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miR-191 regulates mouse erythroblast enucleation by down-regulating Riok3 and Mxi1.

机译:miR-191通过下调Riok3和Mxi1来调节小鼠成红细胞的去核。

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Using RNA-seq technology, we found that the majority of microRNAs (miRNAs) present in CFU-E erythroid progenitors are down-regulated during terminal erythroid differentiation. Of the developmentally down-regulated miRNAs, ectopic overexpression of miR-191 blocks erythroid enucleation but has minor effects on proliferation and differentiation. We identified two erythroid-enriched and developmentally up-regulated genes, Riok3 and Mxi1, as direct targets of miR-191. Knockdown of either Riok3 or Mxi1 blocks enucleation, and either physiological overexpression of miR-191 or knockdown of Riok3 or Mxi1 blocks chromatin condensation. Thus, down-regulation of miR-191 is essential for erythroid chromatin condensation and enucleation by allowing up-regulation of Riok3 and Mxi1.
机译:使用RNA-seq技术,我们发现存在于CFU-E红系祖细胞中的大多数microRNA(miRNA)在红系终末分化过程中被下调。在发育中下调的miRNA中,miR-191的异位过表达会阻止类红细胞摘除,但对增殖和分化影响较小。我们确定了两个富含类红素且发育上调的基因Riok3和Mxi1作为miR-191的直接靶标。敲除Riok3或Mxi1会阻断去核,而生理上过量表达miR-191或敲除Riok3或Mxi1会阻止染色质浓缩。因此,通过允许Riok3和Mxi1的上调,miR-191的下调对于红细胞染色质的浓缩和去核至关重要。

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