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RNA干扰机制的亚细胞拓扑结构是多方面的,并揭示了黏着连接是上皮细胞的枢纽。

The subcellular topology of the RNAi machinery is multifaceted and reveals adherens junctions as an epithelial hub.

作者信息

Nair-Menon Joyce, Kingsley Christina, Mesnaoui Houda, Risner Alyssa, Jarvis Jordan E, Lin Peter, Wilson Kyrie, Rohrer Bärbel, Kourtidis Antonis

机构信息

Department of Regenerative Medicine and Cell Biology, Medical University South Carolina, Charleston, SC, USA.

Department of Ophthalmology, Medical University South Carolina, Charleston, SC, USA.

出版信息

Sci Rep. 2025 Jul 10;15(1):24814. doi: 10.1038/s41598-025-09795-1.

DOI:10.1038/s41598-025-09795-1
PMID:40640449
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12246189/
Abstract

The RNA interference (RNAi) machinery is a key cellular mechanism catalyzing biogenesis and function of miRNAs to post-transcriptionally regulate mRNA expression. The RNAi machinery includes a set of protein complexes with subcellular localization traditionally presented in a uniform fashion: the microprocessor processes miRNAs in the nucleus, whereas the DICER and the RNA-induced silencing complex (RISC) further process and enable activity of miRNAs in the cytoplasm. However, several studies have identified subcellular patterns of RNAi components that deviate from this model. We have particularly shown that RNAi complexes associate with the adherens junctions of well-differentiated epithelial cells, through the E-cadherin partner PLEKHA7. To assess the extent of these subcellular topological patterns, we examined subcellular localization of the microprocessor and RISC in a series of human cell lines and normal human tissues. Our results show that junctional localization of RNAi components is a broad characteristic of differentiated epithelia, but it is absent in transformed or mesenchymal cells and tissues. We also find extensive localization of the microprocessor in the cytoplasm, as well as of RISC in the nucleus. These findings expose a RNAi machinery with multifaceted subcellular topology that may inform its physiological role and calls for updating of the current models.

摘要

RNA干扰(RNAi)机制是一种关键的细胞机制,可催化微小RNA(miRNA)的生物合成和功能,从而在转录后调节信使核糖核酸(mRNA)的表达。RNAi机制包括一组蛋白质复合物,其亚细胞定位传统上以统一的方式呈现:微处理器在细胞核中加工miRNA,而Dicer酶和RNA诱导沉默复合体(RISC)则在细胞质中进一步加工并使miRNA发挥活性。然而,多项研究已经确定了RNAi组分的亚细胞分布模式与该模型不符。我们特别表明,RNAi复合物通过E-钙黏蛋白的伴侣PLEKHA7与分化良好的上皮细胞的黏着连接相关联。为了评估这些亚细胞拓扑模式的程度,我们检测了一系列人类细胞系和正常人体组织中微处理器和RISC的亚细胞定位。我们的结果表明,RNAi组分的连接定位是分化上皮细胞的一个广泛特征,但在转化细胞或间充质细胞及组织中不存在。我们还发现微处理器在细胞质中广泛定位,以及RISC在细胞核中广泛定位。这些发现揭示了一种具有多方面亚细胞拓扑结构的RNAi机制,这可能为其生理作用提供线索,并要求更新当前的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/2f38735f59a9/41598_2025_9795_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/96ae0efe5613/41598_2025_9795_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/ed0e131bf1c8/41598_2025_9795_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/f7bd96776315/41598_2025_9795_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/00719754b6f7/41598_2025_9795_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/917d6a2a7b48/41598_2025_9795_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/4cd6587c6941/41598_2025_9795_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/6558d9ee9e6b/41598_2025_9795_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/2f38735f59a9/41598_2025_9795_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/96ae0efe5613/41598_2025_9795_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/ed0e131bf1c8/41598_2025_9795_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/f7bd96776315/41598_2025_9795_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/00719754b6f7/41598_2025_9795_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/917d6a2a7b48/41598_2025_9795_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/4cd6587c6941/41598_2025_9795_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/6558d9ee9e6b/41598_2025_9795_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1883/12246189/2f38735f59a9/41598_2025_9795_Fig8_HTML.jpg

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