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Updated: May 2, 2026

Visualizing and Tracking Endogenous mRNAs in Live Drosophila melanogaster Egg Chambers
Published on: June 4, 2019
A stem-loop structure directs oskar mRNA to microtubule minus ends
Abstract:
mRNA transport coupled with translational control underlies the intracellular localization of many proteins in eukaryotic cells. This is exemplified in Drosophila, where oskar mRNA transport and translation at the posterior pole of the oocyte direct posterior patterning of the embryo. oskar localization is a multistep process. Within the oocyte, a spliced oskar localization element (SOLE) targets oskar mRNA for plus end-directed transport by kinesin-1 to the posterior pole. However, the signals mediating the initial minus end-directed, dynein-dependent transport of the mRNA from nurse cells into the oocyte have remained unknown. Here, we show that a 67-nt stem-loop in the oskar 3' UTR promotes oskar mRNA delivery to the developing oocyte and that it shares functional features with the fs(1)K10 oocyte localization signal. Thus, two independent cis-acting signals, the oocyte entry signal (OES) and the SOLE, mediate sequential dynein- and kinesin-dependent phases of oskar mRNA transport during oogenesis. The OES also promotes apical localization of injected RNAs in blastoderm stage embryos, another dynein-mediated process. Similarly, when ectopically expressed in polarized cells of the follicular epithelium or salivary glands, reporter RNAs bearing the oskar OES are apically enriched, demonstrating that this element promotes mRNA localization independently of cell type. Our work sheds new light on how oskar mRNA is trafficked during oogenesis and the RNA features that mediate minus end-directed transport.
Insights
Researchers identified a novel RNA element, the oocyte entry signal (OES), crucial for transporting oskar mRNA into the Drosophila oocyte. This discovery clarifies the initial dynein-dependent phase of mRNA trafficking during oogenesis.
Area of Science:
- Developmental Biology
- Molecular Cell Biology
- Genetics
Background:
- Intracellular mRNA transport and translational control are vital for protein localization in eukaryotes.
- In Drosophila, oskar mRNA localization to the oocyte posterior directs embryonic patterning.
- Previous studies identified the spliced oskar localization element (SOLE) for kinesin-1 mediated transport within the oocyte.
Purpose of the Study:
- To identify the signals responsible for the initial minus end-directed, dynein-dependent transport of oskar mRNA from nurse cells into the oocyte.
- To elucidate the RNA features mediating this early phase of mRNA transport during oogenesis.
Main Methods:
- Identification and functional analysis of a 67-nt stem-loop in the oskar 3' UTR.
- Assays for mRNA delivery to the developing oocyte and localization in blastoderm stage embryos.
- Ectopic expression studies in polarized follicular epithelium and salivary gland cells.
Main Results:
- A 67-nucleotide stem-loop in the oskar 3' UTR, termed the oocyte entry signal (OES), promotes oskar mRNA delivery into the oocyte.
- The OES mediates dynein-dependent transport and shares features with the fs(1)K10 oocyte localization signal.
- The OES drives apical localization of reporter RNAs in various cell types and embryonic stages, independent of cell type.
Conclusions:
- Two distinct cis-acting signals, OES and SOLE, mediate sequential dynein- and kinesin-dependent transport phases of oskar mRNA during oogenesis.
- The OES is a key determinant for the initial, minus end-directed transport of oskar mRNA into the oocyte.
- The OES promotes mRNA localization via dynein-dependent mechanisms, applicable across different cell types and developmental stages.
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