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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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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177752/
https://www.ncbi.nlm.nih.gov/pubmed/32272708
http://dx.doi.org/10.3390/ijms21072559
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author 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
author_facet 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
author_sort Nair-Menon, Joyce
collection PubMed
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.
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spelling pubmed-71777522020-04-28 Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer 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 Int J Mol Sci Article 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. MDPI 2020-04-07 /pmc/articles/PMC7177752/ /pubmed/32272708 http://dx.doi.org/10.3390/ijms21072559 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
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
Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
title Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
title_full Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
title_fullStr Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
title_full_unstemmed Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
title_short Predominant Distribution of the RNAi Machinery at Apical Adherens Junctions in Colonic Epithelia Is Disrupted in Cancer
title_sort predominant distribution of the rnai machinery at apical adherens junctions in colonic epithelia is disrupted in cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177752/
https://www.ncbi.nlm.nih.gov/pubmed/32272708
http://dx.doi.org/10.3390/ijms21072559
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