EGFR modulates microRNA maturation in response to hypoxia through phosphorylation of AGO2 (original) (raw)

• Letter
• Published: 01 May 2013
• Weiya Xia1,
• Yekaterina B. Khotskaya1,
• Longfei Huo1,
• Kotaro Nakanishi3,
• Seung-Oe Lim1,
• Yi Du1,2,
• Yan Wang1,
• Wei-Chao Chang4,5,
• Chung-Hsuan Chen5,
• Jennifer L. Hsu1,4,6,
• Yun Wu7,
• Yung Carmen Lam1,
• Brian P. James8,
• Xiuping Liu8,
• Chang-Gong Liu8,
• Dinshaw J. Patel3 &
• …
• Mien-Chie Hung1,2,4,6

Nature volume 497, pages 383–387 (2013)Cite this article

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Abstract

MicroRNAs (miRNAs) are generated by two-step processing to yield small RNAs that negatively regulate target gene expression at the post-transcriptional level1. Deregulation of miRNAs has been linked to diverse pathological processes, including cancer2,3. Recent studies have also implicated miRNAs in the regulation of cellular response to a spectrum of stresses4, such as hypoxia, which is frequently encountered in the poorly angiogenic core of a solid tumour5. However, the upstream regulators of miRNA biogenesis machineries remain obscure, raising the question of how tumour cells efficiently coordinate and impose specificity on miRNA expression and function in response to stresses. Here we show that epidermal growth factor receptor (EGFR), which is the product of a well-characterized oncogene in human cancers, suppresses the maturation of specific tumour-suppressor-like miRNAs in response to hypoxic stress through phosphorylation of argonaute 2 (AGO2) at Tyr 393. The association between EGFR and AGO2 is enhanced by hypoxia, leading to elevated AGO2-Y393 phosphorylation, which in turn reduces the binding of Dicer to AGO2 and inhibits miRNA processing from precursor miRNAs to mature miRNAs. We also identify a long-loop structure in precursor miRNAs as a critical regulatory element in phospho-Y393-AGO2-mediated miRNA maturation. Furthermore, AGO2-Y393 phosphorylation mediates EGFR-enhanced cell survival and invasiveness under hypoxia, and correlates with poorer overall survival in breast cancer patients. Our study reveals a previously unrecognized function of EGFR in miRNA maturation and demonstrates how EGFR is likely to function as a regulator of AGO2 through novel post-translational modification. These findings suggest that modulation of miRNA biogenesis is important for stress response in tumour cells and has potential clinical implications.

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Acknowledgements

We thank B. Pickering, D. Yu, and A.-B. Shyu for suggestions and technical assistance with northern blot analysis. This work was supported by the US National Institutes of Health (CA109311 and CA099031 to M.-C.H., and CCSG Core Grant CA16672), the US National Breast Cancer Foundation, The Center for Biological Pathway at the UT MD Anderson Cancer Center, S. G. Komen (SAC110016 to M.-C.H.), The Sister Institution Fund of China Medical University and Hospital and the UT MD Anderson Cancer Center, the Cancer Research Center of Excellence (D0H102-TD-C-111-005, Taiwan), a Private University grant (NSC99-2632-B-039-001-MY3, Taiwan), and the Program for Stem Cell and Regenerative Medicine Frontier Research (NSC101-2321-B-039-001, Taiwan).

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Authors and Affiliations

1. Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA,
   Jia Shen, Weiya Xia, Yekaterina B. Khotskaya, Longfei Huo, Seung-Oe Lim, Yi Du, Yan Wang, Jennifer L. Hsu, Yung Carmen Lam & Mien-Chie Hung
2. The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, 77030, Texas, USA
   Jia Shen, Yi Du & Mien-Chie Hung
3. Structural Biology Program, Memorial Sloan-Kettering Cancer Center, New York, 10065, New York, USA
   Kotaro Nakanishi & Dinshaw J. Patel
4. Center for Molecular Medicine and Graduate Institute of Cancer Biology, China Medical University, Taichung 402, Taiwan
   Wei-Chao Chang, Jennifer L. Hsu & Mien-Chie Hung
5. Genomics Research Center, Academia Sinica, Nankang, 105, Taipei, Taiwan
   Wei-Chao Chang & Chung-Hsuan Chen
6. Asia University, Taichung, 413, Taiwan
   Jennifer L. Hsu & Mien-Chie Hung
7. Department of Pathology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA,
   Yun Wu
8. Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA,
   Brian P. James, Xiuping Liu & Chang-Gong Liu

Authors

1. Jia Shen
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2. Weiya Xia
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3. Yekaterina B. Khotskaya
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4. Longfei Huo
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5. Kotaro Nakanishi
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6. Seung-Oe Lim
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7. Yi Du
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8. Yan Wang
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9. Wei-Chao Chang
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10. Chung-Hsuan Chen
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11. Jennifer L. Hsu
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12. Yun Wu
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13. Yung Carmen Lam
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14. Brian P. James
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15. Xiuping Liu
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16. Chang-Gong Liu
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17. Dinshaw J. Patel
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18. Mien-Chie Hung
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Contributions

J.S. and M.-C.H. designed and conceived the study; J.S. and M.-C.H. wrote the manuscript; J.L.H. contributed to the preparation of the manuscript. J.S., W.X., Y.B.K., L.H., S.-O.L., Y.D., Y. Wang, W.-C.C. and C.-H.C. did the experiments; Y. Wu provided human primary breast tumour samples; Y.C.L. provided the split-half-YFP-fused constructs; X.L. and C.-G.L. assisted in next-generation RNA deep sequencing; B.P.J. provided the pipeline analysis service for RNA sequencing data; and K.N. and D.-J.P. analysed the crystal structure of human AGO2.

Corresponding author

Correspondence toMien-Chie Hung.

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The authors declare no competing financial interests.

Supplementary information

Supplementary Information

This file contains Supplementary Figures 1–41, Supplementary Table 1, Supplementary Methods and Supplementary References. (PDF 15146 kb)

Supplementary Data

This file contains the Normalized Expression (RPKM) of mRNAs that are regulated by EGFR and likely to be targeted by Top-Scoring mHESM. (XLS 68 kb)

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Shen, J., Xia, W., Khotskaya, Y. et al. EGFR modulates microRNA maturation in response to hypoxia through phosphorylation of AGO2.Nature 497, 383–387 (2013). https://doi.org/10.1038/nature12080

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• Received: 12 January 2012
• Accepted: 19 March 2013
• Published: 01 May 2013
• Issue Date: 16 May 2013
• DOI: https://doi.org/10.1038/nature12080

Editorial Summary

Impact of hypoxia on miRNAs

MicroRNA-mediated regulation of gene expression occurs during response to stresses such as hypoxia, a condition found in the centre of a solid tumour. Mien-Chie Hung and colleagues show that the oncogene product EGFR (epidermal growth factor receptor) phosphorylates argonaute 2 (AGO2), a critical factor in the biogenesis of microRNAs, and that this process is enhanced by hypoxia. This modification of AGO2 impairs microRNA processing, but promotes cell survival and invasiveness. Breast cancer patients with higher phospho-AGO2 content show a poorer outcome.