Gao Guozhen, Dornelas Moreira Josimar, Das Prosun, Lin Kevin, Ge Kai, Chen Taiping, Lu Yue, Santos Margarida A
Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Biochemistry, Sapthagiri Institute of Medical Sciences & Research Centre, Sapthagiri NPS University, Bangalore, India.
Nat Commun. 2025 Jul 1;16(1):5737. doi: 10.1038/s41467-025-61247-6.
Circulating blood platelets are responsible for maintaining hemostasis. They are released into blood vessels from mature megakaryocytes. Although several transcription factors have been reported to orchestrate the transcriptional programs required for platelet production, how chromatin regulators control these processes is still poorly understood. MLL3 and MLL4 are the main lysine methyltransferases responsible for the deposition of H3K4me1 histone marks at enhancers. MLL3 and MLL4 typically form complexes with other co-factors, such as PTIP. Recently, we showed that loss of PTIP leads to decreased platelet numbers in mice. Here, we find that, although MLL3/4 double deficiency does not alter megakaryopoiesis and endomitosis, the final step of megakaryocyte maturation is affected due to an abnormal cytoskeleton and demarcation membrane system. MLL3/4 double-deficient mice develop macrothrombocytopenia; platelets are preactive and pro-apoptotic, leading to their rapid clearance from the circulation. Increased megakaryopoeisis in the bone marrow and spleen cannot compensate for these abnormalities. Mechanistically, the expression of genes responsible for normal megakaryocyte function and platelet production is altered in MLL3/4-deficient megakaryocytes, partly due to impaired enhancer functions associated with these genes. Our findings provide insights into the epigenetic programs that are important for platelet biogenesis.
循环血液中的血小板负责维持止血功能。它们从成熟的巨核细胞释放到血管中。尽管已有报道称几种转录因子可协调血小板生成所需的转录程序,但染色质调节因子如何控制这些过程仍知之甚少。MLL3和MLL4是主要的赖氨酸甲基转移酶,负责在增强子处沉积H3K4me1组蛋白标记。MLL3和MLL4通常与其他辅助因子形成复合物,如PTIP。最近,我们发现PTIP缺失会导致小鼠血小板数量减少。在此,我们发现,尽管MLL3/4双缺失不会改变巨核细胞生成和核内有丝分裂,但由于异常的细胞骨架和分界膜系统,巨核细胞成熟的最后一步受到影响。MLL3/4双缺失小鼠会出现大血小板减少症;血小板处于预激活状态且促凋亡,导致它们从循环中快速清除。骨髓和脾脏中巨核细胞生成增加并不能弥补这些异常。从机制上讲,负责正常巨核细胞功能和血小板生成的基因表达在MLL3/4缺陷的巨核细胞中发生改变,部分原因是与这些基因相关的增强子功能受损。我们的研究结果为对血小板生物发生至关重要的表观遗传程序提供了见解。