Asymmetric cell convergence-driven zebrafish fin bud initiation and pre-pattern requires Tbx5a control of a mesenchymal Fgf signal

Development. 2015 Dec 15;142(24):4329-39. doi: 10.1242/dev.124750. Epub 2015 Nov 2.

Abstract

Tbx5 plays a pivotal role in vertebrate forelimb initiation, and loss-of-function experiments result in deformed or absent forelimbs in all taxa studied to date. Combining single-cell fate mapping and three-dimensional cell tracking in the zebrafish, we describe a Tbx5a-dependent cell convergence pattern that is both asymmetric and topological within the fin-field lateral plate mesoderm during early fin bud initiation. We further demonstrate that a mesodermal Fgf24 convergence cue controlled by Tbx5a underlies this asymmetric convergent motility. Partial reduction in Tbx5a or Fgf24 levels disrupts the normal fin-field cell motility gradient and results in anteriorly biased perturbations of fin-field cell convergence and truncations in the pectoral fin skeleton, resembling aspects of the forelimb skeletal defects that define individuals with Holt-Oram syndrome. This study provides a quantitative reference model for fin-field cell motility during vertebrate fin bud initiation and suggests that a pre-pattern of anteroposterior fate specification is already present in the fin-field before or during migration because perturbations to these early cell movements result in the alteration of specific fates.

Keywords: Cell migration; Chemoattractant; Fgf24; Holt–Oram syndrome; Lateral plate mesoderm; Limb bud (fin bud); Limb-field (fin-field); Tbx5a; Zebrafish.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animal Fins / cytology*
  • Animal Fins / embryology*
  • Animals
  • Body Patterning*
  • Cell Movement
  • Cell Tracking
  • Embryo, Nonmammalian / metabolism
  • Fibroblast Growth Factors / metabolism*
  • Gene Expression Regulation, Developmental
  • Mesoderm / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Signal Transduction* / genetics
  • Single-Cell Analysis
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism*
  • Time-Lapse Imaging
  • Zebrafish / embryology*
  • Zebrafish / genetics
  • Zebrafish Proteins / metabolism*

Substances

  • RNA, Messenger
  • T-Box Domain Proteins
  • T-box transcription factor 5
  • Zebrafish Proteins
  • fgf8a protein, zebrafish
  • fibroblast growth factor 24, zebrafish
  • Fibroblast Growth Factors