Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
The RNA interference (RNAi) machinery is an essential component of the cell, regulating miRNA biogenesis and function. RNAi complexes were thought to localize either in the nucleus, such as the microprocessor, or in the cytoplasm, such as the RNA-induced silencing complex (RISC). We recently reveale...
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creator | Nair-Menon, Joyce Daulagala, Amanda C Connor, Dean M Rutledge, Lauren Penix, Trevor Bridges, Mary Catherine Wellslager, Bridgette Spyropoulos, Demetri D Timmers, Cynthia D Broome, Ann-Marie Kourtidis, Antonis |
description | The RNA interference (RNAi) machinery is an essential component of the cell, regulating miRNA biogenesis and function. RNAi complexes were thought to localize either in the nucleus, such as the microprocessor, or in the cytoplasm, such as the RNA-induced silencing complex (RISC). We recently revealed that the core microprocessor components DROSHA and DGCR8, as well as the main components of RISC, including Ago2, also associate with the apical adherens junctions of well-differentiated cultured epithelial cells. Here, we demonstrate that the localization of the core RNAi components is specific and predominant at apical areas of cell-cell contact of human normal colon epithelial tissues and normal primary colon epithelial cells. Importantly, the apical junctional localization of RNAi proteins is disrupted or lost in human colon tumors and in poorly differentiated colon cancer cell lines, correlating with the dysregulation of the adherens junction component PLEKHA7. We show that the restoration of PLEKHA7 expression at adherens junctions of aggressively tumorigenic colon cancer cells restores the junctional localization of RNAi components and suppresses cancer cell growth in vitro and in vivo. In summary, this work identifies the apical junctional localization of the RNAi machinery as a key feature of the differentiated colonic epithelium, with a putative tumor suppressing function. |
doi_str_mv | 10.3390/ijms21072559 |
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RNAi complexes were thought to localize either in the nucleus, such as the microprocessor, or in the cytoplasm, such as the RNA-induced silencing complex (RISC). We recently revealed that the core microprocessor components DROSHA and DGCR8, as well as the main components of RISC, including Ago2, also associate with the apical adherens junctions of well-differentiated cultured epithelial cells. Here, we demonstrate that the localization of the core RNAi components is specific and predominant at apical areas of cell-cell contact of human normal colon epithelial tissues and normal primary colon epithelial cells. Importantly, the apical junctional localization of RNAi proteins is disrupted or lost in human colon tumors and in poorly differentiated colon cancer cell lines, correlating with the dysregulation of the adherens junction component PLEKHA7. We show that the restoration of PLEKHA7 expression at adherens junctions of aggressively tumorigenic colon cancer cells restores the junctional localization of RNAi components and suppresses cancer cell growth in vitro and in vivo. In summary, this work identifies the apical junctional localization of the RNAi machinery as a key feature of the differentiated colonic epithelium, with a putative tumor suppressing function.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21072559</identifier><identifier>PMID: 32272708</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adherens junctions ; Adherens Junctions - metabolism ; Agreements ; Animals ; Argonaute 2 protein ; Carcinogenesis - metabolism ; Cell adhesion ; Cell adhesion & migration ; Cell differentiation ; Cell Line ; Cell Proliferation - physiology ; Colon ; Colon - metabolism ; Colon cancer ; Colonic Neoplasms - metabolism ; Colorectal cancer ; Cytoplasm ; Cytoplasm - metabolism ; Epithelial cells ; Epithelial Cells - metabolism ; Epithelium ; Female ; Gene expression ; Humans ; Intestinal Mucosa - metabolism ; Localization ; Male ; Mice ; Microprocessors ; MicroRNAs - metabolism ; Microscopy ; miRNA ; Ribonuclease III - metabolism ; RNA Interference - physiology ; RNA-Binding Proteins - metabolism ; RNA-induced silencing complex ; RNA-mediated interference ; Tumor cell lines ; Tumorigenesis ; Tumors</subject><ispartof>International journal of molecular sciences, 2020-04, Vol.21 (7), p.2559</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). 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We show that the restoration of PLEKHA7 expression at adherens junctions of aggressively tumorigenic colon cancer cells restores the junctional localization of RNAi components and suppresses cancer cell growth in vitro and in vivo. 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subjects | Adherens junctions Adherens Junctions - metabolism Agreements Animals Argonaute 2 protein Carcinogenesis - metabolism Cell adhesion Cell adhesion & migration Cell differentiation Cell Line Cell Proliferation - physiology Colon Colon - metabolism Colon cancer Colonic Neoplasms - metabolism Colorectal cancer Cytoplasm Cytoplasm - metabolism Epithelial cells Epithelial Cells - metabolism Epithelium Female Gene expression Humans Intestinal Mucosa - metabolism Localization Male Mice Microprocessors MicroRNAs - metabolism Microscopy miRNA Ribonuclease III - metabolism RNA Interference - physiology RNA-Binding Proteins - metabolism RNA-induced silencing complex RNA-mediated interference Tumor cell lines Tumorigenesis Tumors |
title | Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer |
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