Suppr超能文献

primiref:一种用于分析单细胞测序数据中初级-miRNA 表达的参考。

primiReference: a reference for analysis of primary-microRNA expression in single-nucleus sequencing data.

机构信息

Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, 02903, USA.

Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, 02903, USA.

出版信息

J Genet Genomics. 2023 Feb;50(2):108-121. doi: 10.1016/j.jgg.2022.10.003. Epub 2022 Nov 9.

Abstract

Single-nucleus RNA-sequencing technology has revolutionized understanding of nuanced changes in gene expression between cell types within tissues. Unfortunately, our understanding of regulatory RNAs, such as microRNAs (miRNAs), is limited through both single-cell and single-nucleus techniques due to the short length of miRNAs in the cytoplasm and the incomplete reference of longer primary miRNA (pri-miRNA) transcripts in the nucleus. We build a custom reference to align and count pri-miRNA sequences in single-nucleus data. Using young and aged subventricular zone (SVZ) nuclei, we show differential expression of pri-miRNAs targeting genes involved in neural stem cells (NSC) differentiation in the aged SVZ. Furthermore, using wild-type and 5XFAD mouse model cortex nuclei, to validate the use of primiReference, we find cell-type-specific expression of pri-miRNAs known to be involved in Alzheimer's disease (AD). pri-miRNAs likely contribute to NSC dysregulation with age and AD pathology. primiReference is paramount in capturing a global profile of gene expression and regulation in single-nucleus data and can provide key insights into cell-type-specific expression of pri-miRNAs, paving the way for future studies of regulation and pathway dysregulation. By looking at pri-miRNA abundance and transcriptional differences, regulation of gene expression by miRNAs in disease and aging can be further explored.

摘要

单细胞 RNA 测序技术极大地推动了我们对组织内细胞类型间基因表达细微变化的理解。不幸的是,由于细胞质中 miRNA 长度较短,以及细胞核中较长的初级 miRNA (pri-miRNA) 转录本参考不完整,单细胞和单核技术限制了我们对调控 RNA(如 microRNA (miRNA))的理解。我们构建了一个自定义的参考,以对齐和计数单核数据中的 pri-miRNA 序列。使用年轻和衰老的侧脑室下区 (SVZ) 核,我们展示了靶向参与衰老 SVZ 神经干细胞 (NSC) 分化的基因的 pri-miRNAs 的差异表达。此外,使用野生型和 5XFAD 小鼠模型皮质核,验证了 primiReference 的使用,我们发现已知与阿尔茨海默病 (AD) 相关的 pri-miRNAs 在细胞类型特异性表达。pri-miRNAs 可能与年龄相关的 NSC 失调和 AD 病理有关。primireference 对于捕获单核数据中基因表达和调控的全局特征至关重要,并为 pri-miRNA 的细胞类型特异性表达提供了关键见解,为未来的调控和通路失调研究铺平了道路。通过观察 pri-miRNA 的丰度和转录差异,可以进一步研究 miRNA 在疾病和衰老中对基因表达的调控。

相似文献

1
primiReference: a reference for analysis of primary-microRNA expression in single-nucleus sequencing data.
J Genet Genomics. 2023 Feb;50(2):108-121. doi: 10.1016/j.jgg.2022.10.003. Epub 2022 Nov 9.
3
PPMS: A framework to Profile Primary MicroRNAs from Single-cell RNA-sequencing datasets.
Brief Bioinform. 2022 Nov 19;23(6). doi: 10.1093/bib/bbac419.
4
High-Throughput Characterization of Primary microRNA Transcripts.
Methods Mol Biol. 2018;1823:1-9. doi: 10.1007/978-1-4939-8624-8_1.
5
Genetic control of primary microRNA insight into cis- and trans-regulatory variations by RNA-seq.
Gene. 2013 Apr 1;517(2):224-9. doi: 10.1016/j.gene.2012.08.015. Epub 2013 Jan 3.
6
Human microRNAs are processed from capped, polyadenylated transcripts that can also function as mRNAs.
RNA. 2004 Dec;10(12):1957-66. doi: 10.1261/rna.7135204. Epub 2004 Nov 3.
7
Transcriptional, post-transcriptional and chromatin-associated regulation of pri-miRNAs, pre-miRNAs and moRNAs.
Nucleic Acids Res. 2016 Apr 20;44(7):3070-81. doi: 10.1093/nar/gkv1354. Epub 2015 Dec 15.
8
STV1, a ribosomal protein, binds primary microRNA transcripts to promote their interaction with the processing complex in Arabidopsis.
Proc Natl Acad Sci U S A. 2017 Feb 7;114(6):1424-1429. doi: 10.1073/pnas.1613069114. Epub 2017 Jan 23.
9
Microprocessor dynamics shows co- and post-transcriptional processing of pri-miRNAs.
RNA. 2017 Jun;23(6):892-898. doi: 10.1261/rna.060715.117. Epub 2017 Mar 1.
10
Frequency and fate of microRNA editing in human brain.
Nucleic Acids Res. 2008 Sep;36(16):5270-80. doi: 10.1093/nar/gkn479. Epub 2008 Aug 6.

本文引用的文献

1
MicroRNA-582-5p Contributes to the Maintenance of Neural Stem Cells Through Inhibiting Secretory Protein FAM19A1.
Front Cell Neurosci. 2022 May 24;16:866020. doi: 10.3389/fncel.2022.866020. eCollection 2022.
2
CircRNA-ceRNA Network Revealing the Potential Regulatory Roles of CircRNA in Alzheimer's Disease Involved the cGMP-PKG Signal Pathway.
Front Mol Neurosci. 2021 May 21;14:665788. doi: 10.3389/fnmol.2021.665788. eCollection 2021.
4
Loss of miR-23b/27b/24-1 Cluster Impairs Glucose Tolerance via Glycolysis Pathway in Mice.
Int J Mol Sci. 2021 Jan 7;22(2):550. doi: 10.3390/ijms22020550.
5
Single-Nucleus RNA-Seq Is Not Suitable for Detection of Microglial Activation Genes in Humans.
Cell Rep. 2020 Sep 29;32(13):108189. doi: 10.1016/j.celrep.2020.108189.
7
Sialylation and Galectin-3 in Microglia-Mediated Neuroinflammation and Neurodegeneration.
Front Cell Neurosci. 2020 Jun 9;14:162. doi: 10.3389/fncel.2020.00162. eCollection 2020.
8
Systematic comparison of single-cell and single-nucleus RNA-sequencing methods.
Nat Biotechnol. 2020 Jun;38(6):737-746. doi: 10.1038/s41587-020-0465-8. Epub 2020 Apr 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验