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

Explain two ways that a chromosomal rearrangement can cause a position effect.

Short Answer

Expert verified
Two ways that a chromosomal rearrangement can cause a position effect are: 1) When a gene is relocated to a heterochromatic, or condensed, area of the chromosome leading to under-expression, and 2) The gene could move away from its necessary regulatory elements on the chromosome, leading to inappropriate expression levels. Both instances are caused by changes in the gene's physical location on the chromosome due to rearrangement.

Step by step solution

01

- Define Chromosomal Rearrangement

Chromosomal rearrangement refers to a structural alteration of a chromosome in which a part of a chromosome is shifted. There are four types of chromosomal rearrangements: inversions, deletions, duplications and translocations.
02

- Define Position Effect

The position effect refers to the change in the expression of a gene as a result of change in its location on a chromosome. Often, this change in position can cause a gene to be repressed or overexpressed.
03

- Explain first way chromosomal rearrangement can cause position effect

The first way chromosomal rearrangement might cause a position effect is through a relocation of a gene into an area of the chromosome that is heterochromatic, or condensed. These regions are less transcriptionally active, and as such, the gene could become expressed at lower levels than it would have otherwise if it were in a position conducive to transcription.
04

- Explain second way chromosomal rearrangement can cause position effect

The second way chromosomal rearrangement might cause a position effect is by moving a gene away from crucial regulatory elements on the chromosome. These elements help regulate the expression of the gene, and by being moved away from them, the gene could be expressed at inappropriate levels, or not at all. The fresh position of the gene places them under the control of new elements that may not be typically associated with their control.

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!

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 E coli, a methyltransferase encyme encoded by the dam gene recognizes the sequence \(5^{\prime}-\mathrm{GATC}-3\) and attaches a methyl group to the nitrogen at position 6 of adenine. E. coli strains that have the dam gene deleted are known to have a higher spontaneous mutation rate than normal strains. Explain why.

Trinucleotide repeat expansions (TNREs) are associated with seve eral different human inherited diseases. Certain types of TNREs produce a long stretch of the amino acid glutamine within the encoded protein. When a TNRE exerts its detrimental effect by producing a glutamane stretch, are the folloring statements true or false? A. The TNRE is within the coding sequence of the gene. B. The TNRE prevents RNA polymerase from transcribing the gene properly. \(C\). The trinucleotide sequence is CAG. D. The trinucleotide sequence is \(\mathrm{CCG}\).

Explain hor a mutagen can interfere with DNA replication to cause a mutation. Give two examples.

A segment of DNA has the folloving sequence: TTGGATGCTG AACCTACGAC A. What would the sequence be immediately after reaction with nitrous acid? Let the letters \(\mathrm{H}\) represent hypoxanthine and U represent uracil. B. Let's suppose this DNA was reacted with nitrous acid. The nitrous acid was then removed, and the DNA was replicated for two generations. What would be the sequences of the DNA products after the DNA had replicated tao times? (Note: Hypoxanthine pairs with cytasine.) Your answer should contain the secquences of four double helices.

What are the two main mechanisms by which cells repair doublestrand breaks? Briefly deseribe each one.

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