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

Contrast the structure of SINE and LINE DNA sequences. Why are LINEs referred to as retrotransposons?

Short Answer

Expert verified
Answer: LINEs are called retrotransposons because they transpose via an RNA intermediate using reverse transcription, similar to the mechanism used by retroviruses and other retrotransposons. LINEs have a longer DNA sequence (over 1,000 base pairs) and possess two open reading frames (ORFs) that code for proteins needed for their own transposition. In contrast, SINEs are shorter (80-500 base pairs) and non-coding, and they are derived from small RNA genes like tRNAs or 7SL RNA.

Step by step solution

01

Understand SINEs and LINEs

SINEs (Short Interspersed Nuclear Elements) and LINEs (Long Interspersed Nuclear Elements) are types of repetitive DNA sequences found in the genome. They belong to the class of transposable elements, which can move to new positions within the genome. Let's first describe their structures briefly: SINEs: They are shorter DNA sequences (80-500 base pairs long) that are non-coding (do not code for proteins) and are usually derived from small RNA genes like tRNAs or 7SL RNA. LINEs: They are longer DNA sequences (over 1,000 base pairs long) that can code for proteins needed for their own transposition. They typically contain two open reading frames (ORFs), which code for the proteins required for their own mobilization. Now, let's contrast the structure of SINE and LINE DNA sequences.
02

Contrasting Structures of SINEs and LINEs

1. Length: SINEs are shorter (80-500 base pairs) compared to LINEs (over 1,000 base pairs). 2. Protein-coding capacity: SINEs are non-coding, while LINEs have ORFs that code for proteins needed for their own transposition. 3. Origin: SINEs are derived from small RNA genes like tRNAs or 7SL RNA, while LINEs are not derived from these sources.
03

Retrotransposons: Definition and Connection to LINEs

Retrotransposons are transposable elements that are transposed via an RNA intermediate. They use reverse transcription (conversion of RNA into DNA), followed by integration of the copied DNA into a new genomic location. This process requires the action of a reverse transcriptase enzyme, which is coded by the retrotransposon itself. LINEs are referred to as retrotransposons because they use a similar mechanism for their transposition: 1. Transcription: LINEs are transcribed into RNA by cellular machinery. 2. Translation: The RNA transcript is translated into proteins, including a reverse transcriptase enzyme, by the cell's ribosomes. 3. Reverse transcription: The RNA transcript serves as a template for reverse transcriptase to synthesize a complementary DNA (cDNA) copy of the LINE sequence. 4. Integration: The cDNA is integrated into a new genomic location by the action of the LINE-encoded endonuclease enzyme. In summary, LINEs are referred to as retrotransposons because they transpose via an RNA intermediate using reverse transcription, akin to the mechanism used by retroviruses and other retrotransposons.

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

Why might we predict that the organization of eukaryotic genetic material will be more complex than that of viruses or bacteria?

The human genome contains approximately \(10^{6}\) copies of an \(A l u\) sequence, one of the best-studied classes of short interspersed elements (SINEs), per haploid genome. Individual Alus share a 282 -nucleotide consensus sequence followed by a 3 '-adeninerich tail region. Given that there are approximately \(3 \times 10^{9}\) bp per human haploid genome, about how many base pairs are spaced between each Alu sequence?

Contrast the various categories of repetitive DNA.

In this chapter, we focused on how DNA is organized at the chromosomal level. Along the way, 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, propose answers to the following fundamental questions: (a) How do we know that viral and bacterial chromosomes most often consist of circular DNA molecules devoid of protein? (b) What is the experimental basis for concluding that puffs in polytene chromosomes and loops in lampbrush chromosomes are areas of intense transcription of RNA? (c) How did we learn that eukaryotic chromatin exists in the form of repeating nucleosomes, each consisting of about 200 base pairs and an octamer of histones? (d) How do we know that satellite DNA consists of repetitive sequences and has been derived from regions of the centromere?

Define satellite DNA. Describe where it is found in the genome of eukaryotes and its role as part of chromosomes.

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