Sex genotyping of mice
While adult mice can be readily sexed using anatomical features, young male and female mouse embryos are not yet sufficiently developed to assess their sex. In fact, their genital tubercles look superficially identical. At E16, only about 4 days before birth, the tubercle looks like this: E16 genital tubercles in Baskin's book, p. 108, figure 2.
If the sex cannot be determined by inspection, a genotyping PCR for any region only found on the Y chromosome [1] can be used.
Common male-specific PCRs
Sry Sex-determining region of the Y chromosome [2]
- forward SRY F : TTG TCT AGA GAG CAT GGA GGG CCA TGT CAA
- reverse SRY R : CCA CTC CTC TGT GAC ACT TTA GCC CTC CGA
- PCR product: 273 base pair
- forward sry1 AACAACTGGGCTTTGCACATTG
- reverse sry2 GTTTATCAGGGTTTCTCTCTAGC
- PCR product: 146/166 bp doublet
Homologous pair SmcX/SmcY
- SMCX-1 5'-CCGCTGCCAAATTCTTTGG-3'
- SMC4-1 5'-TGAAGCTTTTGGCTTTGAG-3'
- PCR product: females single band, males 2 bands because of an intron difference between the X and Y genes (Agulnik 1997, PMID 9060413); adapted from Case Western Transgenic Facility
Test PCR with adult tail genomic samples
Conditions: Templates are known adult male and female tail gDNA samples. Standard PCR cycled using progressively lowered annealing temperature (65-58°C for first cycles, then 58°C); same conditions for all reactions. Primers as listed above. 12μL of a 25μL + 5μL Orange G run on a 2% agarose gel.
Interpretation: The sry F/R pair worked best but does show weak unspecific products of similar size as the male-specific 273bp band. The sry 1/2 pair is probably also specific but bands are harder to recognise. For the SMC, we didn't observe the described doublet expected in males.
Keep in mind that this is a standard PCR. Amplification and specificity can probably be increased by optimisation of the PCR reaction.
