Why are double-crossover events expected less frequently than single-crossover events?

Short Answer

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Answer: Double-crossover events are less frequent than single-crossover events due to the relationship between gene positioning on a chromosome, the probability of crossover occurrence, and the effect of interference. Double-crossover events require two separate crossover events to occur in close proximity, which is less likely than a single crossover. Moreover, the phenomenon of interference reduces the probability of a second crossover event happening nearby, ensuring that genetic recombination occurs fairly evenly across the entire length of the chromosome.

Step by step solution

01

Understand Genetic Recombination

Genetic recombination is the process by which genetic material is exchanged between homologous chromosomes during meiosis, the cell division process that produces gametes (sperm and egg cells). This exchange is essential for genetic diversity and allows offspring to inherit a unique combination of genes from their parents.
02

Learn about Crossover Events

Crossover events occur during the first stage of meiosis, known as prophase I. This is when homologous chromosomes pair up and align themselves side-by-side. The process of crossover involves the breaking and rejoining of homologous DNA segments between the paired chromosomes. When a single crossover event happens, it causes two of the four chromatids to exchange genetic material, while the other two remain unchanged.
03

Understand Double-crossover events

Double-crossover events happen when two crossover events occur between the same pair of homologous chromosomes. In this case, two separate segments of the paired chromosomes switch places with each other. While it may seem like double crossover events would be more frequent than single crossover events, this is not the case.
04

The Probability of Crossover Events

The more closely positioned two genes are along a chromosome, the less likely they are to experience a crossover event between them. This is because the likelihood of a crossover occurring is directly related to the physical distance between two genes on a chromosome. Since double-crossover events require two separate crossover events to occur in close proximity, they are less likely to happen than single-crossover events.
05

Interference and the Frequency of Double-Crossover Events

Another reason for the reduced frequency of double-crossover events is a phenomenon known as interference. Interference is the effect by which the occurrence of a crossover event at one location along a chromosome reduces the probability of a second crossover event happening nearby. This is thought to ensure that genetic recombination occurs fairly evenly across the entire length of the chromosome, rather than being clustered in a small number of areas. In conclusion, double-crossover events occur less frequently than single-crossover events due to the relationship between gene positioning on a chromosome, the probability of crossover occurrence, and the effect of interference. These factors work together to ensure that genetic recombination promotes genetic diversity without clustering crossover events too closely together.

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Most popular questions from this chapter

List some of the differences between a linkage map obtained by analyzing crossovers and a physical map obtained by sequencing the DNA.

Why does more crossing over occur between two distantly linked genes than between two genes that are very close together on the same chromosome?

Assume that investigators crossed a strain of flies carrying the dominant eye mutation Lobe on the second chromosome with a strain homozygous for the second chromosome recessive mutations smooth abdomen and straw body. The \(\mathrm{F}_{1}\) Lobe females were then backcrossed with homozygous smooth abdomen, straw body males, and the following phenotypes were observed: (a) Give the gene order and map units between these three loci. (b) What is the coefficient of coincidence?

A female of genotype \\[ \frac{a}{+}+b^{c} \\] produces 100 meiotic tetrads. Of these, 68 show no crossover events. Of the remaining 32,20 show a crossover between \(a\) and \(b, 10\) show a crossover between \(b\) and \(c,\) and 2 show a double crossover between \(a\) and \(b\) and between \(b\) and \(c .\) Of the 400 gametes produced, how many of each of the 8 different genotypes will be produced? Assuming the order \(a-b-c\) and the allele arrangement previously shown, what is the map distance between these loci?

An organism of the genotype \(A a B b C c\) was testcrossed to a triply recessive organism (aabbcc). The genotypes of the progeny are presented in the following table. (a) If these three genes were all assorting independently, how many genotypic and phenotypic classes would result in the offspring, and in what proportion, assuming simple dominance and recessiveness in each gene pair? (b) Answer part (a) again, assuming the three genes are so tightly linked on a single chromosome that no crossover gametes were recovered in the sample of offspring. (c) What can you conclude from the actual data about the location of the three genes in relation to one another?

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