Related Experiment Video
Updated: Nov 18, 2025

07:28
Identification of Functionally-Relevant Lentivirus Integration Sites in an Insertional Mutagenesis Cell Library
Published on: January 10, 2025
524
TEfinder: A Bioinformatics Pipeline for Detecting New Transposable Element Insertion Events in Next-Generation
Vista Sohrab1, Cristina López-Díaz2, Antonio Di Pietro2
1Department of Biochemistry and Molecular Biology, University of Massachusetts Amherst, Amherst, MA 01003, USA.
Genes
|February 9, 2021
Summary
Transposable elements (TEs) are mobile genetic sequences. TEfinder is a new bioinformatics tool that simplifies the detection of new TE insertions, aiding genome evolution studies.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- Transposable elements (TEs) are mobile genetic sequences driving genome evolution and genetic instability.
- Existing bioinformatics tools for TE insertion detection often have limitations like narrow focus or complex dependencies.
- Accurate identification of TEs is crucial for understanding their role in biological processes.
Purpose of the Study:
- To develop a user-friendly bioinformatics pipeline for detecting new transposable element insertions.
- To minimize software and input file dependencies for broader accessibility.
- To provide a practical tool for analyzing TE dynamics in evolving populations.
Main Methods:
- Developed TEfinder, a pipeline requiring minimal external software (BEDTools, SAMtools, Picard).
- Input requirements include reference genome (FASTA), paired-end read alignment (BAM/SAM), existing TEs (GTF), and TE names (TXT).
- Tested TEfinder on evolving populations of *Fusarium oxysporum* from a short-term adaptation study.
Main Results:
- TEfinder effectively detected new transposable element insertion events.
- The tool demonstrated ease of use and practicality in analyzing TE insertions.
- Successful application in identifying TE dynamics within experimental populations.
Conclusions:
- TEfinder offers a simplified and accessible approach to detecting transposable element insertions.
- The pipeline's minimal dependencies make it a practical choice for researchers.
- This tool facilitates the study of genome evolution and genetic variation driven by TEs.
Keywords:
genome evolutionmobile element insertion eventsnext-generation sequencing (NGS)transposable elementsMore Related Videos
Related Concept Videos
Overview of Transposition and Recombination
18.0K
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...
18.0K
DNA-only Transposons
15.8K
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...
15.8K
Transposons
627
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...
627
Non-LTR Retrotransposons
12.6K
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...
12.6K
LTR Retrotransposons
18.8K
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...
18.8K
piRNA - Piwi-interacting RNAs
7.2K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
7.2K

