OTX2 mutations contribute to the otocephaly-dysgnathia complex

Nicolas Chassaing, Susanna Sorrentino, Erica E. Davis, Dominique Martin-Coignard, Anthony Iacovelli, William Paznekas, Bryn D. Webb, Ona Faye-Petersen, Férechté Encha-Razavi, Leopoldine Lequeux, Adeline Vigouroux, Ahmet Yesilyurt, Simeon A. Boyadjiev, Hülya Kayserili, Philippe Loget, Dominique Carles, Consolato Sergi, Surasak Puvabanditsin, Chih Ping Chen, Heather C. Etchevers & 4 others Nicholas Katsanis, Catherine L. Mercer, Patrick Calvas, Ethylin Wang Jabs

Research output: Contribution to journalArticle

Abstract

Background Otocephaly or dysgnathia complex is characterised by mandibular hypoplasia/agenesis, ear anomalies, microstomia, and microglossia; the molecular basis of this developmental defect is largely unknown in humans. Methods and results This study reports a large family in which two cousins with micro/anophthalmia each gave birth to at least one child with otocephaly, suggesting a genetic relationship between anophthalmia and otocephaly. OTX2, a known microphthalmia locus, was screened in this family and a frameshifting mutation was found. The study subsequently identified in one unrelated otocephalic patient a sporadic OTX2 mutation. Because OTX2 mutations may not be sufficient to cause otocephaly, the study assayed the potential of otx2 to modify craniofacial phenotypes in the context of known otocephaly gene suppression in vivo. It was found that otx2 can interact genetically with pgap1, prrx1, and msx1 to exacerbate mandibular and midline defects during zebrafish development. However, sequencing of these loci in the OTX2-positive families did not unearth likely pathogenic lesions, suggesting further genetic heterogeneity and complexity. Conclusion Identification of OTX2 involvement in otocephaly/dysgnathia in humans, even if loss of function mutations at this locus does not sufficiently explain the complex anatomical defects of these patients, suggests the requirement for a second genetic hit. Consistent with this notion, trans suppression of otx2 and other developmentally related genes recapitulate aspects of the otocephaly phenotype in zebrafish. This study highlights the combined utility of genetics and functional approaches to dissect both the regulatory pathways that govern craniofacial development and the genetics of this disease group.

Original languageEnglish (US)
Pages (from-to)373-379
Number of pages7
JournalJournal of Medical Genetics
Volume49
Issue number6
DOIs
StatePublished - Jun 2012
Externally publishedYes

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Mutation
Anophthalmos
Zebrafish
Tongue Diseases
Microstomia
Microphthalmos
Phenotype
Inborn Genetic Diseases
Genetic Heterogeneity
Otocephaly
Dysgnathia complex
Genes
Ear
Parturition

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Chassaing, N., Sorrentino, S., Davis, E. E., Martin-Coignard, D., Iacovelli, A., Paznekas, W., ... Jabs, E. W. (2012). OTX2 mutations contribute to the otocephaly-dysgnathia complex. Journal of Medical Genetics, 49(6), 373-379. https://doi.org/10.1136/jmedgenet-2012-100892

OTX2 mutations contribute to the otocephaly-dysgnathia complex. / Chassaing, Nicolas; Sorrentino, Susanna; Davis, Erica E.; Martin-Coignard, Dominique; Iacovelli, Anthony; Paznekas, William; Webb, Bryn D.; Faye-Petersen, Ona; Encha-Razavi, Férechté; Lequeux, Leopoldine; Vigouroux, Adeline; Yesilyurt, Ahmet; Boyadjiev, Simeon A.; Kayserili, Hülya; Loget, Philippe; Carles, Dominique; Sergi, Consolato; Puvabanditsin, Surasak; Chen, Chih Ping; Etchevers, Heather C.; Katsanis, Nicholas; Mercer, Catherine L.; Calvas, Patrick; Jabs, Ethylin Wang.

In: Journal of Medical Genetics, Vol. 49, No. 6, 06.2012, p. 373-379.

