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Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves
tRNA-derived fragments have been reported in many different organisms and have diverse cellular roles, such as regulating gene expression, inhibiting protein translation, silencing transposable elements, and modulating cell proliferation. In particular, tRNA halves, a class of tRNA fragments produce...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127584/ https://www.ncbi.nlm.nih.gov/pubmed/36809068 http://dx.doi.org/10.1128/mbio.03450-22 |
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author | Sharma, Manu Zhang, Hanbang Ehrenkaufer, Gretchen Singh, Upinder |
author_facet | Sharma, Manu Zhang, Hanbang Ehrenkaufer, Gretchen Singh, Upinder |
author_sort | Sharma, Manu |
collection | PubMed |
description | tRNA-derived fragments have been reported in many different organisms and have diverse cellular roles, such as regulating gene expression, inhibiting protein translation, silencing transposable elements, and modulating cell proliferation. In particular, tRNA halves, a class of tRNA fragments produced by the cleavage of tRNAs in the anti-codon loop, have been widely reported to accumulate under stress and regulate translation in cells. Here, we report the presence of tRNA-derived fragments in Entamoeba, with tRNA halves being the most abundant. We further established that tRNA halves accumulate in the parasites upon different stress stimuli such as oxidative stress, heat shock, and serum starvation. We also observed differential expression of tRNA halves during developmental changes of trophozoite-to-cyst conversion, with various tRNA halves accumulating during early encystation. In contrast to other systems, the stress response does not appear to be mediated by a few specific tRNA halves, as multiple tRNAs appear to be processed during the various stresses. Furthermore, we identified some tRNA-derived fragments associated with Entamoeba Argonaute proteins, EhAgo2-2 and EhAgo2-3, which have a preference for different tRNA-derived fragment species. Finally, we show that tRNA halves are packaged inside extracellular vesicles secreted by amoebas. The ubiquitous presence of tRNA-derived fragments, their association with the Argonaute proteins, and the accumulation of tRNA halves during multiple different stresses, including encystation, suggest a nuanced level of gene expression regulation mediated by different tRNA-derived fragments in Entamoeba. |
format | Online Article Text |
id | pubmed-10127584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101275842023-04-26 Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves Sharma, Manu Zhang, Hanbang Ehrenkaufer, Gretchen Singh, Upinder mBio Research Article tRNA-derived fragments have been reported in many different organisms and have diverse cellular roles, such as regulating gene expression, inhibiting protein translation, silencing transposable elements, and modulating cell proliferation. In particular, tRNA halves, a class of tRNA fragments produced by the cleavage of tRNAs in the anti-codon loop, have been widely reported to accumulate under stress and regulate translation in cells. Here, we report the presence of tRNA-derived fragments in Entamoeba, with tRNA halves being the most abundant. We further established that tRNA halves accumulate in the parasites upon different stress stimuli such as oxidative stress, heat shock, and serum starvation. We also observed differential expression of tRNA halves during developmental changes of trophozoite-to-cyst conversion, with various tRNA halves accumulating during early encystation. In contrast to other systems, the stress response does not appear to be mediated by a few specific tRNA halves, as multiple tRNAs appear to be processed during the various stresses. Furthermore, we identified some tRNA-derived fragments associated with Entamoeba Argonaute proteins, EhAgo2-2 and EhAgo2-3, which have a preference for different tRNA-derived fragment species. Finally, we show that tRNA halves are packaged inside extracellular vesicles secreted by amoebas. The ubiquitous presence of tRNA-derived fragments, their association with the Argonaute proteins, and the accumulation of tRNA halves during multiple different stresses, including encystation, suggest a nuanced level of gene expression regulation mediated by different tRNA-derived fragments in Entamoeba. American Society for Microbiology 2023-02-21 /pmc/articles/PMC10127584/ /pubmed/36809068 http://dx.doi.org/10.1128/mbio.03450-22 Text en https://doi.org/10.1128/AuthorWarrantyLicense.v1This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. |
spellingShingle | Research Article Sharma, Manu Zhang, Hanbang Ehrenkaufer, Gretchen Singh, Upinder Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves |
title | Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves |
title_full | Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves |
title_fullStr | Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves |
title_full_unstemmed | Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves |
title_short | Stress Response in Entamoeba histolytica Is Associated with Robust Processing of tRNA to tRNA Halves |
title_sort | stress response in entamoeba histolytica is associated with robust processing of trna to trna halves |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127584/ https://www.ncbi.nlm.nih.gov/pubmed/36809068 http://dx.doi.org/10.1128/mbio.03450-22 |
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