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RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs

Hypoxia-inducible factor 1α (HIF1α) is a transcription factor that regulates angiogenesis under hypoxic conditions. To investigate the posttranscriptional regulatory mechanism of HIF1α, we performed a cell-based screening to reveal potential cis-elements and the regulatory RNA-binding proteins that...

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Autores principales: Yamamoto, Hiroto, Uchida, Yutaro, Kurimoto, Ryota, Chiba, Tomoki, Matsushima, Takahide, Ito, Yoshiaki, Inotsume, Maiko, Miyata, Kohei, Watanabe, Kenta, Inada, Masaki, Goshima, Naoki, Uchida, Tokujiro, Asahara, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823215/
https://www.ncbi.nlm.nih.gov/pubmed/36509142
http://dx.doi.org/10.1016/j.jbc.2022.102791
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author Yamamoto, Hiroto
Uchida, Yutaro
Kurimoto, Ryota
Chiba, Tomoki
Matsushima, Takahide
Ito, Yoshiaki
Inotsume, Maiko
Miyata, Kohei
Watanabe, Kenta
Inada, Masaki
Goshima, Naoki
Uchida, Tokujiro
Asahara, Hiroshi
author_facet Yamamoto, Hiroto
Uchida, Yutaro
Kurimoto, Ryota
Chiba, Tomoki
Matsushima, Takahide
Ito, Yoshiaki
Inotsume, Maiko
Miyata, Kohei
Watanabe, Kenta
Inada, Masaki
Goshima, Naoki
Uchida, Tokujiro
Asahara, Hiroshi
author_sort Yamamoto, Hiroto
collection PubMed
description Hypoxia-inducible factor 1α (HIF1α) is a transcription factor that regulates angiogenesis under hypoxic conditions. To investigate the posttranscriptional regulatory mechanism of HIF1α, we performed a cell-based screening to reveal potential cis-elements and the regulatory RNA-binding proteins that act as trans-factors. We found that LIN28A promoted HIF1α protein expression independently of the downregulation of microRNA let-7, which is also directly mediated by LIN28A. Transcriptome analysis and evaluation of RNA stability using RNA-seq and SLAM-seq analyses, respectively, revealed that LIN28A upregulates HIF1A expression via mRNA stabilization. To investigate the physical association of LIN28A with HIF1A mRNA, we performed enhanced crosslinking immunoprecipitation in 293FT cells and integrally analyzed the transcriptome. We observed that LIN28A associates with HIF1A mRNA via its cis-element motif “UGAU”. The “UGAU” motifs are recognized by the cold shock domain of LIN28A, and the introduction of a loss-of-function mutation to the cold shock domain diminished the upregulatory activities performed by LIN28A. Finally, the microvessel density assay showed that the expression of LIN28A promoted angiogenesis in vivo. In conclusion, our study elucidated the role of LIN28A in enhancing the HIF1α axis at the posttranscription layer.
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spelling pubmed-98232152023-01-09 RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs Yamamoto, Hiroto Uchida, Yutaro Kurimoto, Ryota Chiba, Tomoki Matsushima, Takahide Ito, Yoshiaki Inotsume, Maiko Miyata, Kohei Watanabe, Kenta Inada, Masaki Goshima, Naoki Uchida, Tokujiro Asahara, Hiroshi J Biol Chem JBC Communication Hypoxia-inducible factor 1α (HIF1α) is a transcription factor that regulates angiogenesis under hypoxic conditions. To investigate the posttranscriptional regulatory mechanism of HIF1α, we performed a cell-based screening to reveal potential cis-elements and the regulatory RNA-binding proteins that act as trans-factors. We found that LIN28A promoted HIF1α protein expression independently of the downregulation of microRNA let-7, which is also directly mediated by LIN28A. Transcriptome analysis and evaluation of RNA stability using RNA-seq and SLAM-seq analyses, respectively, revealed that LIN28A upregulates HIF1A expression via mRNA stabilization. To investigate the physical association of LIN28A with HIF1A mRNA, we performed enhanced crosslinking immunoprecipitation in 293FT cells and integrally analyzed the transcriptome. We observed that LIN28A associates with HIF1A mRNA via its cis-element motif “UGAU”. The “UGAU” motifs are recognized by the cold shock domain of LIN28A, and the introduction of a loss-of-function mutation to the cold shock domain diminished the upregulatory activities performed by LIN28A. Finally, the microvessel density assay showed that the expression of LIN28A promoted angiogenesis in vivo. In conclusion, our study elucidated the role of LIN28A in enhancing the HIF1α axis at the posttranscription layer. American Society for Biochemistry and Molecular Biology 2022-12-09 /pmc/articles/PMC9823215/ /pubmed/36509142 http://dx.doi.org/10.1016/j.jbc.2022.102791 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle JBC Communication
Yamamoto, Hiroto
Uchida, Yutaro
Kurimoto, Ryota
Chiba, Tomoki
Matsushima, Takahide
Ito, Yoshiaki
Inotsume, Maiko
Miyata, Kohei
Watanabe, Kenta
Inada, Masaki
Goshima, Naoki
Uchida, Tokujiro
Asahara, Hiroshi
RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs
title RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs
title_full RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs
title_fullStr RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs
title_full_unstemmed RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs
title_short RNA-binding protein LIN28A upregulates transcription factor HIF1α by posttranscriptional regulation via direct binding to UGAU motifs
title_sort rna-binding protein lin28a upregulates transcription factor hif1α by posttranscriptional regulation via direct binding to ugau motifs
topic JBC Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823215/
https://www.ncbi.nlm.nih.gov/pubmed/36509142
http://dx.doi.org/10.1016/j.jbc.2022.102791
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