Research output: Contribution to journalArticle

Chassaing, N, Sorrentino, S, Davis, EE, Martin-Coignard, D, Iacovelli, A, Paznekas, W, Webb, BD, Faye-Petersen, O, Encha-Razavi, F, Lequeux, L, Vigouroux, A, Yesilyurt, A, Boyadjiev, SA, Kayserili, H, Loget, P, Carles, D, Sergi, C, Puvabanditsin, S, Chen, CP, Etchevers, HC, Katsanis, N, Mercer, CL, Calvas, P & Jabs, EW 2012, 'OTX2 mutations contribute to the otocephaly-dysgnathia complex', Journal of Medical Genetics, vol. 49, no. 6, pp. 373-379. https://doi.org/10.1136/jmedgenet-2012-100892
Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W et al. OTX2 mutations contribute to the otocephaly-dysgnathia complex. Journal of Medical Genetics. 2012 Jun;49(6):373-379. https://doi.org/10.1136/jmedgenet-2012-100892
Chassaing, Nicolas ; Sorrentino, Susanna ; Davis, Erica E. ; Martin-Coignard, Dominique ; Iacovelli, Anthony ; Paznekas, William ; Webb, Bryn D. ; Faye-Petersen, Ona ; Encha-Razavi, Férechté ; Lequeux, Leopoldine ; Vigouroux, Adeline ; Yesilyurt, Ahmet ; Boyadjiev, Simeon A. ; Kayserili, Hülya ; Loget, Philippe ; Carles, Dominique ; Sergi, Consolato ; Puvabanditsin, Surasak ; Chen, Chih Ping ; Etchevers, Heather C. ; Katsanis, Nicholas ; Mercer, Catherine L. ; Calvas, Patrick ; Jabs, Ethylin Wang. / OTX2 mutations contribute to the otocephaly-dysgnathia complex. In: Journal of Medical Genetics. 2012 ; Vol. 49, No. 6. pp. 373-379.
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abstract = "Background Otocephaly or dysgnathia complex is characterised by mandibular hypoplasia/agenesis, ear anomalies, microstomia, and microglossia; the molecular basis of this developmental defect is largely unknown in humans. Methods and results This study reports a large family in which two cousins with micro/anophthalmia each gave birth to at least one child with otocephaly, suggesting a genetic relationship between anophthalmia and otocephaly. OTX2, a known microphthalmia locus, was screened in this family and a frameshifting mutation was found. The study subsequently identified in one unrelated otocephalic patient a sporadic OTX2 mutation. Because OTX2 mutations may not be sufficient to cause otocephaly, the study assayed the potential of otx2 to modify craniofacial phenotypes in the context of known otocephaly gene suppression in vivo. It was found that otx2 can interact genetically with pgap1, prrx1, and msx1 to exacerbate mandibular and midline defects during zebrafish development. However, sequencing of these loci in the OTX2-positive families did not unearth likely pathogenic lesions, suggesting further genetic heterogeneity and complexity. Conclusion Identification of OTX2 involvement in otocephaly/dysgnathia in humans, even if loss of function mutations at this locus does not sufficiently explain the complex anatomical defects of these patients, suggests the requirement for a second genetic hit. Consistent with this notion, trans suppression of otx2 and other developmentally related genes recapitulate aspects of the otocephaly phenotype in zebrafish. This study highlights the combined utility of genetics and functional approaches to dissect both the regulatory pathways that govern craniofacial development and the genetics of this disease group.",
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T1 - OTX2 mutations contribute to the otocephaly-dysgnathia complex

AU - Chassaing, Nicolas

AU - Sorrentino, Susanna

AU - Davis, Erica E.

AU - Martin-Coignard, Dominique

AU - Iacovelli, Anthony

AU - Paznekas, William

AU - Webb, Bryn D.

AU - Faye-Petersen, Ona

AU - Encha-Razavi, Férechté

AU - Lequeux, Leopoldine

AU - Vigouroux, Adeline

AU - Yesilyurt, Ahmet

AU - Boyadjiev, Simeon A.

AU - Kayserili, Hülya

AU - Loget, Philippe

AU - Carles, Dominique

AU - Sergi, Consolato

AU - Puvabanditsin, Surasak

AU - Chen, Chih Ping

AU - Etchevers, Heather C.

AU - Katsanis, Nicholas

AU - Mercer, Catherine L.

AU - Calvas, Patrick

AU - Jabs, Ethylin Wang

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N2 - Background Otocephaly or dysgnathia complex is characterised by mandibular hypoplasia/agenesis, ear anomalies, microstomia, and microglossia; the molecular basis of this developmental defect is largely unknown in humans. Methods and results This study reports a large family in which two cousins with micro/anophthalmia each gave birth to at least one child with otocephaly, suggesting a genetic relationship between anophthalmia and otocephaly. OTX2, a known microphthalmia locus, was screened in this family and a frameshifting mutation was found. The study subsequently identified in one unrelated otocephalic patient a sporadic OTX2 mutation. Because OTX2 mutations may not be sufficient to cause otocephaly, the study assayed the potential of otx2 to modify craniofacial phenotypes in the context of known otocephaly gene suppression in vivo. It was found that otx2 can interact genetically with pgap1, prrx1, and msx1 to exacerbate mandibular and midline defects during zebrafish development. However, sequencing of these loci in the OTX2-positive families did not unearth likely pathogenic lesions, suggesting further genetic heterogeneity and complexity. Conclusion Identification of OTX2 involvement in otocephaly/dysgnathia in humans, even if loss of function mutations at this locus does not sufficiently explain the complex anatomical defects of these patients, suggests the requirement for a second genetic hit. Consistent with this notion, trans suppression of otx2 and other developmentally related genes recapitulate aspects of the otocephaly phenotype in zebrafish. This study highlights the combined utility of genetics and functional approaches to dissect both the regulatory pathways that govern craniofacial development and the genetics of this disease group.

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