Final answer:
The statement that genetic mapping assumes recombination can occur at any point along a chromosome with equal probability is false. While this assumption was foundational for early chromosome mapping, in reality, recombination rates can vary due to hotspots and genomic regions less prone to recombination. False is the correct answer.
Step-by-step explanation:
Genetic mapping indeed assumes that recombination can occur at any point along a chromosome with equal probability; however, this is not entirely accurate in reality. Alfred Sturtevant, in constructing chromosome maps, postulated that recombination frequency—the average number of crossovers between two alleles—correlated with their genetic distance from each other.
This meant that more distant alleles had a higher chance of recombining since there was a larger region over which recombination could occur. Nearby alleles, on the other hand, were likely to be inherited together.
Sturtevant represented alleles in a linear map and defined genetic distances in map units or centimorgans (cM). A recombination frequency of 0.01 would correspond to a distance of 1 cM. While genes could range from being perfectly linked (recombination frequency = 0) to perfectly unlinked (recombination frequency = 0.5), this model assumes uniform recombination along the chromosome.
However, real-world observations have shown that some parts of the genome are recombination hotspots, while others are less prone to recombination, which challenges the equal probability assumption.
In summary, the initial statement is False because although genetic mapping assumes an equal likelihood of recombination along chromosomes, practical evidence reveals that this is not the case due to the presence of recombination hotspots and regions with low recombination activity.