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Eukaryotic gene expression: understanding the role of UPF1 in global mRNA processing and amyotrophic lateral sclerosis (ALS)

Eukaryotic gene expression: understanding the role of UPF1 in global mRNA processing and amyotrophic lateral sclerosis (ALS)
真核基因表达:了解 UPF1 在整体 mRNA 加工和肌萎缩侧索硬化症 (ALS) 中的作用
批准号:
2264958
负责人:
金额:
$0.0万
依托单位:
依托单位国家:
英国
项目类别:
Studentship
财政年份:
2019
资助国家:
英国
项目状态:
已结题
起止时间:
2019 至 --

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中文摘要
翻译
UPF1是一种RNA解旋酶,因其在调节无义介导的mRNA衰变(NMD)中的细胞质作用而被广泛讨论。NMD是一种能够检测和降解异常mrna的质量控制机制。由于NMD涉及mRNA调控的许多步骤,因此它对药物靶向特别感兴趣。引人注目的是,UPF1是肌萎缩性侧索硬化症(ALS)的候选药物,因为有证据表明,在ALS大鼠模型中,人类UPF1的表达可以恢复运动功能(Jackson et al., 2015)。然而,UPF1的功能作用仍不明确。最近的证据表明,UPF1在果蝇的细胞核中起作用,在那里它与活性基因相关,允许适当的mRNA包装和输出(Singh等人,2019)。尽管如此,UPF1对新生mrna的招募及其核作用仍然知之甚少。这些作用对于揭示UPF1如何作为神经退行性疾病的药物靶点至关重要。该项目结合干湿实验室程序来解决UPF1在全球mRNA加工中的作用。有证据表明,在UPF1耗尽的条件下,核聚集体形成,这意味着这种蛋白质是转录组稳态所必需的(Singh等人,2019)。因此,包括RNA-seq, ChIP-seq和SLAM-seq在内的技术将显示UPF1如何相互作用并影响前mrna,探索其与新生转录物的关联及其在其适当剪接,包装和输出中的作用。
英文摘要
UPF1 is an RNA helicase commonly discussed for its cytoplasmic roles in modulating nonsense-mediated mRNA decay (NMD). NMD is a quality control mechanism which enables the detection and degradation of aberrant mRNAs. NMD is of particular interest for drug targeting, as it involves many steps of mRNA regulation. Strikingly, UPF1 is a candidate drug for amyotrophic lateral sclerosis (ALS) as there is evidence that expression of human UPF1 restores motor function in a rat model of ALS (Jackson et al., 2015). However, the functional roles of UPF1 remain inconclusive. Recent evidence shows that UPF1 functions in the nuclei of Drosophila, where it associates with active genes allowing for appropriate mRNA packaging and export (Singh et al., 2019). Despite this, UPF1 recruitment to nascent mRNAs and its nuclear roles remain poorly understood. Such roles are crucial to uncover for the appropriate understanding of how UPF1 can be used as a drug target in neurodegenerative diseases. This project combines wet and dry-lab procedures to address the roles of UPF1 on global mRNA processing. Evidence shows that in UPF1 depleted conditions, nuclear aggregates form, meaning this protein is required for transcriptome homeostasis (Singh et al., 2019). Thus, techniques including RNA-seq, ChIP-seq and SLAM-seq will show how UPF1 interacts and affects pre-mRNAs exploring its association with nascent transcripts and its roles in their appropriate splicing, packaging and export.
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