, 1996). The function of ddc in the cod egg is not known, and likewise, it is not known if ddc plays immune-relevant roles in early life stage fishes. Since female 2 in our study had the highest quality eggs by a large margin, and acy3 transcript expression was lowest in female 2 fertilized and unfertilized eggs, it may be a candidate biomarker for extremes in egg quality. To our knowledge, there is no published information on acy3 gene expression or function in fish, and our study is the first to identify acy3 as a maternal transcript. In mammals, ACY3 (synonym: AA3) deacetylates mercapturic acids and N-acetyl amino acids with

aromatic side chains, and mediates the toxicity of trichloroethylene (an industrial solvent and environmental pollutant) ( Hsieh et al., 2010 and Tsirulnikov selleck chemicals llc et al., 2012). In addition, mammalian ACY3 binds to hepatitis C virus (HCV) core protein and may be involved in HCV-associated disease ( Chen et al., 2009 and Tsirulnikov et al., 2012). Despite what is known regarding mammalian ACY3 function, the lack of information on vertebrate egg or embryonic acy3 gene

expression or function makes it difficult to speculate about its potential role in the Atlantic cod egg. Our studies show that cod kpna7 and hacd1 are maternal transcripts expressed at a range of levels in eggs from different females ( Figs. 3D,E and 4D,E). The expression and function of kpna7 in the mammalian egg and early embryo have been extensively studied. Mammalian KPNA7 belongs to a family of seven importin α subtypes (Karyopherins α1-α7) that are involved Ganetespib research buy in the translocation of proteins with nuclear localization signals (including transcription factors and chromatin remodeling factors) into the nucleus ( Wang et al., 2012). The nuclear importing system and nuclear proteins

in mammals play key roles in early embryonic events (e.g. nuclear reprogramming and zygotic gene activation) that are required for successful development ( Hu et al., 2010). In mammals, kpna7 has been shown to play important roles in early embryonic development ( Tejomurtula et al., 2009, Wang et al., 2012 and Hu et al., 2010). Dichloromethane dehalogenase Bovine kpna7 is highly expressed at the transcript and protein levels in mature oocytes and 2-cell embryos, with lower expression in blastocyst stage embryos ( Tejomurtula et al., 2009). Mouse kpna7 transcript expression is high in mature oocytes, zygotes, and 2-cell embryos, and decreases drastically in 4-cell and subsequent embryonic stages, whereas mouse KPNA7 protein is highly expressed in mature oocytes and zygotes and drastically decreases at the 2-cell stage ( Hu et al., 2010). Targeted knockdown of bovine kpna7 by RNA interference caused a significant decrease in the proportion of embryos that reached the 8-cell to 16-cell stage ( Tejomurtula et al., 2009).