Autosomal aneuploidy in mice: generation and developmental consequences
- PMID: 3530382
- DOI: 10.1016/0361-9230(86)90075-4
Autosomal aneuploidy in mice: generation and developmental consequences
Abstract
Spontaneous aneuploidy in the mouse is uncommon, but specific mating schemes have been developed that produce aneuploid conceptuses at high frequencies. The most commonly reported aneuploid condition in the mouse is autosomal trisomy, in which there is an extra copy (in whole or in part) of a chromosome. In this review, we present several of the schemes used in producing trisomic, partially (tertiary) trisomic, and monosomic conceptuses and summarize the developmental consequences that are associated with each of the autosomal trisomies of the mouse.
Similar articles
-
Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4500-5. doi: 10.1073/pnas.0500802102. Epub 2005 Mar 8. Proc Natl Acad Sci U S A. 2005. PMID: 15755806 Free PMC article.
-
Developmental consequences of autosomal aneuploidy in mammals.Dev Genet. 1987;8(4):249-65. doi: 10.1002/dvg.1020080408. Dev Genet. 1987. PMID: 2971493 Review.
-
Production of viable adult trisomy 17 reversible diploid mouse chimeras.Proc Natl Acad Sci U S A. 1982 Jul;79(14):4376-80. doi: 10.1073/pnas.79.14.4376. Proc Natl Acad Sci U S A. 1982. PMID: 6956868 Free PMC article.
-
Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): production of viable trisomy 16 diploid mouse chimeras.Dev Biol. 1984 Feb;101(2):416-24. doi: 10.1016/0012-1606(84)90156-8. Dev Biol. 1984. PMID: 6229437
-
Mouse models of aneuploidy to understand chromosome disorders.Mamm Genome. 2022 Mar;33(1):157-168. doi: 10.1007/s00335-021-09930-z. Epub 2021 Nov 1. Mamm Genome. 2022. PMID: 34719726 Free PMC article. Review.
Cited by
-
A unique downregulation of h2-calponin gene expression in Down syndrome: a possible attenuation mechanism for fetal survival by methylation at the CpG island in the trisomic chromosome 21.Mol Cell Biol. 1997 Feb;17(2):707-12. doi: 10.1128/MCB.17.2.707. Mol Cell Biol. 1997. PMID: 9001224 Free PMC article.
-
Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome.PLoS One. 2010 Jul 16;5(7):e11561. doi: 10.1371/journal.pone.0011561. PLoS One. 2010. PMID: 20661276 Free PMC article.
-
Nerve growth factor corrects developmental impairments of basal forebrain cholinergic neurons in the trisomy 16 mouse.Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1793-7. doi: 10.1073/pnas.88.5.1793. Proc Natl Acad Sci U S A. 1991. PMID: 2000385 Free PMC article.
-
Molecular genetic analysis of Down syndrome.Hum Genet. 2009 Jul;126(1):195-214. doi: 10.1007/s00439-009-0696-8. Epub 2009 Jun 13. Hum Genet. 2009. PMID: 19526251 Review.
-
Blastomere karyotyping and transfer of chromosomally selected embryos. Implications for the production of specific animal models and human prenatal diagnosis.Hum Genet. 1988 Dec;80(4):333-6. doi: 10.1007/BF00273646. Hum Genet. 1988. PMID: 3198110
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases