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Reversible HuR‐microRNA binding controls extracellular export of miR‐122 and augments stress response
Abstract
microRNAs (miRNAs), the tiny but stable regulatory RNAs in metazoan cells, can undergo selective turnover in presence of specific internal and external cues to control cellular response against the changing environment. We have observed reduction in cellular miR‐122 content, due to their accelerated extracellular export in human hepatic cells starved for small metabolites including amino acids. In this context, a new role of human ELAV protein HuR has been identified. HuR, a negative regulator of miRNA function, accelerates extracellular vesicle (EV)‐mediated export of miRNAs in human cells. In stressed cells, HuR replaces miRNPs from target messages and is both necessary and sufficient for the extracellular export of corresponding miRNAs. HuR could reversibly bind miRNAs to replace them from Ago2 and subsequently itself gets freed from bound miRNAs upon ubiquitination. The ubiquitinated form of HuR is predominantly associated with multivesicular bodies (MVB) where HuR‐unbound miRNAs also reside. These MVB‐associated pool of miRNAs get exported out via EVs thereby delimiting cellular miR‐122 level during starvation. Therefore, by modulating extracellular export of miR‐122, HuR could control stress response in starved human hepatic cells.
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“Several RNA-binding proteins have been identified to be associated with selective packaging of miR-122, including lupus La protein [63] and human ELAV protein HuR under stress, both verified in human cell lines [64].”
From Differential RNA packaging into small extracellular vesicles by neurons and astrocytes (2021) · cites this paper as [64]
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Metadata
- Authors
- Mukherjee, K., Ghoshal, B., Ghosh, S., Chakrabarty, Y., Shwetha, S., Das, S., & Bhattacharyya, S. N.
- Venue
- The EMBO Reports
- Published
- 2016-07-11
- Volume
- 17
- Issue
- 8
- Pages
- 1184-1203
- ISSN
- 1469-221X
- 1469-3178
- PMC
- PMC4967961
- Cited by
- 184
- References
- 3
- Language
- en
- Funders
- HFSPO Career Development Fund (CDA‐25/2007‐C)
- Wellcome Trust (084324/Z/07/A)
- Lady Tata Memorial Trust (YRA‐2009)
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