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Multimodal Long Noncoding RNA Interaction Networks: Control Panels for Cell Fate Specification

机译:多模式长度非划分RNA相互作用网络:用于细胞命运规范的控制面板

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摘要

Lineage specification in early development is the basis for the exquisitely precise body plan of multicellular organisms. It is therefore critical to understand cell fate decisions in early development. Moreover, for regenerative medicine, the accurate specification of cell types to replace damaged/diseased tissue is strongly dependent on identifying determinants of cell identity. Long noncoding RNAs (lncRNAs) have been shown to regulate cellular plasticity, including pluripotency establishment and maintenance, differentiation and development, yet broad phenotypic analysis and the mechanistic basis of their function remains lacking. As components of molecular condensates, lncRNAs interact with almost all classes of cellular biomolecules, including proteins, DNA, mRNAs, and microRNAs. With functions ranging from controlling alternative splicing of mRNAs, to providing scaffolding upon which chromatin modifiers are assembled, it is clear that at least a subset of lncRNAs are far from the transcriptional noise they were once deemed. This review highlights the diversity of lncRNA interactions in the context of cell fate specification, and provides examples of each type of interaction in relevant developmental contexts. Also highlighted are experimental and computational approaches to study lncRNAs.
机译:早期发展中的谱系规范是多细胞生物体精确的体内计划的基础。因此,了解早期发展中的细胞命运决策至关重要。此外,对于再生药物,用于替换受损/患病组织的细胞类型的准确规范是强烈的依赖性​​鉴定细胞标识的确定性。已经证明了长的非编码RNA(LNCRNA)调节细胞可塑性,包括多能性建立和维护,分化和开发,但其功能的机械型依据仍然缺乏。作为分子缩合物的组分,LNCRNA与几乎所有类别的细胞生物分子相互作用,包括蛋白质,DNA,MRNA和MicroRNA。利用函数来控制MRNA的替代剪接,为了提供组装染色质调节剂的脚手架,显然,至少一种LNCRNA的子集远远远非它们一次被认为的转录噪声。该综述突出了细胞命运规范的背景下LNCRNA相互作用的多样性,并提供了相关发展环境中每种类型的相互作用的例子。还强调了研究LNCRNA的实验和计算方法。

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