Our final high-ranking candidate in Qrr1d is Fmn2. It codes for an actin binding protein exclusively expressed in the CNS and oocytes, and is involved in the establishment of cell polarity [70],[71]. In Drosophila, the formin homolog, cappuccino, has a role in RNA transport and in localizing the staufen protein to oocyte poles [100]–[102]. It is possible that FMN2 has parallel functions in mammalian neurons. Interestingly, Staufen 2 (Stau2), a gene involved in RNA transport to dendrites [62], maps to Qrr1d in BXD CNS datasets. Furthermore, deletion of formin homologs in yeast results in inhibition of protein translation [103], compelling evidence for an interaction between the protein translation system and formins. Evidence for a role for Fmn2 in dendrites also comes from our immunocytochemical analysis that clearly demonstrates the expression of FMN2 protein in dendrites. Taken together, Fmn2 is a functionally relevant candidate gene in Qrr1d and may be related to RNA transport and protein synthesis in the CNS.
