ZFIN ID: ZDB-PUB-191124-8
Left-right asymmetric heart jogging increases the robustness of dextral heart looping in zebrafish
Grimes, D.T., Patterson, V.L., Luna-Arvizu, G., Schottenfeld-Roames, J., Irons, Z.H., Burdine, R.D.
Date: 2019
Source: Developmental Biology   459(2): 79-86 (Journal)
Registered Authors: Burdine, Rebecca, Grimes, Daniel T.
Keywords: Chirality, Heart jogging, Heart looping, Heterotaxy, Left-right asymmetry, Morphogenesis, Nodal, Zebrafish
MeSH Terms:
  • Animals
  • Body Patterning/genetics*
  • Embryonic Development/genetics*
  • Female
  • Gene Expression Regulation, Developmental
  • Gene Knockdown Techniques
  • Heart/embryology*
  • Loss of Function Mutation
  • Male
  • Mesoderm/metabolism
  • Myocardium/metabolism
  • Nodal Protein/metabolism
  • Organogenesis/genetics*
  • Signal Transduction/genetics
  • Transforming Growth Factor beta2/genetics
  • Transforming Growth Factor beta2/metabolism
  • Zebrafish/embryology*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed: 31758943 Full text @ Dev. Biol.
Building a left-right (L-R) asymmetric organ requires asymmetric information. This comes from various sources, including asymmetries in embryo-scale genetic cascades, organ-intrinsic mechanical forces, and cell-level chirality, but the relative influence of these sources and how they collaborate to drive asymmetric morphogenesis is not understood. During zebrafish heart development, the linear heart tube extends to the left of the midline in a process known as jogging. The jogged heart then undergoes dextral (i.e. rightward) looping to correctly position the heart chambers relative to one another. Left lateralized jogging is governed by the left-sided expression of Nodal in mesoderm tissue, while looping laterality is mainly controlled by heart-intrinsic cell-level asymmetries in the actomyosin cytoskeleton. The purpose of lateralized jogging is not known. Moreover, after jogging, the heart tube returns to a midline position and so it is not clear whether or how jogging may impact the dextral loop. Here, we characterize a novel loss-of-function mutant in the zebrafish Nodal homolog southpaw (spaw) that appears to be a true null. We then assess the relationship between jogging and looping laterality in embryos lacking asymmetric Spaw signals. We found that the probability of a dextral loop occurring, as opposed to improper lateralization of looping, does not depend on asymmetric Spaw signals per se, but does depend on the laterality of jogging. Thus, we conclude that the role of leftward jogging is to spatially position the heart tube in a manner that promotes robust dextral looping. When jogging laterality is abnormal, the robustness of dextral looping decreases. This establishes a cooperation between embryo-scale Spaw-dependent L-R asymmetries and organ-intrinsic cellular chirality in the control of asymmetric heart morphogenesis and shows that the transient laterality of the early heart tube has consequences for later heart morphogenetic events.