Answers recombination
From Wikionchus
- Phenotypically "wild type" animals are heterozygous for both mutations
- In a fraction of meioses cross-over events took place that separated the two mutants. This happened when the heterozygous animal, which was a male here, made its sperm. Strictly speaking, this type of cross only examines recombination rates in male spermatogenesis, which might be different than what happens in the hermaphrodite.
- Determination of the recombination frequency in a F1-backcross:
We are looking at 1 potentially recombined gamete per animal, thus we can write:
| recombinant gametes | 4+6=10 |
| non-recombinant gametes | 77+73=150 |
| rec. fraction r | 10/160=0.063 |
- If always exactly one recombination happens per meiosis you might think r should be 100%. It is not, because only 2 out of 4 gametes will receive a recombined chromatid. (Cross-over takes place between the two "neighbouring" non-sister-chromatids in Meiosis I, the two "outward" chromatids are unaffected!)
- Recombination fractions in most organisms are not additive. This is because there are double cross-overs: Two loci on different chromosome ends can seemingly be un-recombined in some animals (e.g. both wild type in our example) , when two (or 4,6...) recombinations took place between the loci. Double cross-over is the more likely the further apart two loci are on a chromosome. Recombination fractions can be approximately made additive by transforming them to centiMorgan as a map unit.
- Additional question: In C. elegans no chromosome is bigger than 50cM. Why could that be?
- Remark: In daily practice you will usually do an F2-mapping by genotyping progeny from a selfed F1. Also our linkage map was constructed that way. I chose another example here because calculation of recombination frequencies in a F2 population is a bit advanced...thats what computers are for!
