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Qki5 通过前体 mRNA 处理来定义运动神经元特异性转录组,从而保障脊髓运动神经元功能。

Qki5 safeguards spinal motor neuron function by defining the motor neuron-specific transcriptome via pre-mRNA processing.

机构信息

Division of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Chuo-ku, Niigata 951-8510, Japan.

Keio University Regenerative Medicine Research Center, Kawasaki, Kanagawa 210-0821, Japan.

出版信息

Proc Natl Acad Sci U S A. 2024 Sep 10;121(37):e2401531121. doi: 10.1073/pnas.2401531121. Epub 2024 Sep 3.

DOI:10.1073/pnas.2401531121
PMID:39226364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11406248/
Abstract

Many RNA-binding proteins (RBPs) are linked to the dysregulation of RNA metabolism in motor neuron diseases (MNDs). However, the molecular mechanisms underlying MN vulnerability have yet to be elucidated. Here, we found that such an RBP, Quaking5 (Qki5), contributes to formation of the MN-specific transcriptome profile, termed "MN-ness," through the posttranscriptional network and maintenance of the mature MNs. Immunohistochemical analysis and single-cell RNA sequencing (scRNA-seq) revealed that Qki5 is predominantly expressed in MNs, but not in other neuronal populations of the spinal cord. Furthermore, comprehensive RNA sequencing (RNA-seq) analyses revealed that Qki5-dependent RNA regulation plays a pivotal role in generating the MN-specific transcriptome through pre-messenger ribonucleic acid (mRNA) splicing for the synapse-related molecules and c-Jun N-terminal kinase/stress-activated protein kinase (JNK/SAPK) signaling pathways. Indeed, MN-specific ablation of the Qki5 caused neurodegeneration in postnatal mice and loss of Qki5 function resulted in the aberrant activation of stress-responsive JNK/SAPK pathway both in vitro and in vivo. These data suggested that Qki5 plays a crucial biological role in RNA regulation and safeguarding of MNs and might be associated with pathogenesis of MNDs.

摘要

许多 RNA 结合蛋白(RBPs)与运动神经元疾病(MNDs)中 RNA 代谢的失调有关。然而,MN 易损性的分子机制尚未阐明。在这里,我们发现一种名为 Quaking5(Qki5)的 RBP 通过转录后网络和成熟 MN 的维持,有助于形成 MN 特异性转录组谱,称为“MN 特征”。免疫组织化学分析和单细胞 RNA 测序(scRNA-seq)显示,Qki5 在 MN 中表达,而在脊髓中的其他神经元群体中不表达。此外,全面的 RNA 测序(RNA-seq)分析表明,Qki5 依赖性 RNA 调节通过与突触相关分子和 c-Jun N 端激酶/应激激活蛋白激酶(JNK/SAPK)信号通路相关的前信使 RNA(mRNA)剪接,在产生 MN 特异性转录组中起着关键作用。事实上,Qki5 在 MN 中的特异性缺失导致出生后小鼠的神经退行性变,并且 Qki5 功能的丧失导致应激反应性 JNK/SAPK 通路在体外和体内的异常激活。这些数据表明,Qki5 在 RNA 调节和 MN 的保护中发挥着至关重要的生物学作用,并且可能与 MND 的发病机制有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/2dfea587c040/pnas.2401531121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/e8889507d332/pnas.2401531121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/4413f4bfa60f/pnas.2401531121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/a68b25096ca5/pnas.2401531121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/c761ef55265d/pnas.2401531121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/2dfea587c040/pnas.2401531121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/e8889507d332/pnas.2401531121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/4413f4bfa60f/pnas.2401531121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/a68b25096ca5/pnas.2401531121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/c761ef55265d/pnas.2401531121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adc/11406248/2dfea587c040/pnas.2401531121fig05.jpg

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