@article{83971,
  keywords = {Animals, RNA, Messenger, Recombinant Fusion Proteins, Female, Gene Expression Regulation, Developmental, Body Patterning, Embryo, Nonmammalian, Oocytes, Drosophila melanogaster, Staining and Labeling, Fixatives, In Situ Hybridization, Fluorescence, Single Molecule Imaging, Tissue Fixation},
  author = {Evan Abbaszadeh and Elizabeth Gavis},
  title = {Fixed and live visualization of RNAs in Drosophila oocytes and embryos.},
  abstract = {<p>The ability to visualize RNA in situ is essential to dissect mechanisms for the temporal and spatial regulation of gene expression that drives development. Although considerable attention has been focused on transcriptional control, studies in model organisms like Drosophila have highlighted the importance of post-transcriptional mechanisms - most notably intracellular mRNA localization - in the formation and patterning of the body axes, specification of cell fates, and polarized cell functions. Our understanding of both types of regulation has been greatly advanced by technological innovations that enable a combination of highly quantitative and dynamic analysis of RNA. This review presents two methods, single molecule fluorescence in situ hybridization for high resolution quantitative RNA detection in fixed Drosophila oocytes and embryos and genetically encoded fluorescent RNA labeling for detection in live cells.</p>
},
  year = {2016},
  journal = {Methods},
  volume = {98},
  pages = {34-41},
  month = {04/2016},
  issn = {1095-9130},
  doi = {10.1016/j.ymeth.2016.01.018},
  language = {eng},
}