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Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression

The mouse PERIOD1 (mPER1) plays an important role in the maintenance of circadian rhythm. Translation of mPer1 is directed by both a cap-dependent process and cap-independent translation mediated by an internal ribosomal entry site (IRES) in the 5′ untranslated region (UTR). Here, we compared mPer1...

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Autores principales: Lee, Kyung-Ha, Kim, Sung-Hoon, Kim, Do-Yeon, Kim, Seunghwan, Kim, Kyong-Tai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360671/
https://www.ncbi.nlm.nih.gov/pubmed/22662251
http://dx.doi.org/10.1371/journal.pone.0037936
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author Lee, Kyung-Ha
Kim, Sung-Hoon
Kim, Do-Yeon
Kim, Seunghwan
Kim, Kyong-Tai
author_facet Lee, Kyung-Ha
Kim, Sung-Hoon
Kim, Do-Yeon
Kim, Seunghwan
Kim, Kyong-Tai
author_sort Lee, Kyung-Ha
collection PubMed
description The mouse PERIOD1 (mPER1) plays an important role in the maintenance of circadian rhythm. Translation of mPer1 is directed by both a cap-dependent process and cap-independent translation mediated by an internal ribosomal entry site (IRES) in the 5′ untranslated region (UTR). Here, we compared mPer1 IRES activity with other cellular IRESs. We also found critical region in mPer1 5′UTR for heterogeneous nuclear ribonucleoprotein Q (HNRNPQ) binding. Deletion of HNRNPQ binding region markedly decreased IRES activity and disrupted rhythmicity. A mathematical model also suggests that rhythmic IRES-dependent translation is a key process in mPER1 oscillation. The IRES-mediated translation of mPer1 will help define the post-transcriptional regulation of the core clock genes.
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spelling pubmed-33606712012-06-01 Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression Lee, Kyung-Ha Kim, Sung-Hoon Kim, Do-Yeon Kim, Seunghwan Kim, Kyong-Tai PLoS One Research Article The mouse PERIOD1 (mPER1) plays an important role in the maintenance of circadian rhythm. Translation of mPer1 is directed by both a cap-dependent process and cap-independent translation mediated by an internal ribosomal entry site (IRES) in the 5′ untranslated region (UTR). Here, we compared mPer1 IRES activity with other cellular IRESs. We also found critical region in mPer1 5′UTR for heterogeneous nuclear ribonucleoprotein Q (HNRNPQ) binding. Deletion of HNRNPQ binding region markedly decreased IRES activity and disrupted rhythmicity. A mathematical model also suggests that rhythmic IRES-dependent translation is a key process in mPER1 oscillation. The IRES-mediated translation of mPer1 will help define the post-transcriptional regulation of the core clock genes. Public Library of Science 2012-05-25 /pmc/articles/PMC3360671/ /pubmed/22662251 http://dx.doi.org/10.1371/journal.pone.0037936 Text en Lee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lee, Kyung-Ha
Kim, Sung-Hoon
Kim, Do-Yeon
Kim, Seunghwan
Kim, Kyong-Tai
Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression
title Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression
title_full Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression
title_fullStr Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression
title_full_unstemmed Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression
title_short Internal Ribosomal Entry Site-Mediated Translation Is Important for Rhythmic PERIOD1 Expression
title_sort internal ribosomal entry site-mediated translation is important for rhythmic period1 expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360671/
https://www.ncbi.nlm.nih.gov/pubmed/22662251
http://dx.doi.org/10.1371/journal.pone.0037936
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