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mRNA Decay Mediated by Two Distinct AU-Rich Elements from c- fos and Granulocyte-Macrophage Colony-Stimulating Factor Transcripts: Different Deadenylation Kinetics and Uncoupling from Translation
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Binding of destabilizing RBPs to AREs results in recruitment of deadenylases, leading to rapid deadenylation, decapping, and ultimately degradation of the target mRNA.
“The binding of destabilizing RBPs to the AREs results in recruitment of deadenylases, leading to rapid deadenylation, decapping, and ultimately degradation of the target mRNA [28].”
From The low-density lipoprotein receptor: Emerging post-transcriptional regulatory mechanisms (2025) · cites this paper as [28]
The Abstract reports that c-fos and GM-CSF AREs direct rapid deadenylation as the first step in mRNA degradation. The Discussion proposes that ARE-associated RNA–protein complexes could recruit RNases, but presents recruitment as a possible mechanism, not an established result. It describes subsequent degradation by exonuclease or endonuclease and does not establish the claimed decapping step. Page numbers were not supplied for these passages. (LLM, conf=0.88)
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Tsai, K.-C., Cansino, V. V., Kohn, D. T., Neve, R. L., & Perrone-Bizzozero, N. I. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-06-01950.1997 · Cited by 66
Inflammation and survival pathways: Chronic lymphocytic leukemia as a model system
Chen, L. S., Balakrishnan, K., & Gandhi, V. (2010) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.07.039 · Cited by 55
The low-density lipoprotein receptor: Emerging post-transcriptional regulatory mechanisms
Ndoj, K., Meurs, A., Papaioannou, D., Bjune, K., & Zelcer, N. (2025) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2024.119082 · Cited by 17
Metadata
- Authors
- Chen, C.-Y. A., Xu, N., & Shyu, A.-B.
- Affiliations
- Department of Biochemistry and Molecular Biology, Medical School, The University of Texas Houston Health Science Center
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 1995-10
- Volume
- 15
- Issue
- 10
- Pages
- 5777-5788
- ISSN
- 1098-5549
- Cited by
- 231
- References
- 0
- Language
- en
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