Pitx2c ensures habenular asymmetry by restricting parapineal cell number

Garric, L., Ronsin, B., Roussigné, M., Booton, S., Gamse, J.T., Dufourcq, P., Blader, P.
Development (Cambridge, England)   141: 1572-9 (Journal)
Registered Authors
Blader, Patrick, Dufourcq, Pascale, Gamse, Josh, Roussigné, Myriam
Epithalamus, Left-right, Nodal, Parapineal, Pitx2, Zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Body Patterning/genetics*
  • Cell Count
  • Embryo, Nonmammalian
  • Epithalamus/cytology
  • Epithalamus/embryology
  • Habenula/cytology
  • Habenula/embryology*
  • Nodal Protein/physiology
  • Organ Size/genetics
  • Pineal Gland/cytology
  • Pineal Gland/embryology*
  • Signal Transduction/physiology
  • Transcription Factors/genetics
  • Transcription Factors/physiology*
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/physiology*
24598158 Full text @ Development
Left-right (L/R) asymmetries in the brain are thought to underlie lateralised cognitive functions. Understanding how neuroanatomical asymmetries are established has been achieved through the study of the zebrafish epithalamus. Morphological symmetry in the epithalamus is broken by leftward migration of the parapineal, which is required for the subsequent elaboration of left habenular identity; the habenular nuclei flank the midline and show L/R asymmetries in marker expression and connectivity. The Nodal target pitx2c is expressed in the left epithalamus, but nothing is known about its role during the establishment of asymmetry in the brain. We show that abrogating Pitx2c function leads to the right habenula adopting aspects of left character, and to an increase in parapineal cell numbers. Parapineal ablation in Pitx2c loss of function results in right habenular isomerism, indicating that the parapineal is required for the left character detected in the right habenula in this context. Partial parapineal ablation in the absence of Pitx2c, however, reduces the number of parapineal cells to wild-type levels and restores habenular asymmetry. We provide evidence suggesting that antagonism between Nodal and Pitx2c activities sets an upper limit on parapineal cell numbers. We conclude that restricting parapineal cell number is crucial for the correct elaboration of epithalamic asymmetry.
Genes / Markers
Figure Gallery
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Engineered Foreign Genes
Errata and Notes