Histone H3K4 methylation-dependent and -independent functions of Set1A/COMPASS in embryonic stem cell self-renewal and differentiation

• Published in: Genes & development Vol. 31; no. 17; pp. 1732 - 1737
• Main Authors: Sze, Christie C, Cao, Kaixiang, Collings, Clayton K, Marshall, Stacy A, Rendleman, Emily J, Ozark, Patrick A, Chen, Fei Xavier, Morgan, Marc A, Wang, Lu, Shilatifard, Ali
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 01-09-2017
• Subjects: Animals; Cell Differentiation - genetics; Cell Proliferation - genetics; Embryonic Stem Cells - cytology; Embryonic Stem Cells - enzymology; Gene Deletion; Gene Expression Regulation, Developmental - genetics; Histone-Lysine N-Methyltransferase - genetics; Histone-Lysine N-Methyltransferase - metabolism; Histones - metabolism; Methylation; Mice; Myeloid-Lymphoid Leukemia Protein - metabolism; PR-SET Domains - genetics; Research Communication; COMPASS; H3K4 methylation; Set1A; differentiation; pluripotency; self-renewal
• ISSN: 0890-9369; 1549-5477
• DOI: 10.1101/gad.303768.117

Of the six members of the COMPASS (complex of proteins associated with Set1) family of histone H3 Lys4 (H3K4) methyltransferases identified in mammals, Set1A has been shown to be essential for early embryonic development and the maintenance of embryonic stem cell (ESC) self-renewal. Like its familial relatives, Set1A possesses a catalytic SET domain responsible for histone H3K4 methylation. Whether H3K4 methylation by Set1A/COMPASS is required for ESC maintenance and during differentiation has not yet been addressed. Here, we generated ESCs harboring the deletion of the SET domain of Set1A (Set1A
); surprisingly, the Set1A SET domain is dispensable for ESC proliferation and self-renewal. The removal of the Set1A SET domain does not diminish bulk H3K4 methylation in ESCs; instead, only a subset of genomic loci exhibited reduction in H3K4me3 in Set1A
cells, suggesting a role for Set1A independent of its catalytic domain in ESC self-renewal. However, Set1A
ESCs are unable to undergo normal differentiation, indicating the importance of Set1A-dependent H3K4 methylation during differentiation. Our data also indicate that during differentiation, Set1A but not Mll2 functions as the H3K4 methylase on bivalent genes and is required for their expression, supporting a model for transcriptional switch between Mll2 and Set1A during the self-renewing-to-differentiation transition. Together, our study implicates a critical role for Set1A catalytic methyltransferase activity in regulating ESC differentiation but not self-renewal and suggests the existence of context-specific H3K4 methylation that regulates transcriptional outputs during ESC pluripotency.