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Haploinsufficiency of Homeodomain Proteins Six3, Vax1, and Otx2 Causes Subfertility in Mice via Distinct Mechanisms.

Citation
Hoffmann, H. M., et al. “Haploinsufficiency Of Homeodomain Proteins Six3, Vax1, And Otx2 Causes Subfertility In Mice Via Distinct Mechanisms.”. Neuroendocrinology, pp. 200-207.
Center UCSD-UCLA
Author Hanne M Hoffmann, Erica C Pandolfi, Rachel Larder, Pamela L Mellon
Keywords heterozygous, Homeodomain, Infertility
Abstract

Haploinsufficiency occurs when loss of one copy of a diploid gene (hemizygosity) causes a phenotype. It is relatively rare, in that most genes can produce sufficient mRNA and protein from a single copy to prevent any loss of normal activity and function. Reproduction is a complex process relying on migration of GnRH neurons from the olfactory placode to the hypothalamus during development. We have studied 3 different homeodomain genes Otx2, Vax1, and Six3 and found that the deletion of one allele for any of these genes in mice produces subfertility or infertility in one or both sexes, despite the presence of one intact allele. All 3 heterozygous mice have reduced numbers of GnRH neurons, but the mechanisms of subfertility differ significantly. This review compares the subfertility phenotypes and their mechanisms.

Year of Publication
2019
Journal
Neuroendocrinology
Volume
109
Issue
3
Number of Pages
200-207
Date Published
12/2019
ISSN Number
1423-0194
DOI
10.1159/000494086
Alternate Journal
Neuroendocrinology
PMID
30261489
PMCID
PMC6437011
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