Trowbridge Jennifer J, Snow Jonathan W, Kim Jonghwan, Orkin Stuart H
Department of Pediatric Oncology, Dana-Farber Cancer Institute and Division of Hematology/Oncology, Children's Hospital Boston, Harvard Stem Cell Institute, Harvard Medical School, Boston, MA 02115, USA.
Cell Stem Cell. 2009 Oct 2;5(4):442-9. doi: 10.1016/j.stem.2009.08.016.
DNA methylation is essential for development and in diverse biological processes. The DNA methyltransferase Dnmt1 maintains parental cell methylation patterns on daughter DNA strands in mitotic cells; however, the precise role of Dnmt1 in regulation of quiescent adult stem cells is not known. To examine the role of Dnmt1 in adult hematopoietic stem cells (HSCs), we conditionally disrupted Dnmt1 in the hematopoietic system. Defects were observed in Dnmt1-deficient HSC self-renewal, niche retention, and in the ability of Dnmt1-deficient HSCs to give rise to multilineage hematopoiesis. Loss of Dnmt1 also had specific impact on myeloid progenitor cells, causing enhanced cell cycling and inappropriate expression of mature lineage genes. Dnmt1 regulates distinct patterns of methylation and expression of discrete gene families in long-term HSCs and multipotent and lineage-restricted progenitors, suggesting that Dnmt1 differentially controls these populations. These findings establish a unique and critical role for Dnmt1 in the primitive hematopoietic compartment.
DNA甲基化对于发育及多种生物学过程至关重要。DNA甲基转移酶Dnmt1在有丝分裂细胞中维持子代DNA链上的亲代细胞甲基化模式;然而,Dnmt1在静息成年干细胞调控中的精确作用尚不清楚。为了研究Dnmt1在成年造血干细胞(HSC)中的作用,我们在造血系统中条件性地破坏Dnmt1。在缺乏Dnmt1的HSC自我更新、龛位保留以及缺乏Dnmt1的HSC产生多谱系造血的能力方面观察到缺陷。Dnmt1的缺失对髓系祖细胞也有特定影响,导致细胞周期增强以及成熟谱系基因的不适当表达。Dnmt1在长期HSC以及多能和谱系受限祖细胞中调控不同的甲基化模式和离散基因家族的表达,表明Dnmt1以不同方式控制这些细胞群体。这些发现确立了Dnmt1在原始造血区室中的独特且关键的作用。