PAX6和NFAT4作为神经元祖细胞长链非编码RNA Mrhl转录调控因子的鉴定

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2022-11-17 DOI:10.1128/mcb.00036-22
Debosree Pal, Sangeeta Dutta, Dhanur P Iyer, Deepika Shriram, Utsa Bhaduri, M R S Rao
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引用次数: 1

摘要

长链非编码RNA (lncRNA) Mrhl已被证明参与协调小鼠精原祖细胞的减数分裂和小鼠胚胎干细胞的分化事件。在这里,我们描述了Mrhl与谱系特异性转录因子在小鼠神经元谱系发育过程中的相互作用。我们的研究结果表明,Mrhl在小鼠胚胎脑的神经祖细胞群和维甲酸衍生的放射状胶质样神经祖细胞中表达。Mrhl的缺失导致神经元祖细胞早期分化到更稳定的状态。主转录因子PAX6直接与Mrhl启动子的远端启动子的主要位点结合,位于Mrhl转录起始位点(TSS)上游2.9 kb处。此外,NFAT4在两个位点占据mrhl -近端启动子,分别位于TSS上游437个碱基对(bp)和143个bp。PAX6和NFAT4的独立敲除研究证实它们调节神经元祖细胞中Mrhl的表达。我们还发现PAX6和NFAT4在相同的染色质复合体中相互结合。在pax6结合的染色质中,NFAT4占据Mrhl启动子,暗示Mrhl可能协同调控。我们的研究对于理解lncrna如何受到主要谱系特异性转录因子的调控,从而定义特定的发育和分化事件至关重要。
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Identification of PAX6 and NFAT4 as the Transcriptional Regulators of the Long Noncoding RNA Mrhl in Neuronal Progenitors.

The long noncoding RNA (lncRNA) Mrhl has been shown to be involved in coordinating meiotic commitment of mouse spermatogonial progenitors and differentiation events in mouse embryonic stem cells. Here, we characterized the interplay of Mrhl with lineage-specific transcription factors during mouse neuronal lineage development. Our results demonstrate that Mrhl is expressed in the neuronal progenitor populations in mouse embryonic brains and in retinoic acid-derived radial-glia-like neuronal progenitor cells. Depletion of Mrhl leads to early differentiation of neuronal progenitors to a more committed state. A master transcription factor, PAX6, directly binds to the Mrhl promoter at a major site in the distal promoter, located at 2.9 kb upstream of the transcription start site (TSS) of Mrhl. Furthermore, NFAT4 occupies the Mrhl-proximal promoter at two sites, at 437 base pairs (bp) and 143 bp upstream of the TSS. Independent knockdown studies for PAX6 and NFAT4 confirm that they regulate Mrhl expression in neuronal progenitors. We also show that PAX6 and NFAT4 associate with each other in the same chromatin complex. NFAT4 occupies the Mrhl promoter in PAX6-bound chromatin, implying possible coregulation of Mrhl. Our studies are crucial for understanding how lncRNAs are regulated by major lineage-specific transcription factors, in order to define specific development and differentiation events.

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7.20
自引率
4.30%
发文量
567
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