mortality/aging
• fewer than expected mice are born
|
reproductive system
• by P20, male germ cells are reduced compared to in wild-type mice
|
• narrower than in wild-type mice
|
small testis
(
J:159793
)
|
• mice exhibit variably defective spermatogenesis compared to in wild-type mice
• postmeiotic cells types are missing compared to in wild-type mice
• a few mice exhibit more severe defects in spermatogenesis compared with wild-type mice with agametic testes
|
• median epididymal sperm count is reduced compared to in wild-type mice
|
• mice exhibit impaired chromosome synapsis during male meiosis unlike wild-type mice
• univalent chromosomes in metaphase I indicate a defect in formation or maintenance of chiasmata in post-pachytene spermatocytes unlike in wild-type mice
|
• in homozygous female mice compared with heterozygous female mice
|
• testes exhibit over-expression of endogenous retrotransposable elements compared to in wild-type mice
|
• pachytene and metaphase I spermatocytes undergo apoptosis unlike in wild-type mice
• increases in apoptosis is observed at P19 to P22 and P29 to P31 but not at P16
|
• severe
|
endocrine/exocrine glands
• narrower than in wild-type mice
|
small testis
(
J:159793
)
|
cellular
• by P20, male germ cells are reduced compared to in wild-type mice
|
• median epididymal sperm count is reduced compared to in wild-type mice
|
• mice exhibit impaired chromosome synapsis during male meiosis unlike wild-type mice
• univalent chromosomes in metaphase I indicate a defect in formation or maintenance of chiasmata in post-pachytene spermatocytes unlike in wild-type mice
|
• pachytene and metaphase I spermatocytes undergo apoptosis unlike in wild-type mice
• increases in apoptosis is observed at P19 to P22 and P29 to P31 but not at P16
|