4.5 Review

The miR-29 family: genomics, cell biology, and relevance to renal and cardiovascular injury

Journal

PHYSIOLOGICAL GENOMICS
Volume 44, Issue 4, Pages 237-244

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00141.2011

Keywords

microRNA; kidney; heart

Funding

  1. US National Institutes of Health [HL-085267, DK-084405, HL-082798, HL-029587]
  2. Clinical and Translational Science Institute
  3. National Natural Science Foundation of China [30871176, 30971374]

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Kriegel AJ, Fang YL, Ding X, Liang M. The miR-29 family: genomics, cell biology, and relevance to renal and cardiovascular injury. Physiol Genomics 44: 237-244, 2012. First published January 3, 2012; doi:10.1152/physiolgenomics.00141.2011.-The human miR-29 family of microRNAs has three mature members, miR-29a, miR-29b, and miR-29c. miR-29s are encoded by two gene clusters. Binding sites for several transcriptional factors have been identified in the promoter regions of miR-29 genes. The miR-29 family members share a common seed region sequence and are predicted to target largely overlapping sets of genes. However, the miR-29 family members exhibit differential regulation in several cases and different subcellular distribution, suggesting their functional relevance may not be identical. miR-29s directly target at least 16 extracellular matrix genes, providing a dramatic example of a single microRNA targeting a large group of functionally related genes. Strong antifibrotic effects of miR-29s have been demonstrated in heart, kidney, and other organs. miR-29s have also been shown to be proapoptotic and involved in the regulation of cell differentiation. It remains to be explored how various cellular effects of miR-29s determine functional relevance of miR-29s to specific diseases and how the miR-29 family members may function cooperatively or separately.

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