H3K9me3-heterochromatin loss at protein-coding genes enables developmental lineage specification

Author:

Nicetto Dario123ORCID,Donahue Greg123,Jain Tanya123,Peng Tao45,Sidoli Simone26ORCID,Sheng Lihong23ORCID,Montavon Thomas7ORCID,Becker Justin S.123ORCID,Grindheim Jessica M.123,Blahnik Kimberly123,Garcia Benjamin A.26,Tan Kai3458,Bonasio Roberto23ORCID,Jenuwein Thomas7,Zaret Kenneth S.123ORCID

Affiliation:

1. Institute for Regenerative Medicine, University of Pennsylvania, Philadelphia, PA, USA.

2. Penn Epigenetics Institute, University of Pennsylvania, Philadelphia, PA, USA.

3. Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA, USA.

4. Department of Biomedical and Health Informatics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA.

5. Division of Oncology and Center for Childhood Cancer Research, Children’s Hospital of Philadelphia, Philadelphia, PA, USA.

6. Department of Biochemistry and Molecular Biophysics, University of Pennsylvania, Philadelphia, PA, USA.

7. Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.

8. Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Abstract

Reversing chromatin dynamics for development Compacted chromatin regions, marked by trimethylation of histone H3 at position lysine 9 (H3K9me3), occur at highly repeated DNA sequences, helping to suppress recombination and gene expression. Because pluripotent cells contain low levels of H3K9me3 heterochromatin relative to differentiated cells, it has been thought that an increase in such heterochromatin helps to define cell differentiation. Nicetto et al. used two independent methods to examine compacted heterochromatic domains and found that H3K9me3 compaction increased at protein-coding genes during early mouse organogenesis. During differentiation, these domains open up to allow cell-specific expression. Loss of heterochromatin by genetic inactivation of the H3K9me3 methyltransferases caused ectopic expression of cell-inappropriate genes and tissue pathology. Science , this issue p. 294

Funder

NIH Office of the Director

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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