Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate. (May 2018)
- Record Type:
- Journal Article
- Title:
- Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate. (May 2018)
- Main Title:
- Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate
- Authors:
- Gowans, Lord Jephthah Joojo
Oseni, Ganiyu
Mossey, Peter A.
Adeyemo, Wasiu Lanre
Eshete, Mekonen A.
Busch, Tamara D.
Donkor, Peter
Obiri-Yeboah, Solomon
Plange-Rhule, Gyikua
Oti, Alexander A.
Owais, Arwa
Olaitan, Peter B.
Aregbesola, Babatunde S.
Oginni, Fadekemi O.
Bello, Seidu A.
Audu, Rosemary
Onwuamah, Chika
Agbenorku, Pius
Ogunlewe, Mobolanle O.
Abdur-Rahman, Lukman O.
Marazita, Mary L.
Adeyemo, A. A.
Murray, Jeffrey C.
Butali, Azeez - Abstract:
- Objective: Cleft lip and/or cleft palate (CL/P) are congenital anomalies of the face and have multifactorial etiology, with both environmental and genetic risk factors playing crucial roles. Though at least 40 loci have attained genomewide significant association with nonsyndromic CL/P, these loci largely reside in noncoding regions of the human genome, and subsequent resequencing studies of neighboring candidate genes have revealed only a limited number of etiologic coding variants. The present study was conducted to identify etiologic coding variants in GREM1, a locus that has been shown to be largely associated with cleft of both lip and soft palate. Patients and Method: We resequenced DNA from 397 sub-Saharan Africans with CL/P and 192 controls using Sanger sequencing. Following analyses of the sequence data, we observed 2 novel coding variants in GREM1. These variants were not found in the 192 African controls and have never been previously reported in any public genetic variant database that includes more than 5000 combined African and African American controls or from the CL/P literature. Results: The novel variants include p.Pro164Ser in an individual with soft palate cleft only and p.Gly61Asp in an individual with bilateral cleft lip and palate. The proband with the p.Gly61Asp GREM1 variant is a van der Woude (VWS) case who also has an etiologic variant in IRF6 gene. Conclusion: Our study demonstrated that there is low number of etiologic coding variants in GREM1,Objective: Cleft lip and/or cleft palate (CL/P) are congenital anomalies of the face and have multifactorial etiology, with both environmental and genetic risk factors playing crucial roles. Though at least 40 loci have attained genomewide significant association with nonsyndromic CL/P, these loci largely reside in noncoding regions of the human genome, and subsequent resequencing studies of neighboring candidate genes have revealed only a limited number of etiologic coding variants. The present study was conducted to identify etiologic coding variants in GREM1, a locus that has been shown to be largely associated with cleft of both lip and soft palate. Patients and Method: We resequenced DNA from 397 sub-Saharan Africans with CL/P and 192 controls using Sanger sequencing. Following analyses of the sequence data, we observed 2 novel coding variants in GREM1. These variants were not found in the 192 African controls and have never been previously reported in any public genetic variant database that includes more than 5000 combined African and African American controls or from the CL/P literature. Results: The novel variants include p.Pro164Ser in an individual with soft palate cleft only and p.Gly61Asp in an individual with bilateral cleft lip and palate. The proband with the p.Gly61Asp GREM1 variant is a van der Woude (VWS) case who also has an etiologic variant in IRF6 gene. Conclusion: Our study demonstrated that there is low number of etiologic coding variants in GREM1, confirming earlier suggestions that variants in regulatory elements may largely account for the association between this locus and CL/P. … (more)
- Is Part Of:
- Cleft palate-craniofacial journal. Volume 55:Number 5(2018)
- Journal:
- Cleft palate-craniofacial journal
- Issue:
- Volume 55:Number 5(2018)
- Issue Display:
- Volume 55, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 55
- Issue:
- 5
- Issue Sort Value:
- 2018-0055-0005-0000
- Page Start:
- 736
- Page End:
- 742
- Publication Date:
- 2018-05
- Subjects:
- GREM1 gene -- cleft lip and/or cleft palate -- soft palate cleft -- sub-Saharan Africans -- DNA sequencing
Cleft palate -- Periodicals
Skull -- Abnormalities -- Periodicals
Cranial manipulation -- Periodicals
Skull -- Abnormalities -- Surgery -- Periodicals
Face -- Abnormalities -- Surgery -- Periodicals
Fente palatine -- Périodiques
Crâne -- Malformations -- Périodiques
Manipulation crânienne -- Périodiques
Crâne -- Malformations -- Chirurgie -- Périodiques
Face -- Malformations -- Chirurgie -- Périodiques
Cleft palate
Cranial manipulation
Face -- Abnormalities -- Surgery
Skull -- Abnormalities
Skull -- Abnormalities -- Surgery
Cleft Lip
Cleft Palate
Facial Bones -- abnormalities
Skull -- abnormalities
Periodicals
Periodicals
Periodicals
617.522 - Journal URLs:
- http://cpcj.allenpress.com ↗
http://journals.sagepub.com/home/cpca ↗
http://www.sagepublications.com/ ↗
http://cleftpalatejournal.pitt.edu/ojs/cleftpalate/issue/archive ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1055-6656;screen=info;ECOIP ↗ - DOI:
- 10.1177/1055665618754948 ↗
- Languages:
- English
- ISSNs:
- 1055-6656
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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