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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Aurkatm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:6718894
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Aurkatm1c(EUCOMM)Hmgu/Aurkatm1c(EUCOMM)Hmgu
Tg(Gdf9-icre)5092Coo/0
involves: C57BL/6 * C57BL/6J * C57BL/6N MGI:7284072


Genotype
MGI:7284072
cn1
Allelic
Composition
Aurkatm1c(EUCOMM)Hmgu/Aurkatm1c(EUCOMM)Hmgu
Tg(Gdf9-icre)5092Coo/0
Genetic
Background
involves: C57BL/6 * C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aurkatm1c(EUCOMM)Hmgu mutation (0 available); any Aurka mutation (40 available)
Tg(Gdf9-icre)5092Coo mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• after induction of ovulation with PMSG plus hCG, none of the cells harvested from the oviducts have polar bodies, and all cells are arrested in Metaphase I (Met I) indicating a failure to complete meiosis I (MI)
• in vitro, prophase I-arrested oocytes fail to undergo polar body extrusion after maturation; however, the % of oocytes that resume meiosis and undergo nuclear envelope breakdown in vitro is normal
• exogenous AURKA-EGFP expression rescues nearly all oocytes, restoring their ability to extrude polar bodies and reach Metaphase of meiosis II (Met II); in contrast, ectopic expression of AURKB-EGFP or AURKC-EYFP fails to rescue MI failure and none of these oocytes extrude a polar body
• in vitro, oocytes exhibit a delay in resolving individual chromosomes during meiotic maturation and show defects in MI spindle building, with inability to fragment aMTOCs (acentriolar multiple microtubule-organizing centers) upon exiting from prophase I and loss of localized TACC3 protein (a known AURKA substrate required for spindle building)
• 55% of oocytes show monopolar spindles while ~45% have short bipolar spindles with significantly reduced spindle length and volume at Met I
• exogenous expression of AURKA rescues MI spindle volume and restores chromosome resolution to wild-type like kinetics, resulting in stable, bipolar MI spindle formation; in contrast, expression of AURKB-EGFP fails to rescue all of these parameters whereas AURKC-EYFP partially rescues the time to spindle bipolarization
• at 2 months of age, ovaries contain about half the number of corpora lutea (CL) observed in wild-type ovaries
• however, follicle development and ovulation are normal, and no statistically significant reduction in CL number seen at 6 months of age
• sexually mature females mated with age-matched wild-type male mice of proven fertility never produced a pup during a 4-month fertility trial

endocrine/exocrine glands
• at 2 months of age, ovaries contain about half the number of corpora lutea (CL) observed in wild-type ovaries
• however, follicle development and ovulation are normal, and no statistically significant reduction in CL number seen at 6 months of age

cellular
• after induction of ovulation with PMSG plus hCG, none of the cells harvested from the oviducts have polar bodies, and all cells are arrested in Metaphase I (Met I) indicating a failure to complete meiosis I (MI)
• in vitro, prophase I-arrested oocytes fail to undergo polar body extrusion after maturation; however, the % of oocytes that resume meiosis and undergo nuclear envelope breakdown in vitro is normal
• exogenous AURKA-EGFP expression rescues nearly all oocytes, restoring their ability to extrude polar bodies and reach Metaphase of meiosis II (Met II); in contrast, ectopic expression of AURKB-EGFP or AURKC-EYFP fails to rescue MI failure and none of these oocytes extrude a polar body
• in vitro, oocytes exhibit a delay in resolving individual chromosomes during meiotic maturation and show defects in MI spindle building, with inability to fragment aMTOCs (acentriolar multiple microtubule-organizing centers) upon exiting from prophase I and loss of localized TACC3 protein (a known AURKA substrate required for spindle building)
• 55% of oocytes show monopolar spindles while ~45% have short bipolar spindles with significantly reduced spindle length and volume at Met I
• exogenous expression of AURKA rescues MI spindle volume and restores chromosome resolution to wild-type like kinetics, resulting in stable, bipolar MI spindle formation; in contrast, expression of AURKB-EGFP fails to rescue all of these parameters whereas AURKC-EYFP partially rescues the time to spindle bipolarization





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory