Literature DB >> 17097888

Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.

D W Meechan1, T M Maynard, Y Wu, D Gopalakrishna, J A Lieberman, A-S LaMantia.   

Abstract

We evaluated the consequences of heterozygous chromosome 22q11 deletion - a significant genetic risk for schizophrenia - for expression levels and patterns of a subset of 22q11 genes implicated in schizophrenia and other phenotypes in mouse models of 22q11 deletion syndrome (22q11DS). In deleted embryos, expression levels of at least nine 22q11 orthologues decline by 40-60% in the frontonasal mass/forebrain and other 22q11DS phenotypic sites (branchial and aortic arches, limb buds); however, coincident expression patterns of 22q11 and Snail genes - diagnostic for neural crest-derived mesenchyme - are unchanged, and Snail1 expression levels do not decline. Subsequently, 22q11 mRNA levels are reduced by 40-60% in the brains of developing, adolescent and adult deleted mice without altered expression patterns, dysmorphology or reduced cell density. Apparently, in deleted individuals, 22q11 gene expression declines across otherwise stable cell populations, perhaps disrupting individual cell function via diminished dosage. Such changes might contribute to schizophrenia vulnerability in 22q11DS.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17097888     DOI: 10.1016/j.mcn.2006.09.001

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  26 in total

1.  Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.

Authors:  Daniel W Meechan; Eric S Tucker; Thomas M Maynard; Anthony-Samuel LaMantia
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-10       Impact factor: 11.205

2.  No evidence for parental imprinting of mouse 22q11 gene orthologs.

Authors:  Thomas M Maynard; Daniel W Meechan; Clifford C Heindel; Amanda Z Peters; Robert M Hamer; Jeffrey A Lieberman; Anthony-Samuel LaMantia
Journal:  Mamm Genome       Date:  2006-08-04       Impact factor: 2.957

Review 3.  Molecular mechanisms in 22q11 deletion syndrome.

Authors:  Nigel M Williams
Journal:  Schizophr Bull       Date:  2011-09       Impact factor: 9.306

4.  Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.

Authors:  Elizabeth M Paronett; Daniel W Meechan; Beverly A Karpinski; Anthony-Samuel LaMantia; Thomas M Maynard
Journal:  Cereb Cortex       Date:  2014-12-01       Impact factor: 5.357

Review 5.  Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Authors:  Daniel W Meechan; Thomas M Maynard; Eric S Tucker; Alejandra Fernandez; Beverly A Karpinski; Lawrence A Rothblat; Anthony-S LaMantia
Journal:  Prog Neurobiol       Date:  2015-04-09       Impact factor: 11.685

Review 6.  Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.

Authors:  D W Meechan; T M Maynard; E S Tucker; A-S LaMantia
Journal:  Int J Dev Neurosci       Date:  2010-09-15       Impact factor: 2.457

7.  22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.

Authors:  Thomas M Maynard; Deepak Gopalakrishna; Daniel W Meechan; Elizabeth M Paronett; Jason M Newbern; Anthony-Samuel LaMantia
Journal:  Hum Mol Genet       Date:  2012-10-16       Impact factor: 6.150

Review 8.  Losing your inhibition: linking cortical GABAergic interneurons to schizophrenia.

Authors:  Melis Inan; Timothy J Petros; Stewart A Anderson
Journal:  Neurobiol Dis       Date:  2012-11-29       Impact factor: 5.996

Review 9.  Schizophrenia and 22q11.2 deletion syndrome.

Authors:  Anne S Bassett; Eva W C Chow
Journal:  Curr Psychiatry Rep       Date:  2008-04       Impact factor: 5.285

Review 10.  When half is not enough: gene expression and dosage in the 22q11 deletion syndrome.

Authors:  D W Meechan; T M Maynard; D Gopalakrishna; Y Wu; A S LaMantia
Journal:  Gene Expr       Date:  2007
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.