Alternative Polyadenylation Allows Differential Negative Feedback of Human miRNA miR-579 on Its Host Gene ZFR

• Published in: PloS one Vol. 10; no. 3; p. e0121507
• Main Authors: Hinske, Ludwig Christian, Galante, Pedro A. F., Limbeck, Elisabeth, Möhnle, Patrick, Parmigiani, Raphael B., Ohno-Machado, Lucila, Camargo, Anamaria A., Kreth, Simone
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 23.03.2015; Public Library of Science (PLoS)
• Subjects: Acids; Analysis; Anesthesiology; Binding sites; Bioinformatics; Biological effects; Cell Line, Tumor; Cleavage And Polyadenylation Specificity Factor - genetics; Computational Biology; Control methods; Control theory; Crosstalk; Encyclopedias; Feedback; Feedback loops; Feedback, Physiological; Gene expression; Gene Expression Regulation - genetics; Genes; Genomes; Genomics; Humans; Introns - genetics; MicroRNA; MicroRNAs; MicroRNAs - genetics; miRNA; Molecular biology; Negative feedback; Oncology; Ontology; Polyadenylation; Proteins; Ribonucleic acid; RNA; RNA-Binding Proteins - genetics; Signal transduction; Transcription; England; Brazil; California; United Kingdom > UK; United States > US; Germany
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0121507

About half of the known miRNA genes are located within protein-coding host genes, and are thus subject to co-transcription. Accumulating data indicate that this coupling may be an intrinsic mechanism to directly regulate the host gene's expression, constituting a negative feedback loop. Inevitably, the cell requires a yet largely unknown repertoire of methods to regulate this control mechanism. We propose APA as one possible mechanism by which negative feedback of intronic miRNA on their host genes might be regulated. Using in-silico analyses, we found that host genes that contain seed matching sites for their intronic miRNAs yield longer 32UTRs with more polyadenylation sites. Additionally, the distribution of polyadenylation signals differed significantly between these host genes and host genes of miRNAs that do not contain potential miRNA binding sites. We then transferred these in-silico results to a biological example and investigated the relationship between ZFR and its intronic miRNA miR-579 in a U87 cell line model. We found that ZFR is targeted by its intronic miRNA miR-579 and that alternative polyadenylation allows differential targeting. We additionally used bioinformatics analyses and RNA-Seq to evaluate a potential cross-talk between intronic miRNAs and alternative polyadenylation. CPSF2, a gene previously associated with alternative polyadenylation signal recognition, might be linked to intronic miRNA negative feedback by altering polyadenylation signal utilization.