Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, TX 76019, USA.
FEBS J. 2010 Apr;277(8):1790-804. doi: 10.1111/j.1742-4658.2010.07606.x. Epub 2010 Mar 4.
Mixed lineage leukemias (MLLs) are an evolutionarily conserved trithorax family of human genes that play critical roles in HOX gene regulation and embryonic development. MLL1 is well known to be rearranged in myeloid and lymphoid leukemias in children and adults. There are several MLL family proteins such as MLL1, MLL2, MLL3, MLL4, MLL5, Set1A and Set1B, and each possesses histone H3 lysine 4 (H3K4)-specific methyltransferase activity and has critical roles in gene activation and epigenetics. Although MLLs are recognized as major regulators of gene activation, their mechanism of action, target genes and the distinct functions of different MLLs remain elusive. Recent studies demonstrate that besides H3K4 methylation and HOX gene regulation, MLLs have much wider roles in gene activation and regulate diverse other genes. Interestingly, several MLLs interact with nuclear receptors and have critical roles in steroid-hormone-mediated gene activation and signaling. In this minireview, we summarize recent advances in understanding the roles of MLLs in gene regulation and hormone signaling and highlight their potential roles in mRNA processing.
混合谱系白血病(MLLs)是一个进化上保守的人类三结构域基因家族,在 HOX 基因调控和胚胎发育中发挥着关键作用。MLL1 在儿童和成人的髓系和淋巴白血病中被证实存在重排。有几种 MLL 家族蛋白,如 MLL1、MLL2、MLL3、MLL4、MLL5、Set1A 和 Set1B,它们都具有组蛋白 H3 赖氨酸 4(H3K4)特异性甲基转移酶活性,在基因激活和表观遗传学中发挥着关键作用。尽管 MLLs 被认为是基因激活的主要调节因子,但它们的作用机制、靶基因以及不同 MLLs 的独特功能仍不清楚。最近的研究表明,除了 H3K4 甲基化和 HOX 基因调控外,MLLs 在基因激活和调节多种其他基因方面具有更广泛的作用。有趣的是,有几个 MLLs 与核受体相互作用,在甾体激素介导的基因激活和信号转导中发挥着关键作用。在这篇综述中,我们总结了 MLLs 在基因调控和激素信号转导中的作用的最新进展,并强调了它们在 mRNA 处理中的潜在作用。