PUBLICATION
A human laterality disorder caused by a homozygous deleterious mutation in MMP21
- Authors
- Perles, Z., Moon, S., Ta-Shma, A., Yaacov, B., Francescatto, L., Edvardson, S., Rein, A.J., Elpeleg, O., Katsanis, N.
- ID
- ZDB-PUB-151003-2
- Date
- 2015
- Source
- Journal of Medical Genetics 52(12): 840-7 (Journal)
- Registered Authors
- Francescatto, Ludmila, Katsanis, Nicholas
- Keywords
- Congenital heart disease, Developmental, Genetics
- MeSH Terms
-
- Animals
- Base Sequence
- Child
- Consanguinity
- DNA Mutational Analysis
- Exome
- Female
- Heterotaxy Syndrome/enzymology
- Heterotaxy Syndrome/genetics*
- Homozygote
- Humans
- Male
- Matrix Metalloproteinases, Secreted/genetics*
- Pedigree
- Receptors, Notch/metabolism
- Sequence Deletion
- Signal Transduction
- Young Adult
- Zebrafish
- PubMed
- 26429889 Full text @ J. Med. Genet.
Citation
Perles, Z., Moon, S., Ta-Shma, A., Yaacov, B., Francescatto, L., Edvardson, S., Rein, A.J., Elpeleg, O., Katsanis, N. (2015) A human laterality disorder caused by a homozygous deleterious mutation in MMP21. Journal of Medical Genetics. 52(12):840-7.
Abstract
Background Laterality in the vertebrate embryo is determined by left-right asymmetric gene expression driven by the flow of extraembryonic fluid across the embryonic node. Defects in these processes cause heterotaxy, the abnormal formation and arrangement of visceral organs that can range from complete inversion of symmetry to the selective misarrangement of organs. However, our understanding of the genetic causality for laterality defects in human beings remains relatively limited.
Methods We performed whole exome sequencing in a consanguineous family with heterotaxia. To interrogate the pathogenic potential of the discovered variant, we used an in vivo system in which the potential of the candidate gene to induce L-R asymmetry was tested by transient suppression and CRISPR/Cas9-induced deletions. We also used in vitro assays to test a possible link between our exome-derived candidate and Notch signaling.
Results We identified a homozygous 2 bp deletion in MMP21, encoding matrix metalloproteinase-21, as the sole coding mutation that segregated with the phenotype. Transient suppression or CRISPR/Cas9-mediated deletion of mmp21 in zebrafish embryos induced cardiac looping defects, with concomitant disruption of laterality markers in the lateral plate mesoderm and disrupted notch signalling in vitro and in vivo.
Conclusions Our data implicate loss of MMP21 as a cause of heterotaxy in humans with concomitant defects in Notch signaling. In support of this finding, a homozygous missense mutation in MMP21 was identified previously in mice with N-Ethyl-N-Nitrosourea (ENU)-induced heterotaxy. Taken together, these observations suggest a role of matrix metalloproteinases in the establishment of asymmetric organ development, likely through the regulation of morphogenetic signals.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping