Small 6q16.1 deletions encompassing POU3F2 cause susceptibility to obesity and variable developmental delay with intellectual disability

Kasher, Paul R. and Shertz, Katherine E. and Thomas, Megan and Jackson, Adam and Annunziata, Silvia and Ballesta-Martinez, Maria J. and Campeau, Philippe M. and Clayton, Peter E. and Eaton, Jennifer L. and Granata, Tiziana and Guille-Navarro, Encarna and Hernando, Cristina and Laverriere, Caroline E. and Lieden, Agne and Villa-Marcos, Olaya and McEntagart, Meriel and Nordgren, Ann and Pantaleonie, Chiara and Prebel-Richard, Celine and Sarret, Catherine and Sciacca, Francesca L. and Wright, Ronnie and Kerr, Bronwyn and Glasgow, Eric and Banka, Siddharth (2016) Small 6q16.1 deletions encompassing POU3F2 cause susceptibility to obesity and variable developmental delay with intellectual disability. American Journal of Human Genetics, 98 (2). pp. 363-372. ISSN 0002-9297

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Abstract

Genetic studies of intellectual disability and identification of monogenic causes of obesity in humans have made immense contribution toward the understanding of the brain and control of body mass. The leptin > melanocortin > SIM1 pathway is dysregulated in multiple monogenic human obesity syndromes but its downstream targets are still unknown. In ten individuals from six families, with overlapping 6q16.1 deletions, we describe a disorder of variable developmental delay, intellectual disability, and susceptibility to obesity and hyperphagia. The 6q16.1 deletions segregated with the phenotype in multiplex families and were shown to be de novo in four families, and there was dramatic phenotypic overlap among affected individuals who were independently ascertained without bias from clinical features. Analysis of the deletions revealed a ∼350 kb critical region on chromosome 6q16.1 that encompasses a gene for proneuronal transcription factor POU3F2, which is important for hypothalamic development and function. Using morpholino and mutant zebrafish models, we show that POU3F2 lies downstream of SIM1 and controls oxytocin expression in the hypothalamic neuroendocrine preoptic area. We show that this finding is consistent with the expression patterns of POU3F2 and related genes in the human brain. Our work helps to further delineate the neuro-endocrine control of energy balance/body mass and demonstrates that this molecular pathway is conserved across multiple species.

Item Type:
Journal Article
Journal or Publication Title:
American Journal of Human Genetics
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/2700/2716
Subjects:
ID Code:
78556
Deposited By:
Deposited On:
15 Aug 2016 12:36
Refereed?:
Yes
Published?:
Published
Last Modified:
16 Nov 2020 06:29