...
首页> 外文期刊>Blood: The Journal of the American Society of Hematology >The KDM4/JMJD2 histone demethylases are required for hematopoietic stem cell maintenance
【24h】

The KDM4/JMJD2 histone demethylases are required for hematopoietic stem cell maintenance

机译:造血干细胞维持需要KDM4 / JMJD2组蛋白去甲基酶

获取原文
获取原文并翻译 | 示例

摘要

KDM4/JMJD2 are H3K9-and H3K36-specific demethylases, which are considered promising therapeutic targets for the treatment of acute myeloid leukemia (AML) harboring MLL translocations. Here, we investigate the long-term effects of depleting KDM4 activity on normal hematopoiesis to probe potential side effects of continuous inhibition of these enzymes. Utilizing conditional Kdm4a/Kdm4b/Kdm4c triple-knockout mice, we show that KDM4 activity is required for hematopoietic stem cell (HSC) maintenance in vivo. The knockout of the KDM4 demethylases leads to accumulation of H3K9me3 on transcription start sites and the corresponding downregulation of expression of several genes in HSCs. We show that 2 of these genes, Taf1b and Nom1, are essential for the maintenance of hematopoietic cells. Taken together, our results show that the KDM4 demethylases are required for the expression of genes essential for the long-term maintenance of normal hematopoiesis.
机译:KDM4 / JMJD2是H3K9和H3K36特异性去甲基酶,其被认为是治疗患MLL易位的急性髓性白血病(AML)的治疗靶标。 在这里,我们研究了耗尽KDM4活性对正常血液缺陷的长期影响,以探讨了这些酶的连续抑制的潜在副作用。 利用条件KDM4A / KDM4B / KDM4C三敲除小鼠,我们表明造血干细胞(HSC)维护需要KDM4活性。 KDM4去甲基酶的敲除导致H3K9ME3对转录起始位点的积累和HSC中几种基因表达的相应下调。 我们表明,这些基因中的2个TAF1B和NOM1对于维持造血细胞至关重要。 我们的结果表明,KDM4去甲基化酶是表达对于正常血液缺血的长期维持至关重要的基因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号