Miles A. Whittington, Ian M. Stanford, et al.
Journal of Physiology
MicroRNA (miRNA) are a class of non-coding RNA that suppress gene expression by degradation or translational inhibition of target RNA. Several miRNA have been shown to target oncogenes and recently miRNA-125b was shown to translationally and transcriptionally inhibit the p53 gene. Here, we show that an additional isomer of miRNA-125 (miRNA-125a) translationally arrests mRNA of the p53 tumor suppressor gene. The basis of this activity is the high degree of sequence homology between the seed sequence of miR-125a and the 3′-UTR of p53. Our findings add miRNA-125a to the growing list of miRNA with oncogenic targets. © 2009 Federation of European Biochemical Societies.
Miles A. Whittington, Ian M. Stanford, et al.
Journal of Physiology
Amol Thakkar, Andrea Antonia Byekwaso, et al.
ACS Fall 2022
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ACS Fall 2023
John M. Prager, Jennifer J. Liang, et al.
AMIA Joint Summits on Translational Science 2017