Gonsalvez GB , Long RM .

	Figure 1. A general pathway for cytoplasmic RNA localization can be broken into distinct stepsStep 1 – RNA localization substrates (green line) can be identified in the nucleus by RNA-binding proteins (purple ball). Step 2 – the RNA-protein complex is exported from the nucleus to the cytoplasm through the nuclear pore complex. Step 3 – once in the cytoplasm, the RNA can associate with additional proteins (red) that interface the RNA with motor proteins (blue) that transport the RNA along cytoskeletal filaments (gray) to the site of localization. Step 4 – upon reaching the correct destination, translational repression is relieved and the corresponding protein (green ball) is synthesized at the site of action.
	Figure 2. ASH1 mRNA localization in S. cerevisiaeThe distribution of ASH1 mRNA is shown in red, and the positions of the nuclei are shown in blue.
	Figure 3. mRNA localization in Drosophila oocytesA schematic representation of the Drosophila egg chamber (top panel) oskar mRNA is transcribed in the nurse cells, transported into the oocyte and localized at the posterior pole (red). The bottom panel shows oskar mRNA (red) localization as detected by in situ hybridization. DAPI stained DNA is shown in blue.

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