A two-cilia model for vertebrate left-right axis specification

CJ Tabin, KJ Vogan - Genes & development, 2003 - genesdev.cshlp.org
CJ Tabin, KJ Vogan
Genes & development, 2003genesdev.cshlp.org
The mechanisms underlying vertebrate left-right (LR) axis specification have attracted much
interest among developmental biologists (for review, see Burdine and Schier 2000;
Capdevila et al. 2000). Of particular interest from a conceptual standpoint is the question of
how LR positional information first originates within the context of a bilaterally symmetric
embryo. To achieve the consistent LR handedness characteristic of the vertebrate body
plan, the LR axis must be reliably oriented with respect to the other two embryonic axes …
The mechanisms underlying vertebrate left-right (LR) axis specification have attracted much interest among developmental biologists (for review, see Burdine and Schier 2000; Capdevila et al. 2000). Of particular interest from a conceptual standpoint is the question of how LR positional information first originates within the context of a bilaterally symmetric embryo. To achieve the consistent LR handedness characteristic of the vertebrate body plan, the LR axis must be reliably oriented with respect to the other two embryonic axes, anteroposterior (AP) and dorsoventral (DV; Brown and Wolpert 1990). Understanding how embryos achieve this goal without reference to any external cues represents a formidable challenge for embryologists and theoretical biologists alike.
The first breakthrough in understanding the molecular basis of handed asymmetry was the discovery of a cascade of signals produced asymmetrically in the early embryo that was sufficient to direct the orientation of later LR morphogenetic events (Levin et al. 1995). This, together with subsequent reports identifying additional genes expressed asymmetrically in the early embryo, opened the door to ongoing work directed at understanding how LR positional information is propagated in the embryo as well as how this information is ultimately translated into morphological manifestations of LR asymmetry (for review, see Burdine and Schier 2000; Capdevila et al. 2000). Perhaps most important, however, were the general patterns of asymmetric gene expression first reported by Levin et al.(1995)—initial tightly localized domains of asymmetric gene expression at the chick node (ActRIIa, Shh, and then Nodal medially) followed by broad domains of asymmetric gene expression throughout the lateral plate (Nodal in the left lateral plate mesoderm). Significantly, although some of the specific molecular players appear to vary across different species, the node has consistently been the location where the earliest molecular asymmetries are centered, drawing attention to this region as the most likely site for the initial symmetry breaking event responsible for specifying the orientation of the LR axis (Vogan and
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