA7, DNMT3B, HELLS, ICF1, ICF2, ICF3, ICF4, ZBTB24
CDCA7 and HELLS mutations undermine nonhomologous end joining in centromeric instability syndrome.
Unoki M, Funabiki H, Velasco G, Francastel C, Sasaki H.
J Clin Invest 129(1):78-92. doi: 10.1172/JCI99751. Epub 2018 Nov 19. 2019
2CDCA7, DNMT3B, HELLS, ICF1, ICF2, ICF3, ICF4, ZBTB24
Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features.
Alghamdi HA, Tashkandi SA, Alidrissi EM, Aledielah RD, AlSaidi KA, Alharbi ES, Habazi MK, Alzahrani MS.
J Clin Immunol 38(8):847-853. doi: 10.1007/s10875-018-0569-9. Epub 2018 Dec 3. No abstract available. 2018
3HELLS
HELLS regulates chromatin remodeling and epigenetic silencing of multiple tumor suppressor genes in human hepatocellular carcinoma.
Law CT, Wei L, Tsang FH, Chan CY, Xu IM, Lai RK, Ho DW, Lee JM, Wong CC, Ng IO, Wong CM.
Hepatology epatology. 2018 Dec 5. doi: 10.1002/hep.30414. [Epub ahead of print] 2018
4CDCA7, HELLS, ICF2, ICF3, ICF4, ZBTB24
Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state.
Velasco G, Grillo G, Touleimat N, Ferry L, Ivkovic I, Ribierre F, Deleuze JF, Chantalat S, Picard C, Francastel C.
Hum Mol Genet 27(14):2409-2424. doi: 10.1093/hmg/ddy130. 2018
5CDCA7, HELLS
HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome.
Jenness C, Giunta S, Müller MM, Kimura H, Muir TW, Funabiki H.
Proc Natl Acad Sci U S A 115(5):E876-E885. doi: 10.1073/pnas.1717509115. Epub 2018 Jan 16. 2018
6HELLS, POU5F1
Tethering of Lsh at the Oct4 locus promotes gene repression associated with epigenetic changes.
Ren J, Hathaway NA, Crabtree GR, Muegge K.
Epigenetics 13(2):173-181. doi: 10.1080/15592294.2017.1338234. Epub 2018 Feb 6. 2018
7HELLS
Lsh/HELLS regulates self-renewal/proliferation of neural stem/progenitor cells.
Han Y, Ren J, Lee E, Xu X, Yu W, Muegge K.
Sci Rep 7(1):1136. doi: 10.1038/s41598-017-00804-6. 2017
8DNMT3B, HELLS
The SNF2 family ATPase LSH promotes cell-autonomous de novo DNA methylation in somatic cells.
Termanis A, Torrea N, Culley J, Kerr A, Ramsahoye B, Stancheva I.
Nucleic Acids Res 44(16):7592-604. doi: 10.1093/nar/gkw424. Epub 2016 May 13. 2016
9CDCA7, HELLS, ICF3, ICF4
Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome.
Thijssen PE, Ito Y, Grillo G, Wang J, Velasco G, Nitta H, Unoki M, Yoshihara M, Suyama M, Sun Y, Lemmers RJ, de Greef JC, Gennery A, Picco P, Kloeckener-Gruissem B, Güngör T, Reisli I, Picard C, Kebaili K, Roquelaure B, Iwai T, Kondo I, Kubota T, van Ostaijen-Ten Dam MM, van Tol MJ, Weemaes C, Francastel C, van der Maarel SM, Sasaki H.
Nat Commun 6:7870. doi: 10.1038/ncomms8870. 2015
10HELLS
Genome-wide DNA methylation patterns in LSH mutant reveals de-repression of repeat elements and redundant epigenetic silencing pathways.
Yu W, McIntosh C, Lister R, Zhu I, Han Y, Ren J, Landsman D, Lee E, Briones V, Terashima M, Leighty R, Ecker JR, Muegge K.
Genome Res 24(10):1613-23. doi: 10.1101/gr.172015.114. Epub 2014 Aug 28. 2014
11E2F3, HELLS
The SNF2-like helicase HELLS mediates E2F3-dependent transcription and cellular transformation.
von Eyss B, Maaskola J, Memczak S, Möllmann K, Schuetz A, Loddenkemper C, Tanh MD, Otto A, Muegge K, Heinemann U, Rajewsky N, Ziebold U.
EMBO J 31(4):972-85. doi: 10.1038/emboj.2011.451. Epub 2011 Dec 13. 2012
12EHMT2, HELLS
LSH and G9a/GLP complex are required for developmentally programmed DNA methylation.
Myant K, Termanis A, Sundaram AY, Boe T, Li C, Merusi C, Burrage J, de Las Heras JI, Stancheva I.
Genome Res 21(1):83-94. Epub 2010 Dec 13. 2011
13E2F1, HELLS
Transcriptional activation of the senescence regulator Lsh by E2F1.
Niu J, Chen T, Han L, Wang P, Li N, Tong T.
Mech Ageing Dev 132(4):180-6. Epub 2011 Mar 29. 2011
14HELLS
Lsh mediated RNA polymerase II stalling at HoxC6 and HoxC8 involves DNA methylation.
Tao Y, Xi S, Briones V, Muegge K.
PLoS One 5(2):e9163. 2010
15HELLS
Senescence delay and repression of p16INK4a by Lsh via recruitment of histone deacetylases in human diploid fibroblasts.
Zhou R, Han L, Li G, Tong T.
Nucleic Acids Res 37(15):5183-96. Epub 2009 Jun 26. 2009
16HELLS
LSH cooperates with DNA methyltransferases to repress transcription.
Myant K, Stancheva I.
Mol Cell Biol 28(1):215-26. Epub 2007 Oct 29. 2008
17HELLS
Lsh controls Hox gene silencing during development.
Xi S, Zhu H, Xu H, Schmidtmann A, Geiman TM, Muegge K.
Proc Natl Acad Sci U S A 104(36):14366-71. Epub 2007 Aug 28. Erratum in: Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16389. 2007
18HELLS
Lsh is required for meiotic chromosome synapsis and retrotransposon silencing in female germ cells.
De La Fuente R, Baumann C, Fan T, Schmidtmann A, Dobrinski I, Muegge K.
Nat Cell Biol 8(12):1448-54. Epub 2006 Nov 19. 2006
19HELLS
Lsh, a modulator of CpG methylation, is crucial for normal histone methylation.
Yan Q, Huang J, Fan T, Zhu H, Muegge K.
EMBO J 22(19):5154-62. 2003
20HELLS
Characterization of gene expression, genomic structure, and chromosomal localization of Hells (Lsh).
Geiman TM, Durum SK, Muegge K.
Genomics 54 : 477-483. 1998