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. 2018 Aug 28;19:634. doi: 10.1186/s12864-018-5020-3

Fig. 5.

Fig. 5

Quantification and analysis of the mito-piR-7,456,245 derived from mitochondria in 3T3-L1 cells. a Expression of 7 selected piRNAs in NGS libraries. The heat map colors correspond to log2 of the normalized read counts. b The RT-qPCR expression of 7 selected piRNAs in arbitrary units calculated using U6 derived piRNA as an endogenous standard. c Confocal images of cultured 3T3-L1 cells transfected with AntipiRNA-F fluorescent GapmeR, and stained with MitoTracker (mitochondria) and DAPI (nucleus). d Merged image of 3T3-L1 cells transfected with AntipiRNA-F fluorescent GapmeR, and stained with MitoTracker and DAPI. The arrows indicate the partial localization of the AntipiRNA-F fluorescent GapmeR and the mitochondria. Male cells: primordial germ cells (PGCs), spermatogonia cells (SPG), and spermatozoa (SPZ); female cells: oocytes (OCY); and zygotes (ZYGO). Bars represent 75 μm