| Literature DB >> 29378332 |
Shan-He Yu1, Kang-Yong Zhu2, Fan Zhang3, Juan Wang4, Hao Yuan5, Yi Chen3, Yi Jin3, Mei Dong2, Lei Wang2, Xiao-E Jia2, Lei Gao2, Zhi-Wei Dong2, Chun-Guang Ren2, Li-Ting Chen6, Qiu-Hua Huang3, Min Deng2, Leonard I Zon7, Yi Zhou7, Jiang Zhu8, Peng-Fei Xu9, Ting-Xi Liu10.
Abstract
The histone demethylase Jmjd3 plays a critical role in cell lineage specification and differentiation at various stages of development. However, its function during normal myeloid development remains poorly understood. Here, we carried out a systematic in vivo screen of epigenetic factors for their function in hematopoiesis and identified Jmjd3 as a new epigenetic factor that regulates myelopoiesis in zebrafish. We demonstrated that jmjd3 was essential for zebrafish primitive and definitive myelopoiesis, knockdown of jmjd3 suppressed the myeloid commitment and enhanced the erythroid commitment. Only overexpression of spi1 but not the other myeloid regulators rescued the myeloid development in jmjd3 morphants. Furthermore, preliminary mechanistic studies demonstrated that Jmjd3 could directly bind to the spi1 regulatory region to alleviate the repressive H3K27me3 modification and activate spi1 expression. Thus, our studies highlight that Jmjd3 is indispensable for early zebrafish myeloid development by promoting spi1 expression.Entities:
Keywords: Histone demethylase; Jmjd3; Myelopoiesis; Spi1; Zebrafish
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Year: 2018 PMID: 29378332 PMCID: PMC5972518 DOI: 10.1016/j.bbagrm.2017.12.009
Source DB: PubMed Journal: Biochim Biophys Acta Gene Regul Mech ISSN: 1874-9399 Impact factor: 4.490