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Myofibril-Inducing RNA (MIR) is essential for tropomyosin expression and myofibrillogenesis in axolotl hearts

机译:肌原纤维诱导RNA(MIR)对于原核心脏中原肌球蛋白的表达和肌原纤维形成至关重要

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摘要

The Mexican axolotl, Ambystoma mexicanum, carries the naturally-occurring recessive mutant gene 'c' that results in a failure of homozygous (c/c) embryos to form hearts that beat because of an absence of organized myofibrils. Our previous studies have shown that a noncoding RNA, Myofibril-Inducing RNA (MIR), is capable of promoting myofibrillogenesis and heart beating in the mutant (c/c) axolotls. The present study demonstrates that the MIR gene is essential for tropomyosin (TM) expression in axolotl hearts during development. Gene expression studies show that mRNA expression of various tropomyosin isoforms in untreated mutant hearts and in normal hearts knocked down with double-stranded MIR (dsMIR) are similar to untreated normal. However, at the protein level, selected tropomyosin isoforms are significantly reduced in mutant and dsMIR treated normal hearts. These results suggest that MIR is involved in controlling the translation or post-translation of various TM isoforms and subsequently of regulating cardiac contractility.
机译:墨西哥a,Ambystoma mexicanum携带天然存在的隐性突变基因“ c”,该基因导致纯合(c / c)胚胎无法形成由于缺乏有组织的肌原纤维而跳动的心脏。我们以前的研究表明,非编码RNA,肌原纤维诱导RNA(MIR),能够促进突变(c / c)轴突中的肌原纤维形成和心脏跳动。本研究表明,在发育过程中,MIR基因对于原核心脏中原肌球蛋白(TM)的表达至关重要。基因表达研究表明,在未经治疗的突变心脏和被双链MIR(dsMIR)击倒的正常心脏中,各种原肌球蛋白同工型的mRNA表达与未经治疗的正常人相似。但是,在蛋白质水平上,在突变和dsMIR治疗的正常心脏中,选择的原肌球蛋白同工型显着降低。这些结果表明,MIR参与控制各种TM同工型的翻译或翻译后,并随后调节心脏的收缩力。

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