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Modifier variant of METTL13 suppresses human GAB1–associated profound deafness
Rizwan Yousaf, … , Thomas B. Friedman, Saima Riazuddin
Rizwan Yousaf, … , Thomas B. Friedman, Saima Riazuddin
Published February 6, 2018
Citation Information: J Clin Invest. 2018;128(4):1509-1522. https://doi.org/10.1172/JCI97350.
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Research Article Genetics Otology

Modifier variant of METTL13 suppresses human GAB1–associated profound deafness

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Abstract

A modifier variant can abrogate the risk of a monogenic disorder. DFNM1 is a locus on chromosome 1 encoding a dominant suppressor of human DFNB26 recessive, profound deafness. Here, we report that DFNB26 is associated with a substitution (p.Gly116Glu) in the pleckstrin homology domain of GRB2-associated binding protein 1 (GAB1), an essential scaffold in the MET proto-oncogene, receptor tyrosine kinase/HGF (MET/HGF) pathway. A dominant substitution (p.Arg544Gln) of METTL13, encoding a predicted methyltransferase, is the DFNM1 suppressor of GAB1-associated deafness. In zebrafish, human METTL13 mRNA harboring the modifier allele rescued the GAB1-associated morphant phenotype. In mice, GAB1 and METTL13 colocalized in auditory sensory neurons, and METTL13 coimmunoprecipitated with GAB1 and SPRY2, indicating at least a tripartite complex. Expression of MET-signaling genes in human lymphoblastoid cells of individuals homozygous for p.Gly116Glu GAB1 revealed dysregulation of HGF, MET, SHP2, and SPRY2, all of which have reported variants associated with deafness. However, SPRY2 was not dysregulated in normal-hearing humans homozygous for both the GAB1 DFNB26 deafness variant and the dominant METTL13 deafness suppressor, indicating a plausible mechanism of suppression. Identification of METTL13-based modification of MET signaling offers a potential therapeutic strategy for a wide range of associated hearing disorders. Furthermore, MET signaling is essential for diverse functions in many tissues including the inner ear. Therefore, identification of the modifier of MET signaling is likely to have broad clinical implications.

Authors

Rizwan Yousaf, Zubair M. Ahmed, Arnaud P.J. Giese, Robert J. Morell, Ayala Lagziel, Alain Dabdoub, Edward R. Wilcox, Sheikh Riazuddin, Thomas B. Friedman, Saima Riazuddin

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Figure 7

METTL13 interacts with GAB1 and SPROUTY2.

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METTL13 interacts with GAB1 and SPROUTY2.
(A) Lysates from HEK293 cells ...
(A) Lysates from HEK293 cells transfected with both normal and mutant METTL13-Flag– along with normal and mutant GAB1-HA– and Myc-tagged SPRY2 expression constructs in various combinations were used for co-IP assays with anti-Flag antibody–coated beads. Precipitates were immunoblotted with antibodies against Flag, HA, and Myc tags. (B) Co-IP assay shows an absence of interaction between GAB1WT-GFP and SPRY2WT-Myc.
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