The proportion of progeny expected to be
in the testcross of
, considering the given recombination frequencies and an interference value of 24%, is approximately 76.09%.
To determine the proportion of
we need to consider genetic linkage, recombination frequencies, and the concept of interference. Let's break it down step by step:
1. Understanding the Cross:
- The initial cross is between two homozygous individuals with the genotype

- A testcross involves crossing these F1 progeny with a homozygous recessive individual. However, since the problem doesn't specify the recessive alleles, we'll assume it's the same genotype
2. Genetic Map
- The map distance between genes a and b is 16 cM (centiMorgans), and between b and c is 9 cM.
3. Recombination Frequency:
- The recombination frequency between genes is approximately equal to the map distance (in cM) divided by 100. Therefore, the recombination frequency between a and b is 16%, and between b and c is 9%.
4. Interference and Coincidence:
- Interference is the phenomenon where a crossover in one region of a chromosome inhibits crossovers in an adjacent region. It's calculated as
where coincidence is the observed double crossover rate divided by the expected double crossover rate.
- Here, we have an interference of 24%, meaning the actual double crossover events are reduced by this amount.
5. Calculating Expected Double Crossovers:
- The expected double crossover frequency (without interference) between a and c is the product of the individual frequencies:
or 1.44%.
- With 24% interference, the actual double crossover frequency is
6. Proportion of abc/abc Progeny:
- The progeny with the
genotype result from either no crossover events or double crossovers between a and c .
- The probability of no crossovers is simply the complement of any crossovers occurring, which is

Let's calculate the exact proportion of
progeny expected:
The proportion of progeny expected to be
in the testcross of
, considering the given recombination frequencies and an interference value of 24%, is approximately 76.09%. This accounts for both scenarios where no crossover events occur and scenarios involving double crossovers between genes a and c .