Characterization of meiotic recombination intermediates through gene knockouts in founder hybrid mice

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Figure 2.
Figure 2.

Investigation of fertility phenotypes of Dmc1 hybrid founder mice. (A) Representative immunofluorescence staining of DMC1 (red) in testis nuclear spreads from two founder mice, one with DMC1 present (Dmc1+/+) and with DMC1 ablated (Dmc1−/−) with costaining of the synaptonemal complex protein SYCP3, which labels the chromosome axis (green) in zygotene (top panels) and pachytene/pseudo-pachytene (middle panels). Lower panels show pachytene/pseudo-pachytene stage staining of SYCP1 (red), labeling the synaptonemal-complex transverse filament, and SYCP3 (green) staining of the chromosome axes. Pronounced asynapsis is visible in a founder with ablated DMC1 (Dmc1−/−). (B,C) Fertility parameters for the founder mice showing complete ablation of DMC1 (Dmc1−/−; n = 7) with age-matched wild-type B6CASTF1 mice (Dmc1+/+; n = 10), with normalized testis weight (B) and total caudal sperm count (C).

This Article

  1. Genome Res. 33: 2018-2027

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