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ALG-1 通过调节剪接因子活性影响肠道和体肌组织中准确的 mRNA 剪接模式。

ALG-1 Influences Accurate mRNA Splicing Patterns in the Intestine and Body Muscle Tissues by Modulating Splicing Factor Activities.

机构信息

Molecular and Cellular Biology Graduate Program, School of Life Sciences, Arizona State University, Tempe, Arizona 85287.

Virginia G. Piper Center for Personalized Diagnostics, The Biodesign Institute at Arizona State University, Tempe, Arizona.

出版信息

Genetics. 2019 Jul;212(3):931-951. doi: 10.1534/genetics.119.302223. Epub 2019 May 9.

Abstract

MicroRNAs (miRNAs) are known to modulate gene expression, but their activity at the tissue-specific level remains largely uncharacterized. To study their contribution to tissue-specific gene expression, we developed novel tools to profile putative miRNA targets in the intestine and body muscle. We validated many previously described interactions and identified ∼3500 novel targets. Many of the candidate miRNA targets curated are known to modulate the functions of their respective tissues. Within our data sets we observed a disparity in the use of miRNA-based gene regulation between the intestine and body muscle. The intestine contained significantly more putative miRNA targets than the body muscle highlighting its transcriptional complexity. We detected an unexpected enrichment of RNA-binding proteins targeted by miRNA in both tissues, with a notable abundance of RNA splicing factors. We developed genetic tools to validate and further study three RNA splicing factors identified as putative miRNA targets in our study (, , and ), and show that these factors indeed contain functional miRNA regulatory elements in their 3'UTRs that are able to repress their expression in the intestine. In addition, the alternative splicing pattern of their respective downstream targets (, , , and ) is dysregulated when the miRNA pathway is disrupted. A reannotation of the transcriptome data in strains that are deficient in the miRNA pathway from past studies supports and expands on our results. This study highlights an unexpected role for miRNAs in modulating tissue-specific gene isoforms, where post-transcriptional regulation of RNA splicing factors associates with tissue-specific alternative splicing.

摘要

微小 RNA(miRNA)被认为可以调节基因表达,但它们在组织特异性水平上的活性在很大程度上仍未被描述。为了研究它们对组织特异性基因表达的贡献,我们开发了新的工具来分析肠道和体肌中的推定 miRNA 靶标。我们验证了许多以前描述的相互作用,并鉴定了约 3500 个新的靶标。许多经过精心筛选的候选 miRNA 靶标被认为可以调节其各自组织的功能。在我们的数据集中,我们观察到 miRNA 对肠道和体肌基因调控的使用存在差异。肠道中的推定 miRNA 靶标明显多于体肌,突出了其转录复杂性。我们在这两种组织中都检测到 miRNA 靶标 RNA 结合蛋白的意外富集,其中 RNA 剪接因子的丰度尤为显著。我们开发了遗传工具来验证和进一步研究我们研究中鉴定为推定 miRNA 靶标的三个 RNA 剪接因子(、和),并表明这些因子在其 3'UTR 中确实含有能够在肠道中抑制其表达的功能性 miRNA 调节元件。此外,当 miRNA 途径被破坏时,它们各自下游靶标的可变剪接模式(、、、和)发生失调。过去研究中 miRNA 途径缺失菌株的转录组数据的重新注释支持并扩展了我们的结果。这项研究强调了 miRNA 在调节组织特异性基因异构体方面的意外作用,其中 RNA 剪接因子的转录后调控与组织特异性可变剪接相关。

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RNA Splicing and Disease: Animal Models to Therapies.RNA 剪接与疾病:从动物模型到治疗策略。
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