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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 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

Colored aleurone in the kernels of corn is due to the dominant allele \(R\). The recessive allele \(r,\) when homozygous, produces colorless aleurone. The plant color (not the kernel color) is controlled by another gene with two alleles, \(Y\) and \(y\). The dominant \(Y\) allele results in green color, whereas the homozygous presence of the recessive \(y\) allele causes the plant to appear yellow. In a testcross between a plant of unknown genotype and phenotype and a plant that is homozygous recessive for both traits, the following progeny were obtained: $$\begin{array}{lc} \text { colored, green } & 88 \\ \text { colored, yellow } & 12 \\ \text { colorless, green } & 8 \\ \text { colorless, yellow } & 92 \end{array}$$ Explain how these results were obtained by determining the exact genotype and phenotype of the unknown plant, including the precise arrangement of the alleles on the homologs.

In Drosophila, a female fly is heterozygous for three mutations, Bar eyes \((B),\) miniature wings \((m),\) and ebony body \((e)\) Note that Bar is a dominant mutation. The fly is crossed to a male with normal eyes, miniature wings, and ebony body. The results of the cross are as follows. Interpret the results of this cross. If you conclude that linkage is involved between any of the genes, determine the map distance(s) between them.

Three loci, mitochondrial malate dehydrogenase that forms \(a\) and \(b(M D H a, M D H b),\) glucouronidase that forms 1 and 2 \((G U S 1, G U S 2),\) and a histone gene that forms \(+\) and \(-\left(H^{+},\right.\) \(\left.H^{-}\right),\) are located on chromosome \(\\# 7\) in humans. Assume that the \(M D H\) locus is at position \(35, G U S\) at position \(45,\) and \(H\) at position \(75 .\) A female whose mother was homozygous for \(M D H a, G U S 2,\) and \(H^{+}\) and whose father was homozygous for \(M D H b, G U S 1,\) and \(H^{-}\) produces a sample of 1000 egg cells. Give the genotypes and expected numbers of the various types of cells she would produce. Assume no chromosomal interference.

Review the Chapter Concepts list on page \(138 .\) Most of these center around 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.

Another cross in Drosophila involved the recessive, X-linked genes yellow \((y),\) white \((w),\) and \(c u t(c t) .\) A yellow-bodied, white-eyed female with normal wings was crossed to a male whose eyes and body were normal but whose wings were cut. The \(\mathrm{F}_{1}\) females were wild type for all three traits, while the \(\mathrm{F}_{1}\) males expressed the yellow-body and white- eye traits. The cross was carried to an \(\mathrm{F}_{2}\) progeny, and only male offspring were tallied. On the basis of the data shown here, a genetic map was constructed. (a) Diagram the genotypes of the \(\mathrm{F}_{1}\) parents. (b) Construct a map, assuming that white is at locus 1.5 on the X chromosome. (c) Were any double-crossover offspring expected? (d) Could the \(\mathrm{F}_{2}\) female offspring be used to construct the map? Why or why not?

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