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Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia


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Tong, Dan; Colley, Deanne; Thoo, Renee; Li, Tony Y; Plante, Isabelle ORCID logoORCID: https://orcid.org/0000-0003-2080-6450; Laird, Dale W; Bai, Donglin et Kidder, Gerald M. (2009). Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia Disease Models and Mechanisms , vol. 2 , nº 3-4. pp. 157-171. DOI: 10.1242/dmm.000935.

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The essential role of connexin43 (Cx43) during oogenesis has been demonstrated by the severe germ cell deficiency and arrested folliculogenesis observed in Cx43 knockout mice. Recently, another mutant mouse strain became available (Gja1(Jrt)/+) that carries the dominant loss-of-function Cx43 mutation, Cx43(G60S). Gja1(Jrt)/+ mice display features of the human disease oculodentodigital dysplasia (ODDD), which is caused by mutations in the GJA1 gene. We used this new mutant strain to study how a disease-linked Cx43 mutant affects oogenesis. We found that female mutant mice are subfertile with significantly reduced mating success and small litters. The phosphorylated species of the Cx43 protein are reduced in the mutant ovaries in association with impaired trafficking and assembly of gap junctions in the membranes of granulosa cells, confirming that the mutant protein acts dominantly on its wild-type counterpart. Correspondingly, although starting with a normal abundance of germ cells, ovaries of the mutant mice contain significantly fewer pre-ovulatory follicles and do not respond to superovulation by gonadotropins, which is at least partially the result of reduced proliferation and increased apoptosis of granulosa cells. We conclude that the Gja1(Jrt) mutation has a dominant negative effect on Cx43 function in the ovary, rendering the females subfertile. Given these findings, closer examination of reproductive function in ODDD human females is warranted.

Type de document: Article
Mots-clés libres: -
Centre: Centre INRS-Institut Armand Frappier
Date de dépôt: 01 juill. 2024 03:21
Dernière modification: 01 juill. 2024 03:21
URI: https://espace.inrs.ca/id/eprint/15212

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