Citations for
1ESCO1, ESCO2, MMS22L
Cul4-Ddb1 ubiquitin ligases facilitate DNA replication-coupled sister chromatid cohesion through regulation of cohesin acetyltransferase Esco2.
Sun H, Zhang J, Xin S, Jiang M, Zhang J, Li Z, Cao Q, Lou H.
PLoS Genet 15(2):e1007685. doi: 10.1371/journal.pgen.1007685. eCollection 2019 Feb. 2019
2ESCO2, RBS
Stimulation of mTORC1 with L-leucine rescues defects associated with Roberts syndrome.
Xu B, Lee KK, Zhang L, Gerton JL.
PLoS Genet 9(10):e1003857. doi: 10.1371/journal.pgen.1003857. Epub 2013 Oct 3. 2013
3ESCO2
Localization and regulation of murine Esco2 during male and female meiosis.
Evans EB, Hogarth C, Evanoff RM, Mitchell D, Small C, Griswold MD.
Biol Reprod 87(3):61. doi: 10.1095/biolreprod.112.099978. Print 2012 Sep. 2012
4ESCO1, ESCO2, RBS
The non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions.
Whelan G, Kreidl E, Peters JM, Eichele G.
Nucleus 3(4):330-4. Epub 2012 May 22. Review. 2012
5ESCO2
Esco2 promotes neuronal differentiation by repressing Notch signaling.
Leem YE, Choi HK, Jung SY, Kim BJ, Lee KY, Yoon K, Qin J, Kang JS, Kim ST.
Cell Signal 23(11):1876-84. doi: 10.1016/j.cellsig.2011.07.006. Epub 2011 Jul 14. 2011
6ESCO2, ZNF143
Transcriptional regulation of the human establishment of cohesion 1 homolog 2 gene.
Nishihara M, Yamada M, Nozaki M, Nakahira K, Yanagihara I.
Biochem Biophys Res Commun 393(1):111-7. Epub 2010 Jan 29. 2010
7ESCO2, RBS
The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2.
van der Lelij P, Godthelp BC, van Zon W, van Gosliga D, Oostra AB, Steltenpool J, de Groot J, Scheper RJ, Wolthuis RM, Waisfisz Q, Darroudi F, Joenje H, de Winter JP.
PLoS One 4(9):e6936.PMID: 19738907 2009
8ESCO1, ESCO2
Cohesin acetylation speeds the replication fork.
Terret ME, Sherwood R, Rahman S, Qin J, Jallepalli PV.
Nature 462(7270):231-4.PMID: 19907496 2009
9ESCO2, EHMT2, SETDB1, SUV39H1
Esco2 is a novel corepressor that associates with various chromatin modifying enzymes.
Kim BJ, Kang KM, Jung SY, Choi HK, Seo JH, Chae JH, Cho EJ, Youn HD, Qin J, Kim ST.
Biochem Biophys Res Commun 372(2):298-304. Epub 2008 May 21. 2008
10ESCO2, RBS
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
Gordillo M, Vega H, Trainer AH, Hou F, Sakai N, Luque R, Kayserili H, Basaran S, Skovby F, Hennekam RC, Uzielli ML, Schnur RE, Manouvrier S, Chang S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Schultz RA, McDaniel LD, Ozono K, Inui K, Zou H, Jabs EW.
Hum Mol Genet 17(14):2172-80. Epub 2008 Apr 14. 2008
11ESCO2, RBS
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.
Vega H, Waisfisz Q, Gordillo M, Sakai N, Yanagihara I, Yamada M, van Gosliga D, Kayserili H, Xu C, Ozono K, Wang Jabs E, Inui K, Joenje H.
Nat Genet 37(5):468-70. Epub 2005 Apr 10. 2005
12RBS, ESCO2
Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells.
McDaniel LD, Tomkins DJ, Stanbridge EJ, Somerville MJ, Friedberg EC, Schultz RA.
Am J Hum Genet 77(1):132-9. Epub 2005 May 10. 2005
13ESCO2, RBS
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.
Schule B, Oviedo A, Johnston K, Pai S, Francke U.
Am J Hum Genet 77(6):1117-28. Epub 2005 Oct 31. 2005