The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications]
Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M.
Cold Spring Harbor Laboratory Press
Published 2018
Cold Spring Harbor Laboratory Press
Published 2018
Publication Date: |
2018-10-02
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Publisher: |
Cold Spring Harbor Laboratory Press
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Print ISSN: |
0890-9369
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Topics: |
Biology
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Published by: |
_version_ | 1836399060887535616 |
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autor | Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. |
beschreibung | MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors. |
citation_standardnr | 6339451 |
datenlieferant | ipn_articles |
feed_id | 1644 |
feed_publisher | Cold Spring Harbor Laboratory Press |
feed_publisher_url | http://www.cshlpress.com/ |
insertion_date | 2018-10-02 |
journalissn | 0890-9369 |
publikationsjahr_anzeige | 2018 |
publikationsjahr_facette | 2018 |
publikationsjahr_intervall | 7984:2015-2019 |
publikationsjahr_sort | 2018 |
publisher | Cold Spring Harbor Laboratory Press |
quelle | Genes & Development |
relation | http://genesdev.cshlp.org/cgi/content/short/32/19-20/1303?rss=1 |
search_space | articles |
shingle_author_1 | Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. |
shingle_author_2 | Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. |
shingle_author_3 | Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. |
shingle_author_4 | Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. |
shingle_catch_all_1 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors. Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. Cold Spring Harbor Laboratory Press 0890-9369 08909369 |
shingle_catch_all_2 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors. Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. Cold Spring Harbor Laboratory Press 0890-9369 08909369 |
shingle_catch_all_3 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors. Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. Cold Spring Harbor Laboratory Press 0890-9369 08909369 |
shingle_catch_all_4 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors. Lafita-Navarro, M. C., Kim, M., Borenstein-Auerbach, N., Venkateswaran, N., Hao, Y.-H., Ray, R., Brabletz, T., Scaglioni, P. P., Shay, J. W., Conacci-Sorrell, M. Cold Spring Harbor Laboratory Press 0890-9369 08909369 |
shingle_title_1 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] |
shingle_title_2 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] |
shingle_title_3 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] |
shingle_title_4 | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] |
timestamp | 2025-06-30T23:36:58.692Z |
titel | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] |
titel_suche | The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells [Research Communications] |
topic | W |
uid | ipn_articles_6339451 |