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Opposing Roles for the lncRNA Haunt and Its Genomic Locus in Regulating HOXA Gene Activation during Embryonic Stem Cell Differentiation

机译:lncRNA困扰及其基因组座位在胚胎干细胞分化过程中调节HOXA基因激活中的相反作用。

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Long noncoding RNAs (lncRNAs) have been implicated in controlling various aspects of embryonic stem cell (ESC) biology, although the functions of specific lncRNAs, and the molecular mechanisms through which they act, remain unclear. Here, we demonstrate discrete and opposing roles for the lncRNA transcript Haunt and its genomic locus in regulating the HOXA gene cluster during ESC differentiation. Reducing or enhancing Haunt expression, with minimal disruption of the Haunt locus, led to upregulation or downregulation of HOXA genes, respectively. In contrast, increasingly large genomic deletions within the Haunt locus attenuated HOXA activation. The Haunt DNA locus contains potential enhancers of HOXA activation, whereas Haunt RNA acts to prevent aberrant HOXA expression. This work reveals a multifaceted model of lncRNA-mediated transcriptional regulation of the HOXA cluster, with distinct roles for a lncRNA transcript and its genomic locus, while illustrating the power of rapid CRISPR/Cas9-based genome editing for assigning lncRNA functions.
机译:长的非编码RNA(lncRNA)已牵涉控制胚胎干细胞(ESC)生物学的各个方面,尽管具体lncRNA的功能以及它们通过其发挥作用的分子机制尚不清楚。在这里,我们展示了lncRNA转录产物Haunt及其基因座在ESC分化过程中调控HOXA基因簇中的离散和相对作用。减少或增强Haunt表达,同时最小化Haunt基因座的破坏,分别导致HOXA基因的上调或下调。相反,Haunt位点内越来越大的基因组缺失减弱了HOXA激活。 Haunt DNA基因座含有潜在的HOXA激活增强剂,而Haunt RNA则可防止HOXA异常表达。这项工作揭示了lncRNA介导的HOXA簇转录调控的多方面模型,对lncRNA转录本及其基因组位点具有独特的作用,同时说明了基于CRISPR / Cas9的快速基因组编辑对分配lncRNA功能的作用。

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