Adapted Resistance to the Knockdown Effect of shRNA-Derived Srsf3 siRNAs in Mouse Littermates

Int J Biol Sci. 2015 Sep 3;11(11):1248-56. doi: 10.7150/ijbs.13011. eCollection 2015.

Abstract

Gene silencing techniques are widely used to control gene expression and have potential for RNAi-based therapeutics. In this report, transgenic mouse lines were created for conditional knockdown of Srsf3 (SRp20) expression in liver and mammary gland tissues by expressing Srsf3-specific shRNAs driven by a U6 promoter. Although a small portion of the transgenic mouse littermates were found to produce siRNAs in the targeted tissues, most of the transgenic littermates at two months of age failed to display a knockdown phenotype of Srsf3 expression in their liver and mammary gland tissues where an abundant level of Srsf3 siRNAs remained. We saw only one of four mice with liver/mammary gland expressing Srsf3 siRNA displayed a suppressed level of Srsf3 protein, but not the mRNA. Data indicate that the host resistance to a gene-specific siRNA targeting an essential gene transcript can be developed in animals, presumably as a physiological necessity to cope with the hostile perturbation.

Keywords: Srsf3; shRNAs; transgenic mouse.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Proliferation / physiology
  • Female
  • Gene Silencing / physiology
  • Liver / metabolism
  • Mammary Glands, Animal / metabolism
  • Mice
  • Mice, Transgenic
  • RNA Interference
  • RNA, Small Interfering / genetics
  • RNA-Binding Proteins / genetics*
  • RNA-Binding Proteins / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Serine-Arginine Splicing Factors

Substances

  • RNA, Small Interfering
  • RNA-Binding Proteins
  • Srsf3 protein, mouse
  • Serine-Arginine Splicing Factors