mRNA localization is a common mode of posttranscriptional regulation of gene expression that targets a protein to its site of function.^[1] Proteins are highly dependent on cellular environments for stability and function, therefore, mRNA localization signals are crucial for maintaining protein function. The Gurken localisation signal is an RNA regulatory element conserved across many species of Drosophila. The element consists of an RNA stem loop within the coding region of the messenger RNA that forms a signal for dynein-mediated Gurken mRNA transport to the dorsoanterior cap near the nucleus of the oocyte.^[2]

During Drosophila oogenesis, signaling between the germline and the soma leads to the establishment of anterior-posterior polarity in the egg and the embryo. This process involves the interaction of gurken (grk), a TGFα-like protein, with torpedo (top), the Drosophila epidermal growth factor receptor (EGFR).^[3][4] Localization of gurken RNA defines cell morphology by regulating the distribution of the gurken protein.^[4] Gurken mRNA transcripts which are not localized to the dorsal-anterior of an oocyte become silenced via post-translational modifications.^[3] Post-translational modifications of gurken protein have been observed to determine the protein's localization and function. Polyadenylation of gurken transcripts occur throughout oogenesis; the length of the poly(A) tail determines the stage in oogenesis at which the gurken protein is adenylated.^[3] 30-50 gurken adenlyated residues are associated in initial oogenesis whilst 50-90 adenlyated residues are associated with late-stage oogenesis.

The major difference between the gurken localization signal and other localization signals is that gurken localization signals are distributed throughout coding regions, whereas the majority of the other localization signals are found in 3' untranslated regions.[9].^[4] The gurken localization signal does not function properly if it is located in the 3' untranslated region.^[4]