Chapter 6: Problem 10
Inversions are said to "suppress crossing over." Is this ter. minology technically correct? If not, restate the description accurately.
Short Answer
Expert verified
Answer: Inversions can reduce or prevent crossing over in the affected chromosomal regions.
Step by step solution
01
Understanding Inversions
Inversions are chromosomal mutations in which a segment of a chromosome is reversed end to end. An inversion occurs when a chromosome breaks in two places and the resulting piece of the chromosome is reinserted in the opposite orientation.
02
Understanding Crossing Over
Crossing over is a process that occurs during meiosis, where homologous chromosomes (two chromosomes having the same genes at the same loci but can have different alleles) exchange segments by breaking and rejoining each other. It results in a recombinant chromosome with a different combination of alleles than the parent chromosomes. Crossing over increases genetic diversity within a population.
03
The Impact of Inversions on Crossing Over
When an inversion occurs in one of the homologous chromosomes, the corresponding segments may not align properly during meiosis. As a result, the exchange of genetic material through crossover becomes difficult, if not impossible, because the break points required for exchange do not match. In other words, the inversion suppresses crossing over.
04
Evaluating the Terminology
While the term "Inversions suppress crossing over" is generally understandable, it may not be technically precise. A more accurate description could be: "Inversions can reduce or prevent crossing over in the affected chromosomal regions."
This description acknowledges that inversions can have varying degrees of impact on crossing over, rather than suggesting that they always completely suppress it. Additionally, it clarifies that the suppression of crossing over is specific to the affected regions of chromosomes and not a complete suppression across all regions.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Chromosomal Inversions
Chromosomal inversions are fascinating genetic phenomena where a part of a chromosome breaks off, flips around, and then reinserts itself backwards into the original chromosome. Imagine a section of a chromosome akin to a string of beads, and someone flips a section of this string before placing it back. This creates an inversion. There are two main types:
- Paracentric inversions: These do not involve the centromere, occurring in one arm of the chromosome.
- Pericentric inversions: These include the centromere, involving both arms of the chromosome.
Crossing Over
Crossing over is a critical genetic process that occurs during meiosis, which is a type of cell division that reduces the chromosome number by half. During meiosis, homologous chromosomes—chromosomes with the same sequence of genes—pair up. At this point, crossing over can happen. Each chromosome can swap sections with its homologous partner, effectively creating new combinations of genes.
This gene shuffling is a key contributor to genetic diversity, which can improve a population’s adaptability to changing environments and is essential for evolution. However, crossing over isn’t always perfect. For example, if a chromosomal inversion is present, the standard alignment of homologous chromosomes is disrupted. This means crossing over might not proceed smoothly, potentially reducing the overall genetic shuffling in areas where inversions occur.
This gene shuffling is a key contributor to genetic diversity, which can improve a population’s adaptability to changing environments and is essential for evolution. However, crossing over isn’t always perfect. For example, if a chromosomal inversion is present, the standard alignment of homologous chromosomes is disrupted. This means crossing over might not proceed smoothly, potentially reducing the overall genetic shuffling in areas where inversions occur.
Meiosis
Meiosis is a specialized form of cell division that is essential for sexual reproduction. It consists of two successive divisions, meiosis I and meiosis II, each with its own phases. These divisions result in four genetically distinct daughter cells, each containing half the number of chromosomes as the original cell.
- In meiosis I, homologous chromosomes separate.
- In meiosis II, sister chromatids split apart.