Related Experiment Video
Updated: Jul 4, 2026

04:04
Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity
Published on: January 20, 2023
The distribution and conservation of retrotransposable elements in cattle
1Department of Dairy Science, University of Wisconsin, Madison, Wisconsin 53706, USA. hkhatib@wisc.edu
Epigenetics
|June 10, 2008
Summary
Retrotransposable elements like SINEs and LINEs show distinct distribution patterns in imprinted genes versus X-linked and olfactory genes. This suggests different regulatory mechanisms control genomic imprinting and X inactivation.
Area of Science:
- Genomics
- Molecular Biology
- Comparative Genomics
Background:
- Retrotransposable elements (RTEs) are mobile genetic sequences.
- Monoallelically-expressed genes, including imprinted, X-linked, and olfactory genes, exhibit unique expression patterns.
- Understanding RTE distribution is crucial for deciphering gene regulation.
Purpose of the Study:
- To investigate the distribution of RTEs in monoallelically-expressed genes versus biallelically-expressed genes.
- To analyze the conservation of RTEs in imprinted and homeobox genes across human, mouse, and cattle.
- To compare RTE frequencies in imprinted genes with X-linked and olfactory genes.
Main Methods:
- Comparative analysis of RTE distribution (SINEs and LINEs) in gene sets.
- Examination of imprinted, X-linked, olfactory, and homeobox genes.
- Cross-species comparison (human, mouse, cattle).
Main Results:
- Short interspersed nuclear elements (SINEs) were significantly less frequent in imprinted genes compared to nonimprinted genes in cattle.
- Long interspersed nuclear elements (LINEs) were enriched on the bovine X chromosome compared to autosomes.
- High densities of LINE-1s were observed in bovine and mouse olfactory genes compared to imprinted genes.
Conclusions:
- The lower density of SINEs and LINEs in imprinted genes compared to the X chromosome suggests distinct regulatory mechanisms for genomic imprinting and X inactivation.
- RTE distribution varies significantly across different classes of monoallelically-expressed genes.
- Conservation analysis of RTEs in imprinted and homeobox genes provides insights into evolutionary regulatory strategies.
Related Concept Videos
Overview of Transposition and Recombination
Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
LTR Retrotransposons
LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
Non-LTR Retrotransposons
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
DNA-only Transposons
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
The donor site from where the transposon is excised is either degraded or...
Retroviruses
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
Transposons
Transposons, or "jumping genes," are small mobile genetic elements (MGEs) that range from 700 to 40,000 base pairs in length. They are found in all organisms and can move within the same chromosome or transfer to different chromosomes. In some cases, transposons can also jump between different host DNA molecules, such as plasmids or viruses, contributing to genetic variability.Barbara McClintock first discovered these mobile genetic elements in the 1940s while studying maize genetics, and she...

