Loss of ciliary transition zone protein TMEM107 leads to heterotaxy in mice

Dev Biol. 2020 Apr 15;460(2):187-199. doi: 10.1016/j.ydbio.2019.12.014. Epub 2019 Dec 27.

Abstract

Cilia in most vertebrate left-right organizers are involved in the original break in left-right (L-R) symmetry, however, less is known about their roles in subsequent steps of the cascade - relaying the signaling and maintaining the established asymmetry. Here we describe the L-R patterning cascades in two mutants of a ciliary transition zone protein TMEM107, revealing that near-complete loss of cilia in Tmem107null leads to left pulmonary isomerism due to the failure of the midline barrier. Contrary, partially retained cilia in the node and the midline of a hypomorphic Tmem107schlei mutant appear sufficient for the formation of the midline barrier and establishment and maintenance of the L-R asymmetry. Despite misregulation of Shh signaling in both mutants, the presence of normal Lefty1 expression and midline barrier formation in Tmem107schlei mutants, suggests a requirement for cilia, but not necessarily Shh signaling for Lefty1 expression and midline barrier formation.

Keywords: Cilia; Left-right asymmetry; Midline barrier; Shh; TMEM107.

Publication types

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

MeSH terms

  • Animals
  • Cilia* / genetics
  • Cilia* / metabolism
  • Cilia* / pathology
  • Hedgehog Proteins / genetics
  • Hedgehog Proteins / metabolism
  • Heterotaxy Syndrome* / embryology
  • Heterotaxy Syndrome* / genetics
  • Heterotaxy Syndrome* / pathology
  • Lung* / embryology
  • Lung* / pathology
  • Membrane Proteins / deficiency*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Transgenic
  • Signal Transduction*

Substances

  • Hedgehog Proteins
  • Membrane Proteins
  • Shh protein, mouse
  • Tmem107 protein, mouse