AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation
In the present study, we investigated the 3′ untranslated region (UTR) of the mouse core clock gene cryptochrome 1 (Cry1) at the post-transcriptional level, particularly its translational regulation. Interestingly, the 3′UTR of Cry1 mRNA decreased its mRNA levels but increased protein amounts. The 3...
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pubmed-39733352014-04-04 AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation Lee, Kyung-Ha Kim, Sung-Hoon Kim, Hyo-Jin Kim, Wanil Lee, Hwa-Rim Jung, Youngseob Choi, Jung-Hyun Hong, Ka Young Jang, Sung Key Kim, Kyong-Tai Gene Regulation, Chromatin and Epigenetics In the present study, we investigated the 3′ untranslated region (UTR) of the mouse core clock gene cryptochrome 1 (Cry1) at the post-transcriptional level, particularly its translational regulation. Interestingly, the 3′UTR of Cry1 mRNA decreased its mRNA levels but increased protein amounts. The 3′UTR is widely known to function as a cis-acting element of mRNA degradation. The 3′UTR also provides a binding site for microRNA and mainly suppresses translation of target mRNAs. We found that AU-rich element RNA binding protein 1 (AUF1) directly binds to the Cry1 3′UTR and regulates translation of Cry1 mRNA. AUF1 interacted with eukaryotic translation initiation factor 3 subunit B and also directly associated with ribosomal protein S3 or ribosomal protein S14, resulting in translation of Cry1 mRNA in a 3′UTR-dependent manner. Expression of cytoplasmic AUF1 and binding of AUF1 to the Cry1 3′UTR were parallel to the circadian CRY1 protein profile. Our results suggest that the 3′UTR of Cry1 is important for its rhythmic translation, and AUF1 bound to the 3′UTR facilitates interaction with the 5′ end of mRNA by interacting with translation initiation factors and recruiting the 40S ribosomal subunit to initiate translation of Cry1 mRNA. Oxford University Press 2014-04 2014-01-13 /pmc/articles/PMC3973335/ /pubmed/24423872 http://dx.doi.org/10.1093/nar/gkt1379 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
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Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
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NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Lee, Kyung-Ha Kim, Sung-Hoon Kim, Hyo-Jin Kim, Wanil Lee, Hwa-Rim Jung, Youngseob Choi, Jung-Hyun Hong, Ka Young Jang, Sung Key Kim, Kyong-Tai |
spellingShingle |
Lee, Kyung-Ha Kim, Sung-Hoon Kim, Hyo-Jin Kim, Wanil Lee, Hwa-Rim Jung, Youngseob Choi, Jung-Hyun Hong, Ka Young Jang, Sung Key Kim, Kyong-Tai AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation |
author_facet |
Lee, Kyung-Ha Kim, Sung-Hoon Kim, Hyo-Jin Kim, Wanil Lee, Hwa-Rim Jung, Youngseob Choi, Jung-Hyun Hong, Ka Young Jang, Sung Key Kim, Kyong-Tai |
author_sort |
Lee, Kyung-Ha |
title |
AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation |
title_short |
AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation |
title_full |
AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation |
title_fullStr |
AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation |
title_full_unstemmed |
AUF1 contributes to Cryptochrome1 mRNA degradation and rhythmic translation |
title_sort |
auf1 contributes to cryptochrome1 mrna degradation and rhythmic translation |
description |
In the present study, we investigated the 3′ untranslated region (UTR) of the mouse core clock gene cryptochrome 1 (Cry1) at the post-transcriptional level, particularly its translational regulation. Interestingly, the 3′UTR of Cry1 mRNA decreased its mRNA levels but increased protein amounts. The 3′UTR is widely known to function as a cis-acting element of mRNA degradation. The 3′UTR also provides a binding site for microRNA and mainly suppresses translation of target mRNAs. We found that AU-rich element RNA binding protein 1 (AUF1) directly binds to the Cry1 3′UTR and regulates translation of Cry1 mRNA. AUF1 interacted with eukaryotic translation initiation factor 3 subunit B and also directly associated with ribosomal protein S3 or ribosomal protein S14, resulting in translation of Cry1 mRNA in a 3′UTR-dependent manner. Expression of cytoplasmic AUF1 and binding of AUF1 to the Cry1 3′UTR were parallel to the circadian CRY1 protein profile. Our results suggest that the 3′UTR of Cry1 is important for its rhythmic translation, and AUF1 bound to the 3′UTR facilitates interaction with the 5′ end of mRNA by interacting with translation initiation factors and recruiting the 40S ribosomal subunit to initiate translation of Cry1 mRNA. |
publisher |
Oxford University Press |
publishDate |
2014 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973335/ |
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1612073363389284352 |