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https://doi.org/10.1186/s12944-015-0163-6
Title: | DDX5/p68 RNA helicase expression is essential for initiating adipogenesis | Authors: | Ramanathan, N Lim, N Stewart, C.L |
Keywords: | DEAD box protein 5 nuclear factor unclassified drug Ddx5 protein, mouse DEAD box protein adipocyte adipogenesis animal cell Article cell differentiation cell viability controlled study Ddx5 gene gene gene expression gene function gene repression nonhuman protein expression RNA isolation 3T3-L1 cell line animal C3H mouse enzymology gene silencing genetics mesenchymal stroma cell metabolism mouse physiology 3T3-L1 Cells Adipocytes Adipogenesis Animals DEAD-box RNA Helicases Gene Expression Gene Knockdown Techniques Mesenchymal Stromal Cells Mice Mice, Inbred C3H |
Issue Date: | 2015 | Citation: | Ramanathan, N, Lim, N, Stewart, C.L (2015). DDX5/p68 RNA helicase expression is essential for initiating adipogenesis. Lipids in Health and Disease 14 (1) : 160. ScholarBank@NUS Repository. https://doi.org/10.1186/s12944-015-0163-6 | Rights: | Attribution 4.0 International | Abstract: | Background: DDX5/p68 RNA helicase is a member of the DEAD (Asp-Glu-Ala-Asp) box proteins. Apart from RNA unwinding, DDX5 is an important transcriptional factor and co-activator in cell proliferation and differentiation. Findings: Here, we have characterised the role of DDX5 in adipogenesis in 3T3-L1 cells using siRNA mediated suppression. Transient inhibition of Ddx5 mRNA expression at the start of adipogenesis impairs the differentiation programme even when DDX5 expression is restored later in adipogenesis. However transient suppression of Ddx5 at the later stages of adipogenesis do not impair adipogenesis or triglyceride accumulation suggesting Ddx5 expression is dispensable in a mature adipocyte. Conclusion: These results implicate DDX5 as a crucial factor involved in the complex transcriptional cascade of events that regulate adipogenesis and essential to the initiation of adipogenesis. © 2015 Ramanathan et al. | Source Title: | Lipids in Health and Disease | URI: | https://scholarbank.nus.edu.sg/handle/10635/181415 | ISSN: | 1476511X | DOI: | 10.1186/s12944-015-0163-6 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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