Exploring the Relationship of Transposable Elements and Ageing: Causes and Consequences.
Miriam Merenciano1, Anaïs Larue1,2, Chloé Garambois1
1Laboratoire de Biométrie et Biologie Evolutive, CNRS, UMR5558, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.
Genome Biology and Evolution
|May 15, 2025
Summary
Transposable elements (TEs) can cause ageing by disrupting cellular functions as epigenetic silencing weakens with age. This review examines the complex, dual role of TEs in the ageing process.
Area of Science:
- Genetics
- Molecular Biology
- Gerontology
Background:
- Ageing is a natural process involving physiological decline and increased disease risk.
- Transposable elements (TEs) are mobile DNA sequences that can cause mutations and alter cellular functions.
- Epigenetic mechanisms normally suppress TEs, but these fail with age.
Purpose of the Study:
- To explore the dual role of transposable elements (TEs) in the ageing process.
- To review how TE activity contributes to age-related decline.
- To discuss the complex relationship between TEs and ageing.
Main Methods:
- Literature review of studies on transposable elements and ageing.
- Analysis of epigenetic regulation of TEs.
- Examination of TE-induced genomic alterations.
Main Results:
- TEs contribute to ageing by increasing genomic instability and disrupting gene expression.
- Epigenetic silencing of TEs diminishes with advancing age.
- Increased TE activity is both a cause and consequence of ageing.
Conclusions:
- Transposable elements play a significant role in the ageing process.
- Dysregulation of TEs contributes to age-related diseases.
- Targeting TE activity may offer therapeutic strategies for ageing.
Related Concept Videos
Overview of Transposition and Recombination
15.1K
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...
15.1K
Non-LTR Retrotransposons
11.3K
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...
11.3K
DNA-only Transposons
14.3K
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...
14.3K
LTR Retrotransposons
17.3K
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...
17.3K
piRNA - Piwi-interacting RNAs
6.7K
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...
6.7K
Replication in Eukaryotes
12.8K
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
12.8K


