ZFIN ID: ZDB-PUB-161220-9
Methods for the analysis of early oogenesis in zebrafish
Elkouby, Y.M., Mullins, M.C.
Date: 2017
Source: Developmental Biology   430(2): 310-324 (Journal)
Registered Authors: Elkouby, Yaniv M., Mullins, Mary C.
Keywords: Balbiani body, Oocyte polarity, animal-vegetal axis, centrosome, chromosomal bouquet, immune-fluorescence, in situ hybridization, live time-lapse imaging, meiosis, oocyte isolation, oogenesis, ovarian culture, ovary development, quantitative image analysis, symmetry-breaking, zebrafish
MeSH Terms:
  • Animals
  • Cells, Cultured
  • Cytoskeleton/ultrastructure
  • DNA/analysis
  • Female
  • Genes, Reporter
  • In Situ Hybridization, Fluorescence/methods
  • Luminescent Proteins/analysis
  • Luminescent Proteins/genetics
  • Meiosis
  • Microscopy, Confocal/instrumentation
  • Microscopy, Confocal/methods
  • Oocytes/physiology
  • Oocytes/ultrastructure
  • Oogenesis*
  • Organelles/physiology
  • Organelles/ultrastructure
  • Ovary/cytology
  • Ovary/growth & development
  • Ovum/chemistry
  • Ovum/physiology*
  • Ovum/ultrastructure
  • RNA, Messenger/analysis
  • Sex Determination Processes
  • Specimen Handling/methods*
  • Staining and Labeling/methods
  • Time-Lapse Imaging/methods*
  • Zebrafish
PubMed: 27988227 Full text @ Dev. Biol.
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ABSTRACT
Oocyte differentiation is a highly dynamic and intricate developmental process whose mechanistic understanding advances female reproduction, fertility, and ovarian cancer biology. Despite the many attributes of the zebrafish model, it has yet to be fully exploited for the investigation of early oocyte differentiation and ovarian development. This is partly because the properties of the adult zebrafish ovary make it technically challenging to access early stage oocytes. As a result, characterization of these stages has been lacking and tools for their analysis have been insufficient. To overcome these technical hurdles, we took advantage of the juvenile zebrafish ovary, where early stage oocytes can readily be found in high numbers and progress in a predictable manner. We characterized the earliest stages of oocyte differentiation and ovarian development and defined accurate staging criteria. We further developed protocols for quantitative microscopy, live time-lapse imaging, ovarian culture, and isolation of stage-specific oocytes for biochemical analysis. These methods have recently provided us with an unprecedented view of early oogenesis, allowing us to study formation of the Balbiani body, a universal oocyte granule that is associated with oocyte survival in mice and required for oocyte and egg polarity in fish and frogs. Despite its tremendous developmental significance, the Bb has been little investigated and how it forms was unknown in any species for over two centuries. We were able to trace Balbiani body formation and oocyte symmetry breaking to the onset of meiosis. Through this investigation we revealed novel cytoskeletal structures in oocytes and the contribution of specialized cellular organization to differentiation. Overall, the juvenile zebrafish ovary arises as an exciting model for studies of cell and developmental biology. We review these and other recent advances in vertebrate oogenesis in an accompanying manuscript in this issue of Developmental Biology. Here, we describe the protocols for ovarian investigation that we developed in the zebrafish, including all experimental steps that will easily allow others to reproduce such analysis. This juvenile ovary toolbox also contributes to establishing the zebrafish as a model for post-larval developmental stages.
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