Grk5l controls heart development by limiting mTOR signaling during symmetry breaking.


Journal Article

The correct asymmetric placement of inner organs is termed situs solitus and is determined early during development. Failure in symmetry breaking results in conditions ranging from randomized organ arrangement to a complete mirror image, often accompanied by severe congenital heart defects (CHDs). We found that the zebrafish homolog of mammalian G protein-coupled receptor kinase 5 (GRK5) employs noncanonical, receptor-independent functions to secure symmetry breaking. Knockdown of GRK5's closest homolog in zebrafish embryos, Grk5l, is sufficient to randomize cardiac looping and left-right asymmetry. Mechanistically, we found that loss of GRK5 increases mammalian target of rapamycin complex 1 (mTORC1) activity. This causes elongation of motile cilia in the organ of laterality, a consequence that is known to be sufficient to trigger aberrant organ arrangement. By fine-tuning mTORC1, GRK5 thus serves an unanticipated function during early development, besides its well-characterized role in the adult heart. These findings could implicate GRK5 as a susceptibility allele for certain cases of CHD.

Full Text

Duke Authors

Cited Authors

  • Burkhalter, MD; Fralish, GB; Premont, RT; Caron, MG; Philipp, M

Published Date

  • August 29, 2013

Published In

Volume / Issue

  • 4 / 4

Start / End Page

  • 625 - 632

PubMed ID

  • 23972986

Pubmed Central ID

  • 23972986

Electronic International Standard Serial Number (EISSN)

  • 2211-1247

Digital Object Identifier (DOI)

  • 10.1016/j.celrep.2013.07.036


  • eng

Conference Location

  • United States