MicroRNA MiR-17 retards tissue growth and represses fibronectin expression

Sze Wan Shan, Daniel Y. Lee, Zhaoqun Deng, Tatiana Shatseva, Zina Jeyapalan, William W. Du, Yaou Zhang, Jim W. Xuan, Siu Pok Yee, Vinayakumar Siragam, Burton B. Yang

Research output: Journal article publicationJournal articleAcademic researchpeer-review

175 Citations (Scopus)

Abstract

MicroRNAs (miRNAs) are single-stranded regulatory RNAs, frequently expressed as clusters. Previous studies have demonstrated that the six-miRNA cluster miR-17∼92 has important roles in tissue development and cancers. However, the precise role of each miRNA in the cluster is unknown. Here we show that overexpression of miR-17 results in decreased cell adhesion, migration and proliferation. Transgenic mice overexpressing miR-17 showed overall growth retardation, smaller organs and greatly reduced haematopoietic cell lineages. We found that fibronectin and the fibronectin type-III domain containing 3A (FNDC3A) are two targets that have their expression repressed by miR-17, both in vitro and in transgenic mice. Several lines of evidence support the notion that miR-17 causes cellular defects through its repression of fibronectin expression. Our single miRNA expression assay may be evolved to allow the manipulation of individual miRNA functions in vitro and in vivo. We anticipate that this could serve as a model for studying gene regulation by miRNAs in the development of gene therapy.

Original languageEnglish
Pages (from-to)1031-1038
Number of pages8
JournalNature Cell Biology
Volume11
Issue number8
DOIs
Publication statusPublished - 2009
Externally publishedYes

ASJC Scopus subject areas

  • Cell Biology

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