H4K20me1 and H3K27me3 are concurrently loaded onto the inactive X chromosome but dispensable for inducing gene silencing-Reference-Cited by-同舟云学术

H4K20me1 and H3K27me3 are concurrently loaded onto the inactive X chromosome but dispensable for inducing gene silencing

Published:2021-02-19 Issue:3 Volume:22 Page:
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Tjalsma Sjoerd J D¹,Hori Mayako²,Sato Yuko²³^ORCID,Bousard Aurelie¹,Ohi Akito²,Raposo Ana Cláudia⁴,Roensch Julia¹,Le Saux Agnes¹,Nogami Jumpei⁵,Maehara Kazumitsu⁵^ORCID,Kujirai Tomoya⁶,Handa Tetsuya³^ORCID,Bagés‐Arnal Sandra⁷,Ohkawa Yasuyuki⁵^ORCID,Kurumizaka Hitoshi⁶,da Rocha Simão Teixeira⁴^ORCID,Żylicz Jan J¹⁷⁸^ORCID,Kimura Hiroshi²³^ORCID,Heard Edith⁹¹⁰^ORCID

Affiliation:

1. Mammalian Developmental Epigenetics Group Institut Curie CNRS UMR3215, INSERM U934PSL University Paris France

2. Graduate School of Bioscience and Biotechnology Tokyo Institute of Technology Yokohama Japan

3. Cell Biology Center Institute of Innovative Research Tokyo Institute of Technology Yokohama Japan

4. Faculdade de Medicina Instituto de Medicina MolecularJoão Lobo AntunesUniversidade de Lisboa Lisboa Portugal

5. Division of Transcriptomics Medical Institute of BioregulationKyushu University Fukuoka Japan

6. Institute for Quantitative Biosciences The University of Tokyo Tokyo Japan

7. The Novo Nordisk Foundation Center for Stem Cell Biology Copenhagen Denmark

8. Department of Physiology Development and Neuroscience University of Cambridge Cambridge UK

9. EMBL Heidelberg Heidelberg Germany

10. Collège de France Paris France

Funder

Fundação para a Ciência e a Tecnologia

Fundo Regional para a Ciência e Tecnologia

H2020 European Research Council

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Novo Nordisk Fonden

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embr.202051989

Reference73 articles.

1. Nonhistone nuclear proteins specific to certain mouse embryonal carcinoma clones having an inactive X chromosome*1

2. PCGF3/5–PRC1 initiates Polycomb recruitment in X chromosome inactivation

3. Visualization of specific DNA sequences in living mouse embryonic stem cells with a programmable fluorescent CRISPR/Cas system

4. Reduction in chromosome mobility accompanies nuclear organization during early embryogenesis in Caenorhabditis elegans

5. PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription

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