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 during meiosis due to a combination of factors such as probability, crossover interference, and constraints of the recombination machinery. Two separate crossover events need to occur close to each other on the same pair of homologous chromosomes, making double-crossovers less likely by random chance. Additionally, the occurrence of one crossover event reduces the likelihood of another crossover event happening nearby due to interference. Lastly, the molecular machinery responsible for homologous recombination may have constraints that make double-crossover events less energetically favorable or more challenging to complete.

Step by step solution

01

Definition of Crossover Events and Homologous Recombination

Crossover events occur during the process of meiosis, which is the type of cell division that produces gametes (sperm and egg cells) in sexually reproducing organisms. In a crossover event, homologous chromosomes (i.e., chromosomes that have the same genes but may carry different alleles) exchange genetic material through a process called homologous recombination.
02

Single-Crossover Events

In a single-crossover event, homologous chromosomes exchange genetic material only once, resulting in two non-sister chromatids swapping parts of their DNA. This leads to a recombinant chromosome with a unique combination of alleles, increasing genetic diversity among offspring.
03

Double-Crossover Events

In a double-crossover event, two separate crossover events occur between the same two homologous chromosomes during meiosis. This means that genetic material is first exchanged, and then a second exchange occurs, essentially "undoing" the first crossover.
04

Factors Influencing Crossover Frequency

The frequency of crossover events is influenced by factors such as chromosome size, the presence of crossover hotspots (regions with higher recombination rates), and the degree of physical contact between homologous chromosomes during meiosis.
05

Reasons for Lesser Frequency of Double-Crossover Events

Double-crossover events are expected to be less frequent than single-crossover events for the following reasons: 1. Probability: Two separate crossover events need to occur close to each other on the same pair of homologous chromosomes, meaning that double-crossovers are less likely simply due to random chance. 2. Interference: Crossover interference is a phenomenon in which the occurrence of one crossover event reduces the likelihood of another crossover event happening nearby on the same pair of homologous chromosomes. This means that if a single-crossover event occurs, it suppresses the formation of a double-crossover event in the vicinity. 3. Recombination machinery: The molecular machinery responsible for homologous recombination may have constraints that make double-crossover events less energetically favorable or more challenging to complete, further reducing their likelihood. In conclusion, double-crossover events are expected to be less frequent than single-crossover events due to a combination of probabilistic factors, interference between nearby crossovers, and the constraints of the recombination machinery involved in the process.

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DNA markers have greatly enhanced the mapping of genes in humans. What are DNA markers, and what advantage do they confer?

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In Drosophila, Dichaete ( \(D\) ) is a mutation on chromosome III with a dominant effect on wing shape. It is lethal when homozygous. The genes \(e\)bony body \((e)\) and pink eye (p) are recessive mutations on chromosome III. Flies from a Dichaete stock were crossed to homozygous ebony, pink flies, and the \(\mathrm{F}_{1}\) progeny with a Dichaete phenotype were backcrossed to the ebony, pink homozygotes. (a) Using the results of this backcross shown in the following table, diagram the cross, showing the genotypes of the parents and offspring of both crosses. (b) What is the sequence and interlocus distance between these three genes?

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