Transgenic RNAi in mouse oocytes: the first decade.

Anim Reprod Sci

Institute of Molecular Genetics AS CR, Videnska 1083, Prague, Czech Republic.

Published: September 2012

AI Article Synopsis

  • RNA interference (RNAi) is a method used to specifically silence genes through the degradation of mRNA using double-stranded RNA (dsRNA), with long dsRNA commonly used in plants and invertebrates.
  • In mammals, short RNA molecules are preferred to avoid an immune response triggered by long dsRNA, although mammalian oocytes can effectively use long dsRNA for RNAi without this response.
  • The paper reviews the development of a vector for oocyte-specific expression of dsRNA, detailing the advantages and challenges faced by researchers utilizing this transgenic RNAi system in studying gene function in mouse oocytes.

Article Abstract

RNA interference (RNAi), a sequence-specific mRNA degradation induced by double-stranded RNA (dsRNA), is a common approach employed to specifically silence genes. Experimental RNAi in plant and invertebrate models is frequently induced by long dsRNA. However, in mammals, short RNA molecules are used preferentially since long dsRNA can provoke sequence-independent type I interferon response. A notable exception are mammalian oocytes where the interferon response is suppressed and long dsRNA is a potent and specific trigger of RNAi. Transgenic RNAi is an adaptation of RNAi allowing for inducing sequence-specific silencing upon expression of dsRNA. A decade ago, we have developed a vector for oocyte-specific expression of dsRNA, which has been used to study gene function in mouse oocytes on numerous occasions. This review provides an overview and discusses benefits and drawbacks encountered by us and our colleagues while working with the oocytes-specific transgenic RNAi system.

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Source
http://dx.doi.org/10.1016/j.anireprosci.2012.08.012DOI Listing

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