Abstract

Transposable elements (TEs) are constitutive components of both eukaryotic and prokaryotic genomes. The role of TEs in the evolution of genes and genomes has been widely assessed over the past years in a variety of model and non-model organisms. Drosophila is undoubtedly among the most powerful model organisms used for the purpose of studying the role of transposons and their effects on the stability and evolution of genes and genomes. Besides their most intuitive role as insertional mutagens, TEs can modify the transcriptional pattern of host genes by juxtaposing new cis-regulatory sequences. A key element of TE biology is that they carry transcriptional control elements that fine-tune the transcription of their own genes, but that can also perturb the transcriptional activity of neighboring host genes. From this perspective, the transposition-mediated modulation of gene expression is an important issue for the short-term adaptation of physiological functions to the environmental changes, and for long-term evolutionary changes. Here, we review the current literature concerning the regulatory and structural elements operating in cis provided by TEs in Drosophila. Furthermore, we highlight that, besides their influence on both TEs and host genes expression, they can affect the chromatin structure and epigenetic status as well as both the chromosome’s structure and stability. It emerges that Drosophila is a good model organism to study the effect of TE-linked regulatory sequences, and it could help future studies on TE–host interactions in any complex eukaryotic genome.

Highlights

  • Transposable elements (TEs), known as “jumping genes”, are exceptional modifiers of the genome structure and gene expression

  • A key element of TE biology is that they carry transcriptional control elements that fine-tune the transcription of their own genes, but that can perturb the transcriptional activity of neighboring host genes

  • Since their discovery and characterization in eukaryotic genomes in the 1940s [1], TEs have long been regarded as junk DNA, useless and harmful sequences that replicate in the genome with no advantage conferred to the host [2,3]

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Summary

Introduction

Transposable elements (TEs), known as “jumping genes”, are exceptional modifiers of the genome structure and gene expression. Since their discovery and characterization in eukaryotic genomes in the 1940s [1], TEs have long been regarded as junk DNA, useless and harmful sequences that replicate in the genome with no advantage conferred to the host [2,3]. Members of Class I (retrotransposable elements, RTE) transpose via reverse transcription of an RNA intermediate that is afterward integrated into a new genomic locus. TEs belonging to Class II are called DNA transposons They contain terminal inverted repeats (TIRs), flanking the transposase gene that encodes an integrase essential to perform the transposition step, known as the cut-and-paste mechanism. D. melanogaster is currently widely used as an animal model to study the most diverse aspects of genetics, from basic inheritance to cancer [9], but additional genomic resources are continuously developed for other species of the Drosophila genus that will soon become model species in specific fields of investigation [13,14,15,16,17]

Drosophila TEs: A Brief Overview
TEs as Promoter Suppliers
Additional Cis-Regulatory Transcriptional Signals within TE
Structural Role of Cis-Operating Sequences within TEs
Findings
Conclusions and Future Directions
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