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Updated: Apr 12, 2026

Rapid Generation of Primary Murine Melanocyte and Fibroblast Cultures
Published on: June 26, 2019
MiR-191 Regulates Primary Human Fibroblast Proliferation and Directly Targets Multiple Oncogenes
Damon Polioudakis1, Nathan S Abell1, Vishwanath R Iyer1
1Center for Systems and Synthetic Biology, Institute for Cellular and Molecular Biology, Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, United States of America.
Abstract:
miRNAs play a central role in numerous pathologies including multiple cancer types. miR-191 has predominantly been studied as an oncogene, but the role of miR-191 in the proliferation of primary cells is not well characterized, and the miR-191 targetome has not been experimentally profiled. Here we utilized RNA induced silencing complex immunoprecipitations as well as gene expression profiling to construct a genome wide miR-191 target profile. We show that miR-191 represses proliferation in primary human fibroblasts, identify multiple proto-oncogenes as novel miR-191 targets, including CDK9, NOTCH2, and RPS6KA3, and present evidence that miR-191 extensively mediates target expression through coding sequence (CDS) pairing. Our results provide a comprehensive genome wide miR-191 target profile, and demonstrate miR-191's regulation of primary human fibroblast proliferation.
Insights
MicroRNA-191 (miR-191) represses proliferation in human fibroblasts. This study identifies novel proto-oncogene targets of miR-191, revealing its complex role in cell growth.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- MicroRNAs (miRNAs) are key regulators in various diseases, including cancers.
- miR-191 is often considered an oncogene, but its function in primary cell proliferation and its full targetome are not well understood.
Purpose of the Study:
- To construct a comprehensive, genome-wide miR-191 target profile.
- To investigate the role of miR-191 in the proliferation of primary human fibroblasts.
Main Methods:
- RNA-induced silencing complex (RISC) immunoprecipitations.
- Gene expression profiling.
- Bioinformatic analysis to identify miR-191 targets.
Main Results:
- A genome-wide miR-191 target profile was established.
- miR-191 was found to repress proliferation in primary human fibroblasts.
- Novel miR-191 targets, including proto-oncogenes CDK9, NOTCH2, and RPS6KA3, were identified.
- Evidence suggests miR-191 primarily targets the coding sequence (CDS) of its targets.
Conclusions:
- miR-191 plays a significant role in regulating primary human fibroblast proliferation.
- The identified miR-191 targets and mechanisms provide new insights into miR-191's function in cellular processes and disease.
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