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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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Most popular questions from this chapter

Drosophila females homozygous for the third chromosomal genes pink eye (p) and ebony body (e) were crossed with males homozygous for the second chromosomal gene dumpy wings (dp). Because these genes are recessive, all offspring were wild type (normal). \(F_{1}\) females were testcrossed to triply recessive males. If we assume that the two linked genes ( \(p\) and \(e\) ) are 20 mu apart, predict the results of this cross. If the reciprocal cross were made (F1 males-where no crossing over occurs-with triply recessive females), how would the results vary, if at all?

Review the Chapter Concepts list on p. \(121 .\) Most of these center on the process of crossing over between linked genes. Write a short essay that discusses how crossing over can be detected and how the resultant data provide the basis of chromosome mapping.

In Drosophila, a cross was made between females expressing the three X-linked recessive traits, scute bristles \((s c),\) sable body \((s)\) and vermilion eyes ( \(v\) ), and wild-type males. All females were wild type in the \(F_{1},\) while all males expressed all three mutant traits. The cross was carried to the \(\mathrm{F}_{2}\) generation and 1000 offspring were counted, with the results shown in the following table. No determination of sex was made in the \(\mathrm{F}_{2}\) data. (a) Using proper nomenclature, determine the genotypes of the \(P_{1}\) and \(F_{1}\) parents. (b) Determine the sequence of the three genes and the map distance between them. (c) Are there more or fewer double crossovers than expected? (d) Calculate the coefficient of coincidence; does this represent positive or negative interference?

In this chapter, we focused on linkage, chromosomal mapping, and many associated phenomena. In the process, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions? (a) How was it established experimentally that the frequency of recombination (crossing over) between two genes is related to the distance between them along the chromosome? (b) How do we know that specific genes are linked on a single chromosome, in contrast to being located on separate chromosomes? (c) How do we know that crossing over results from a physical exchange between chromatids? (d) How do we know that sister chromatids undergo recombination during mitosis?

What three essential criteria must be met in order to execute a successful mapping cross?

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