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The RNAbinding protein AUF1 binds AUrich elements in 3'untranslated regions to regulate mRNA degradation and/or translation. Many of these mRNAs are predicted microRNA targets as well. An emerging theme in posttranscriptional control of gene expression is that RNAbinding proteins and microRNAs coregulate mRNAs. Recent experiments and bioinformatic analyses suggest this type of coregulation may be widespread across the transcriptome. Here, we identified mRNA targets of AUF1 from a complex pool of cellular mRNAs and examined a subset of these mRNAs to explore the links between RNA binding and mRNA degradation for Insanity Workout
both AUF1 and Argonaute 2 (AGO2), which is an essential effector of microRNAinduced gene silencing. Depending on the specific mRNA examined, AUF1 and AGO2 binding is proportional/cooperative, reciprocal/competitive or independent. For most mRNAs in which AUF1 affects their decay rates, mRNA degradation requires AGO2. Thus, AUF1 and AGO2 present mRNAspecific allosteric binding relationships for coregulation of mRNA degradation.