RRC ID 34774
Author Takagi T, Nishizaki Y, Matsui F, Wakamatsu N, Higashi Y.
Title De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.
Journal Hum. Mol. Genet.
Abstract Mowat-Wilson syndrome (MOWS) is caused by de novo heterozygous mutation at ZEB2 (SIP1, ZFHX1B) gene, and exhibit moderate to severe intellectual disability (ID), a characteristic facial appearance, epilepsy and other congenital anomalies. Establishing a murine MOWS model is important, not only for investigating the pathogenesis of this disease, but also for identifying compounds that may improve the symptoms. However, because the heterozygous Zeb2 knockout mouse could not be maintained as a mouse line with the inbred C57BL/6 background, it was difficult to use those mice for the study of MOWS. Here, we systematically generated de novo Zeb2 Δex7/+ mice by inducing the Zeb2 mutation in the germ cells using conditional recombination system. The de novo Zeb2 Δex7/+ mice with C57BL/6 background developed multiple defects relevant to MOWS, including craniofacial abnormalities, defective corpus callosum formation and the decreased number of parvalbumin interneurons in the cortex. In behavioral analyses, these mice showed reduced motor activity, increased anxiety and impaired sociability. Notably, during the Barnes maze test, immobile Zeb2 mutant mice were observed over repeated trials. In contrast, neither the mouse line nor the de novo Zeb2 Δex7/+ mice with the closed colony ICR background showed cranial abnormalities or reduced motor activities. These results demonstrate the advantages of using de novo Zeb2 Δex7/+ mice with the C57BL/6 background as the MOWS model. To our knowledge, this is the first time an inducible de novo mutation system has been applied to murine germline cells to produce an animal model of a human congenital disease.
Volume 24(22)
Pages 6390-402
Published 2015-11-15
DOI 10.1093/hmg/ddv350
PII ddv350
PMID 26319231
MeSH Aicardi Syndrome / genetics Aicardi Syndrome / metabolism Animals Cerebral Cortex / metabolism Craniofacial Abnormalities / genetics Craniofacial Abnormalities / metabolism Disease Models, Animal Epilepsy / genetics Epilepsy / metabolism Facies Female Genetic Association Studies Germ Cells Germ-Line Mutation Heterozygote Hirschsprung Disease / genetics* Hirschsprung Disease / metabolism Homeodomain Proteins / genetics* Homeodomain Proteins / metabolism* Humans Intellectual Disability / genetics* Intellectual Disability / metabolism Male Mental Disorders / genetics Mental Disorders / metabolism Mice Mice, Inbred C57BL Mice, Inbred ICR Mice, Knockout Microcephaly / genetics* Microcephaly / metabolism Repressor Proteins / genetics* Repressor Proteins / metabolism* Zinc Finger E-box Binding Homeobox 2
IF 4.902
Times Cited 3
WOS Category GENETICS & HEREDITY BIOCHEMISTRY & MOLECULAR BIOLOGY
Resource
Mice Emx1-Cre KI delta neo(RBRC01345)