Deletion of the XIST promoter from the human inactive X chromosome compromises polycomb heterochromatin maintenance
Author:
Funder
National Institute of General Medical Sciences
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00412-021-00754-z.pdf
Reference92 articles.
1. Adrianse RL et al (2018) Perturbed maintenance of transcriptional repression on the inactive X-chromosome in the mouse brain after Xist deletion. Epigenetics Chromatin 11:50. https://doi.org/10.1186/s13072-018-0219-8
2. Arzate-Mejia RG, Recillas-Targa F, Corces VG (2018) Developing in 3D: the role of CTCF in cell differentiation. Development 145:dev137729. https://doi.org/10.1242/dev.137729
3. Bannister AJ, Zegerman P, Partridge JF, Miska EA, Thomas JO, Allshire RC, Kouzarides T (2001) Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain. Nature 410:120–124
4. Barr ML, Bertram EG (1949) A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis. Nature 163:676–677
5. Baumann C, De La Fuente R (2009) ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells. Chromosoma 118:209–222. https://doi.org/10.1007/s00412-008-0189-x
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