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Title: Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
Authors: Lindgren, Amelia M ×
Hoyos, Tatiana
Talkowski, Michael E
Hanscom, Carrie
Blumenthal, Ian
Chiang, Colby
Ernst, Carl
Pereira, Shahrin
Ordulu, Zehra
Clericuzio, Carol
Drautz, Joanne M
Rosenfeld, Jill A
Shaffer, Lisa G
Velsher, Lea
Pynn, Tania
Vermeesch, Joris
Harris, David J
Gusella, James F
Liao, Eric C
Morton, Cynthia C #
Issue Date: May-2013
Publisher: Springer-Verlag
Series Title: Human Genetics vol:132 issue:5 pages:537-552
Abstract: We describe a female subject (DGAP100) with a 46,X,t(X;5)(p11.3;q35.3)inv(5)(q35.3q35.1)dn, severe psychomotor retardation with hypotonia, global postnatal growth restriction, microcephaly, globally reduced cerebral volume, seizures, facial dysmorphia and cleft palate. Fluorescence in situ hybridization and whole-genome sequencing demonstrated that the X chromosome breakpoint disrupts KDM6A in the second intron. No genes were directly disrupted on chromosome 5. KDM6A is a histone 3 lysine 27 demethylase and a histone 3 lysine 4 methyltransferase. Expression of KDM6A is significantly reduced in DGAP100 lymphoblastoid cells compared to control samples. We identified nine additional cases with neurodevelopmental delay and various other features consistent with the DGAP100 phenotype with copy number variation encompassing KDM6A from microarray databases. We evaluated haploinsufficiency of kdm6a in a zebrafish model. kdm6a is expressed in the pharyngeal arches and ethmoid plate of the developing zebrafish, while a kdm6a morpholino knockdown exhibited craniofacial defects. We conclude KDM6A dosage regulation is associated with severe and diverse structural defects and developmental abnormalities.
URI: 
ISSN: 0340-6717
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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