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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

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Answer: The distance between genes on a chromosome affects the frequency of crossing over during meiosis because the likelihood of chiasmata formation increases with the distance between the genes. The farther apart two genes are, the more likely a chiasma will form between them, leading to a higher frequency of crossing over and greater genetic diversity in offspring. Conversely, when genes are positioned close together, they are less likely to undergo crossing over and may be inherited together as a group, known as genetic linkage.

Step by step solution

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1. Understanding Crossing Over and Meiosis

Crossing over is an important process that occurs during meiosis, a type of cell division responsible for the production of gametes (sperm and egg cells). During meiosis, homologous chromosomes exchange genetic material through a process called recombination, which can result in new combinations of genes in the offspring. This is a significant source of genetic diversity.
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2. The role of Chiasmata in Crossing Over

During the first stage of meiosis, known as prophase I, homologous chromosomes pair up and form structures called chiasmata, where genetic material is exchanged between the chromosomes. The frequency of chiasmata formation can vary depending on the total length of the chromosome and the distance between genes of interest.
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3. Recombination Frequency and Gene Distance

The recombination frequency between two genes on a chromosome is proportional to the distance between those genes. The farther apart two genes are, the more likely a chiasma will form between them, leading to a higher frequency of crossing over. This relationship is often expressed using a unit called a centimorgan (cM), which represents the relative distance between genes.
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4. The Impact of Gene Distance on Crossing Over

Since crossing over happens more frequently between distantly linked genes, we observe more recombination events for genes located further apart on the chromosome. This increased recombination can result in a greater variety of genetic combinations in offspring, giving them a greater chance of survival and adaptation to changing environments. Conversely, when genes are positioned close together on a chromosome, they are less likely to undergo crossing over and may be inherited together as a group, known as genetic linkage.
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5. Conclusion

In summary, more crossing over occurs between distantly linked genes because the likelihood of chiasmata formation increases with the distance between the genes. This increased recombination frequency ensures genetic diversity and adaptation in offspring.

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Key Concepts

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

Crossing Over
Crossing over is a fascinating process that occurs during meiosis, a crucial type of cell division that leads to the production of gametes like sperm and egg cells. During meiosis, homologous chromosomes pair up closely, allowing them to exchange segments of genetic material. This exchange is what we call "crossing over." As a result, new combinations of genes can be created, changing the genetic makeup of the resulting cells.

This is not only important because it contributes to genetic variation among offspring, but it also plays a role in evolution. By mixing up genetic material, crossing over helps species adapt to changing environments, ultimately contributing to greater biodiversity.
Meiosis
Meiosis is a special type of cell division distinct from mitosis. It reduces the chromosome number by half, resulting in the formation of four genetically diverse gametes from one original cell. This division includes two main stages, meiosis I and meiosis II. Each of these stages has several phases like prophase, metaphase, anaphase, and telophase, similar to mitosis.

However, meiosis has unique features that mitosis does not, such as crossing over during prophase I, where homologous chromosomes exchange genetic material. This exchange results in recombinant chromosomes that hold a shuffled arrangement of genes. Meiosis is essential for sexual reproduction because it ensures that offspring receive the correct number of chromosomes.
Gene Linkage
Gene linkage refers to the tendency of genes that are located close to each other on the same chromosome to be inherited together during meiosis. Such genes do not assort independently, as Mendel's law of independent assortment would suggest. Because they are physically close on the chromosome, they usually do not get shuffled independently during crossing over.

As a result, gene linkage can influence trait inheritance, sometimes making it hard to distinguish between closely linked genes. When genes are closely linked, they tend to be co-inherited, potentially affecting whether certain traits appear together more frequently in offspring.
Recombination Frequency
Recombination frequency is a measure of the likelihood that crossing over will occur between two genes during meiosis. It's directly related to the distance between genes on a chromosome. The farther apart the genes are, the higher the recombination frequency.

Recombination frequency is usually measured in centimorgans (cM). One centimorgan corresponds to a 1% chance that a crossover will occur between two genes per generation. This concept is a key tool for geneticists when creating gene maps, which are diagrams showing the relative positions of genes on a chromosome. Understanding recombination frequency aids in studying genetic linkage and mapping genetic traits.

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Most popular questions from this chapter

Phenotypically wild F1 female Drosophila, whose mothers had light eyes (It) and fathers had straw (stw) bristles, produced the following offspring when crossed with homozygous light-straw males: Phenotype  Number  light-straw 22 wild 18 light 990 straw 9702000 Compute the map distance between the light and straw loci.

Describe the cytological observation that suggests that crossing over occurs during the first meiotic prophase.

In the fruit fly, Drosophila melanogaster, a spineless (no wing bristles) female fly is mated to a male that is claret (dark eyes) and hairless (no thoracic bristles). Phenotypically wild-type F1 female progeny were mated to fully homozygous (mutant) males, and the following progeny ( 1000 total) were observed:  Phenotypes  Number Observed  spineless 321 wild 38 claret, spineless 130 claret 18 claret, hairless 309 hairless, claret, spineless 32 hairless 140 hairless, spineless 12 (a) Which gene is in the middle? (b) With respect to the three genes mentioned in the problem, what are the genotypes of the homozygous parents used in making the phenotypically wild F1 heterozygote? (c) What are the map distances between the three genes? A correct formula with the values "plugged in" for each distance will be sufficient. (d) What is the coefficient of coincidence? A correct formula with the values "plugged in" will be sufficient.

A backcross was set up between two homozygous laboratory mouse strains A and B, with the F1 backcrossed to B. The F2 were typed using SNPs x and y, which varied between strains A and B(xA,xB,yA,yB). Out of 100 mice, 38 were xAyA,40 were xByB 11 were xAyB, and 11 were xByA. What is the genetic distance between SNPs x and y?

Why is a 50 percent recovery of single-crossover products the upper limit, even when crossing over always occurs between two linked genes?

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