Abstract
Genomic imprinting results in preferential gene expression from paternally versus maternally inherited chromosomes. We used a genome-wide approach to uncover sex-specific parent-of-origin allelic effects in the adult mouse brain. Our study identified preferential selection of the maternally inherited X chromosome in glutamatergic neurons of the female cortex. Moreover, analysis of the cortex and hypothalamus identified 347 autosomal genes with sex-specific imprinting features. In the hypothalamus, sex-specific imprinted genes were mostly found in females, which suggests parental influence over the hypothalamic function of daughters. We show that interleukin-18, a gene linked to diseases with sex-specific prevalence, is subject to complex, regional, and sex-specific parental effects in the brain. Parent-of-origin effects thus provide new avenues for investigation of sexual dimorphism in brain function and disease.
MeSH Terms
Alleles
Animals
Crosses, Genetic
Dioxygenases
Epigenesis, Genetic
Female
Gene Expression Profiling
Genes, X-Linked
Genomic Imprinting
Glutamic Acid/metabolism
Interleukin-18/genetics
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Mitochondrial Proteins/genetics
Neurons/metabolism
Oxygenases/genetics
Polymorphism, Single Nucleotide
Prefrontal Cortex/cytology,metabolism
Preoptic Area/cytology,metabolism
Ribosomal Proteins/genetics
Sex Characteristics
Succinate Dehydrogenase/genetics
X Chromosome Inactivation
Chemicals
Interleukin-18
Mitochondrial Proteins
Ribosomal Proteins
Glutamic Acid
Oxygenases
Dioxygenases
Bco2 protein, mouse
Succinate Dehydrogenase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Gregg Christopher
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Zhang Jiangwen
Butler James E
Haig David
Dulac Catherine
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