| Literature DB >> 27058938 |
Hu Wang1, Daojun Diao2, Zhencan Shi2, Xudong Zhu2, Yawei Gao3, Shaorong Gao3, Xiaoyu Liu3, You Wu3, K Lenhard Rudolph4, Guanghui Liu5, Tangliang Li2, Zhenyu Ju6.
Abstract
Proper regulation of Wnt signaling is critical for the maintenance of hematopoietic stem cell (HSC) homeostasis. The epigenetic regulation of Wnt signaling in HSCs remains largely unknown. Here, we report that the histone deacetylase SIRT6 regulates HSC homeostasis through the transcriptional repression of Wnt target genes. Sirt6 deletion promoted HSC proliferation through aberrant activation of Wnt signaling. SIRT6-deficient HSCs exhibited impaired self-renewal ability in serial competitive transplantation assay. Mechanistically, SIRT6 inhibits the transcription of Wnt target genes by interacting with transcription factor LEF1 and deacetylating histone 3 at lysine 56. Pharmacological inhibition of the Wnt pathway rescued the aberrant proliferation and functional defect in SIRT6-deficient HSCs. Taken together, these findings disclose a new link between SIRT6 and Wnt signaling in the regulation of adult stem cell homeostasis and self-renewal capacity.Entities:
Keywords: SIRT6; Wnt; epigenetic modification; hematopoietic stem cell
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Year: 2016 PMID: 27058938 DOI: 10.1016/j.stem.2016.03.005
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633