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. 2020 May 26;103(2):183–194. doi: 10.1093/biolre/ioaa083

Figure 5.

Figure 5

Phenotypic analysis of 4921507P07Rik knockout male mice. (A) Genomic structure and knockout strategy of mouse 4921507P07Rik. Two sgRNAs were designed to target the first coding exon (Exon 2) and the 3′ UTR region of the last coding exon (Exon 10). Three primers (Fw1, Rv1, and Rv2) were designed for genotyping. (B) Mutant and wild-type alleles were detected by genomic PCR using primer sets Fw1–Rv2 and Fw1–Rv1, respectively. (C) DNA sequence of the knockout allele was determined by Sanger sequencing. (D) Testis appearance and testis to body weight ratios of 4921507P07Rik heterozygous and homozygous knockout mice. Scale bar = 2 mm. (E) Histological analyses of testes and epididymides in 4921507P07Rik heterozygous and homozygous knockout mice. Scale bars = 50 μm. (F) Morphology of cauda epididymal spermatozoa in 4921507P07Rik heterozygous and homozygous knockout mice. Scale bars = 20 μm. (G) Analysis of sperm motility in 4921507P07Rik heterozygous and homozygous knockout mice. Sperm motility and kinetic parameters were measured at 10 and 120 min of incubation in TYH media.