Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes
- PMID: 37830236
- PMCID: PMC11014897
- DOI: 10.1002/jez.b.23222
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes
Abstract
Hearing in infants is essential for brain development, acquisition of verbal language skills, and development of social interactions. Therefore, it is important to diagnose hearing loss soon after birth so that interventions can be provided as early as possible. Most newborns in the United States are screened for hearing deficits and commercially available next-generation sequencing hearing loss panels often can identify the causative gene, which may also identify congenital defects in other organs. One of the most prevalent autosomal dominant congenital hearing loss syndromes is branchio-oto-renal syndrome (BOR), which also presents with defects in craniofacial structures and the kidney. Currently, mutations in three genes, SIX1, SIX5, and EYA1, are known to be causative in about half of the BOR patients that have been tested. To uncover new candidate genes that could be added to congenital hearing loss genetic screens, we have combined the power of Drosophila mutants and protein biochemical assays with the embryological advantages of Xenopus, a key aquatic animal model with a high level of genomic similarity to human, to identify potential Six1 transcriptional targets and interacting proteins that play a role during otic development. We review our transcriptomic, yeast 2-hybrid, and proteomic approaches that have revealed a large number of new candidates. We also discuss how we have begun to identify how Six1 and co-factors interact to direct developmental events necessary for normal otic development.
Keywords: BOR; Eya1; Mcsr1; Pa2G4; Six1; Sobp; Zmym2; Zmym4.
© 2023 The Authors. Journal of Experimental Zoology Part B: Molecular and Developmental Evolution published by Wiley Periodicals LLC.
Conflict of interest statement
Similar articles
-
Using Xenopus to discover new genes involved in branchiootorenal spectrum disorders.Comp Biochem Physiol C Toxicol Pharmacol. 2015 Dec;178:16-24. doi: 10.1016/j.cbpc.2015.06.007. Epub 2015 Jun 24. Comp Biochem Physiol C Toxicol Pharmacol. 2015. PMID: 26117063 Free PMC article. Review.
-
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development.Development. 2021 Sep 1;148(17):dev199684. doi: 10.1242/dev.199684. Epub 2021 Sep 6. Development. 2021. PMID: 34414417 Free PMC article.
-
Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development.Dis Model Mech. 2020 Mar 3;13(3):dmm043489. doi: 10.1242/dmm.043489. Dis Model Mech. 2020. PMID: 31980437 Free PMC article.
-
EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis.Biol Cell. 2010 Feb 17;102(5):277-92. doi: 10.1042/BC20090098. Biol Cell. 2010. PMID: 19951260 Free PMC article.
-
Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan.Pediatr Int. 2014 Jun;56(3):309-14. doi: 10.1111/ped.12357. Pediatr Int. 2014. PMID: 24730701 Review.
Cited by
-
Bop1 is required to establish precursor domains of craniofacial tissues.Genesis. 2024 Feb;62(1):e23580. doi: 10.1002/dvg.23580. Epub 2023 Nov 16. Genesis. 2024. PMID: 37974491 Free PMC article.
References
-
- Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Levi-Acobas F, Cruaud C, Le Merrer M, Mathieu M, Konig R, Vigneron J, Weissenbach J, Petit C, Weil D, 1997. Clustering of mutation responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous regions (eyaHR) of EYA1. Hum. Mol. Genet 6, 2247–2255. - PubMed
-
- Bajoghli B, Aghaallaei N, Czerby T, 2005. Groucho corepressor proteins regulate otic vesicle outgrowth. Dev. Dyn 233, 760–771. - PubMed
-
- Bane BC, Van Rybroek JM, Kolker SJ, Weeks DL, Manaligod JM, 2005. EYA1 expression in the developing inner ear. Ann. Otol. Rhinol. Laryngol 114, 853–858. - PubMed
-
- Bartel PL, Fields S, 1993. Analyzing protein-protein interactions using two-hybrid system. Methods in Enzymology 254, 241–263. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials