4.7 Article

Pitx2c ensures habenular asymmetry by restricting parapineal cell number

Journal

DEVELOPMENT
Volume 141, Issue 7, Pages 1572-1579

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.100305

Keywords

Nodal; Pitx2; Epithalamus; Left-right; Parapineal; Zebrafish

Funding

  1. Centre national de la recherche scientifique (CNRS)
  2. Institut national de la sante et de la recherche medicale (INSERM)
  3. Universite de Toulouse III (UPS)
  4. Fondation l'Association pour la recherche sur le cancer (ARC) [SFI20101201699]
  5. French Ministere de la Recherche
  6. National Institutes of Health/National Institute of Child Health and Human Development (NIH/NICHD) [HD054534]

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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.

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