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

Short Answer

Expert verified
The higher rate of crossing over between two distantly linked genes compared to two genes that are close together on the same chromosome is due to the increased likelihood of a crossover event occurring between them. Since crossing over is a random process, the greater the distance between the genes, the higher the probability of a crossover happening within that region. This results in more crossing over between distantly linked genes, leading to greater genetic diversity in the offspring.

Step by step solution

01

Understand the basics of meiosis and crossing over

During meiosis, the process that creates gametes (sperm and egg cells), chromosomes are exchanged between homologous chromosomes (chromosomes that are similar in structure). This exchange, called crossing over, leads to the recombination of genetic material, ensuring greater genetic diversity in the offspring. Crossing over happens during the prophase of meiosis I.
02

Explain linked genes and recombination frequency

Genes located on the same chromosome are considered linked, meaning they are inherited together during the formation of gametes. However, the extent to which they are linked depends on the distance between them. Recombination frequency (the likelihood of a crossover event occurring between two genes) is directly related to the distance between those genes.
03

Describe the effect of distance on crossing over

The further apart two genes are on a chromosome, the more likely it is that a crossover event will occur between them. Crossing over is a random process, so the longer the segment between genes, the higher the probability of a crossover happening within that region. Consequently, more crossing over occurs between distantly linked genes compared to genes that are close together on the same chromosome.
04

Illustrate the concept with an example

For example, consider two genes A and B located on the same chromosome. If they are very close together, the chance of a crossover event happening between them is low because there is a small region for this event to take place. However, if the genes are further apart on the chromosome, the larger region increases the likelihood of a crossover event occurring between them.
05

Summarize the main points

In conclusion, more crossing over occurs between distantly linked genes compared to closely linked genes because the likelihood of a crossover event taking place is directly related to the distance between genes on a chromosome. The greater the distance between the genes, the higher the chance of crossing over during meiosis, ensuring greater genetic diversity in the offspring.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Meiosis
At its core, meiosis is a specialized form of cell division responsible for producing gametes, sperm in males, and eggs in females. Unlike regular cell division, or mitosis, where a single cell divides to produce two identical daughter cells, meiosis results in four unique daughter cells, each with half the number of chromosomes of the parent cell.

This reduction is crucial for sexual reproduction because it ensures that when two gametes unite during fertilization, the resulting offspring has the species-specific number of chromosomes. Meiosis consists of two rounds of division: meiosis I and meiosis II. The critical event distinguishing meiosis I from mitosis is crossing over during prophase I, where homologous chromosomes exchange genetic material to create new genetic combinations. This process not only contributes to the uniqueness of each gamete but also increases the genetic diversity of the offspring.
Recombination Frequency
Understanding recombination frequency helps geneticists predict how genes will be passed on to the next generation. This concept, defined as the probability of a crossover between two specific genes, is intrinsically linked to the physical location of these genes on a chromosome.

When genes are close to each other, they are considered linked and tend to be inherited together; crossovers between them are less frequent. In contrast, genes that are farther apart have a higher recombination frequency, meaning crossovers occur more often, leading to genetic combinations that differ from the parent. Because recombination frequency is proportional to the distance between genes, it can be measured and used in constructing genetic maps, essentially providing a rough estimate of where genes are located on chromosomes based on how often they recombine.
Linked Genes
When we talk about linked genes, we are referring to genes that reside close together on the same chromosome and thus are usually inherited as a unit. This physical proximity means that the alleles, or different versions, of these genes are less likely to be separated by crossing over during meiosis.

The term 'linkage' describes this tendency to be inherited together, and the strength of the linkage depends on how close these genes are. However, it's important to note that no genes are absolutely linked; with a long enough chromosome or sufficient distance between genes, a crossover is always possible, although it might be rare. This concept of linkage has significant implications in understanding how traits are passed down and can influence patterns of inheritance observed in genetic crosses and pedigrees.
Genetic Diversity
The genetic diversity found within and among populations is largely a result of processes like meiosis and the crossing over it entails. This genetic variability is fundamental to the survival and adaptability of species. During meiosis, especially in the prophase of the first division, chromosomes reciprocally exchange segments in crossing over events.

These events shuffle alleles between chromosomes, leading to new genetic combinations within gametes. The more diverse the genetic combinations, the greater the ability of a population to withstand environmental changes and pressures, such as diseases or climate change. Therefore, a higher frequency of crossing over, which is more probable between distantly linked genes, can contribute significantly to the genetic diversity and resilience of organisms.

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Most popular questions from this chapter

Review the Chapter Concepts list on page 94. 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.

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

A female of genotype \[ \frac{a}{+}+\frac{b}{+}+ \] 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 abc and the allele arrangement previously shown, what is the map distance between these loci?

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? (e) When designed matings cannot be conducted in an organism (for example, in humans), how do we learn that genes are linked, and how do we map them?

Another cross in Drosophila involved the recessive, X-linked genes yellow (y), white (w), and cut (ct). 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 F1 females were wild type for all three traits, while the F1 males expressed the yellow-body and white-eye traits. The cross was carried to an F2 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 F1 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 F2 female offspring be used to construct the map? Why or why not?

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