Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Inversions are said to "suppress crossing over." Is this terminology technically correct? If not, restate the description accurately.

Short Answer

Expert verified
Answer: Inversions can disrupt the process of crossing over by hindering the proper alignment of inverted regions in homologous chromosomes due to the change in gene orientation. This can potentially result in abnormal chromosomal products containing duplications and/or deletions, leading to reduced fertility or inviable offspring.

Step by step solution

01

Understanding Inversions

Inversions are a type of chromosomal mutation in which a segment of a chromosome is reversed. This means that the genes within the inverted segment change their orientation but remain on the same chromosome.
02

Understanding Crossing Over

Crossing over is the exchange of genetic material between homologous chromosomes during meiosis, which leads to the creation of new combinations of genes in the offspring. This process increases genetic diversity in the population.
03

Inversions and Crossing Over

When an inversion occurs in a chromosome, it can alter the process of crossing over. During meiosis, the inverted segment can't properly align with its homologous chromosome as their gene sequences now have different orientations. If crossing over does occur in the inverted region, it will result in the formation of aberrant chromosomes containing duplications and/or deletions, which may lead to reduced fertility or inviable offspring.
04

Restating the Description

The statement "inversions suppress crossing over" is not entirely accurate because inversions do not completely prevent crossing over from occurring. However, as discussed above, inversions can disrupt the normal process of crossing over in the affected region, leading to negative consequences. A more accurate description would be: "Inversions can disrupt the process of crossing over, potentially resulting in abnormal chromosomal products and reduced fertility or inviable offspring."

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

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

Genetic Diversity
Genetic diversity refers to the variety of genes within a species. It's like having a big, colorful box of crayons; each crayon is a unique gene variation. Higher genetic variability means a species can better adapt to changes and challenges in its environment, such as diseases or climate change.

How does genetic diversity come about? One key player is meiosis—the VIP process that mixes and matches genetic materials during the production of sperm and egg cells in sexually reproducing organisms. Chromosomal inversions, our tiny hiccups in DNA structure, may have a controversial role. While these inversions can sometimes protect a set of gene variations from being broken up, they can also muddle up genetic mixing by disrupting normal crossing over during meiosis. So, while inversions don't head straight to the genetic diversity party, they are busy at the entrance, deciding which genetic combos can make it onto the dance floor.
Meiosis
Meiosis is a special type of cell division used to create sperm and egg cells in organisms that reproduce sexually. It's like a genetic lottery where each ticket gets a random assortment of genes from mom and dad, leading to offspring that are genetically unique.

During meiosis, chromosomes are copied and shuffled to ensure that each sperm or egg gets one complete set of genes. This shuffling includes a step called crossing over, which is kind of like trading stickers between two collections to make sure no two packs are the same. The result is a fantastic mix of traits in the form of unique combinations of genes. This process is crucial for creating the genetic diversity we just talked about!
Crossing Over
Crossing over is a stellar matchmaker in genetics. It occurs during meiosis when the chromosomes cozy up and swap pieces of their DNA strands with each other. It's like two friends exchanging identical puzzle pieces, except these pieces carry genetic info.

When chromosomes cross over, they literally break and rejoin, creating new combinations of genes. This genetic reshuffling is like hitting the refresh button on genetic diversity. However, if a chromosomal inversion has RSVP'd to this exchange event, it can be like playing musical chairs with an uneven number of seats—it complicates the process, often leaving genes out of place or causing trouble when it's time for the chromosomes to separate.
Chromosomal Aberrations
Chromosomal aberrations are changes to the structure or number of chromosomes in cells. This can range from little quirks like an extra piece of chromosome, to major mess-ups like missing or extra chromosomes.

These changes can be caused by errors during cell division or damage from environmental factors like radiation. Aberrations can have a range of effects; some are harmless and might go unnoticed, while others can lead to serious health issues or even prevent an organism from reproducing. Chromosomal inversions are a specific type of aberration, which, as we've seen, can interfere with crossing over, putting a wrinkle in an otherwise smooth genetic fabric.
Chromosomal Mutations
Chromosomal mutations are the big edits in an organism's genetic script. Imagine proofreading your essay and instead of fixing typos, you end up changing whole paragraphs—that's what these mutations can be like.

They can be as simple as a small section of a chromosome flipping around (think chromosomal inversions), or as complex as large portions being deleted, duplicated, or moved elsewhere. Those mutations can have a range of impacts, from having no noticeable effect to causing significant changes in an organism's traits or health. Inversions in particular can play a tricky hand, sometimes leading to issues during meiosis and potentially playing a part in evolution by keeping certain groups of genes together.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

In this chapter, we have focused on chromosomal mutations resulting from a change in number or arrangement of chromosomes. In our discussions, 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 do we know that the extra chromosome causing Down syndrome is usually maternal in origin? (b) How do we know that human aneuploidy for each of the 22 autosomes occurs at conception, even though most often human aneuploids do not survive embryonic or fetal development and thus are never observed at birth? (c) How do we know that specific mutant phenotypes are due to changes in chromosome number or structure? (d) How do we know that the mutant Bar-eye phenotype in Drosophila is due to a duplicated gene region rather than to a change in the nucleotide sequence of a gene?

In a cross in Drosophila, a female heterozygous for the autosomally linked genes \(a, b, c, d,\) and \(e(a b c d e /+++++)\) was testcrossed with a male homozygous for all recessive alleles. Even though the distance between each of the loci was at least 3 map units, only four phenotypes were recovered, yielding the following data: Why are many expected crossover phenotypes missing? Can any of these loci be mapped from the data given here? If so, determine map distances.

Drosophila may be monosomic for chromosome \(4,\) yet remain fertile. Contrast the \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) results of the following crosses involving the recessive chromosome 4 trait, bent bristles: (a) monosomic IV, bent bristles \(\times\) diploid, normal bristles; (b) monosomic IV, normal bristles \(\times\) diploid, bent bristles.

Contrast the fertility of an allotetraploid with an autotriploid and an autotetraploid.

For a species with a diploid number of \(18,\) indicate how many chromosomes will be present in the somatic nuclei of individuals that are haploid, tetraploid, trisomic, and monosomic.

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free