Chapter 13: Problem 9
The probability of a crossover occurring between two genes on the same chromosome _____. a. is unrelated to the distance between them b. decreases with the distance between them c. increases with the distance between them
Short Answer
Expert verified
c. Increases with the distance between them.
Step by step solution
01
Understanding Genetic Recombination
Genetic recombination refers to the exchange of genetic material between homologous chromosomes during meiosis, a process critical for generating genetic diversity in offspring.
02
Analyzing Crossover Events
A crossover event occurs when two homologous chromosomes exchange segments. The likelihood of this event happening between two genes on a chromosome is not random; it depends on the distance between them.
03
Relation between Gene Distance and Crossover Probability
The further apart two genes are on a chromosome, the more likely it is that a crossover occurs between them. This is because there is more physical space for crossover events to occur.
04
Evaluating the Answer Choices
Choice a is incorrect because the probability of crossover is related to the distance between the genes. Choice b is incorrect because as the distance increases, the probability also increases, not decreases. Choice c correctly states that crossover likelihood increases with distance.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Crossover Events
Crossover events are a fascinating aspect of genetic recombination that occur during meiosis, the process where cells divide to form gametes (sperm and egg cells). During meiosis, homologous chromosomes—pairs of chromosomes of the same type—align with each other and can physically exchange segments of DNA. This "swapping" of genetic material is what we refer to as a crossover event.
A crossover event contributes to genetic diversity by reordering alleles, the versions of a gene present on a chromosome, creating new combinations of alleles in the offspring. Genetic variation increases the likelihood of beneficial traits being passed on and enhances a population's ability to adapt to changing environments.
Understanding crossover events is crucial since they underpin the genetic variation seen in most sexually reproducing organisms. They ensure that no two gametes are genetically identical, adding a considerable degree of unpredictability to genetic inheritance.
A crossover event contributes to genetic diversity by reordering alleles, the versions of a gene present on a chromosome, creating new combinations of alleles in the offspring. Genetic variation increases the likelihood of beneficial traits being passed on and enhances a population's ability to adapt to changing environments.
Understanding crossover events is crucial since they underpin the genetic variation seen in most sexually reproducing organisms. They ensure that no two gametes are genetically identical, adding a considerable degree of unpredictability to genetic inheritance.
Gene Distance
The concept of gene distance is pivotal when considering crossover events. Gene distance refers to the physical space between two genes on a chromosome. Importantly, this distance can influence the likelihood that a crossover event will occur between them.
The basic principle is quite intuitive: the further apart two genes are on the same chromosome, the higher the probability of a crossover. This happens because more physical space between genes provides more opportunity for enzyme-mediated breaks and exchanges in the DNA strands.
The basic principle is quite intuitive: the further apart two genes are on the same chromosome, the higher the probability of a crossover. This happens because more physical space between genes provides more opportunity for enzyme-mediated breaks and exchanges in the DNA strands.
- If two genes are very close to each other, a crossover between them is less likely simply due to a lack of space for the physical exchange to occur.
- Conversely, genes situated far apart on the chromosome are more exposed to the mechanisms facilitating crossover, thus increasing the chance of recombination event.
Meiosis
Meiosis is a special type of cell division that reduces the number of chromosomes in parent cells by half, producing four gametes. This process is essential for sexual reproduction in eukaryotic organisms. Meiosis consists of two successive divisions, meiosis I and meiosis II, and undergoes several stages: prophase, metaphase, anaphase, and telophase. Each has specific and vital functions.
One of the most critical aspects of meiosis is that it introduces genetic variation through crossover events. During prophase I, homologous chromosomes pair up closely in a process termed synapsis. This proximity allows for segments of DNA to be swapped, leading to new allele combinations.
One of the most critical aspects of meiosis is that it introduces genetic variation through crossover events. During prophase I, homologous chromosomes pair up closely in a process termed synapsis. This proximity allows for segments of DNA to be swapped, leading to new allele combinations.
- Meiosis not only halves the chromosome number but also enhances genetic diversity.
- The end result is gametes that are all genetically distinct, a crucial factor for evolution and adaptation in populations.
Chromosome
A chromosome is a thread-like structure located within the nucleus of cells, composed of a single molecule of DNA and associated proteins. Chromosomes carry the cell's genetic information and play a fundamental role during cell division.
In each species, a characteristic number of chromosomes is found. For example, humans have 23 pairs of chromosomes, totaling 46 per cell. During cell division, chromosomes ensure that DNA is accurately replicated and distributed to new cells.
In each species, a characteristic number of chromosomes is found. For example, humans have 23 pairs of chromosomes, totaling 46 per cell. During cell division, chromosomes ensure that DNA is accurately replicated and distributed to new cells.
- Chromosomes are involved in maintaining the integrity of the genetic information too, ensuring each daughter cell receives a complete set.
- Alterations or errors in chromosomes can lead to genetic disorders or variations, affecting an organism's health or development.