Genome organization and gene expression shape the transposable element distribution in the Drosophila melanogaster euchromatin

Autor: Pierre Fontanillas, Max Reuter, Daniel L. Hartl
Jazyk: angličtina
Rok vydání: 2007
Předmět:
Transposable element
Cancer Research
Genome evolution
Transcription
Genetic

Euchromatin
lcsh:QH426-470
Eukaryotes
Pseudogene
Genome
Insect

Biology
Genome
03 medical and health sciences
0302 clinical medicine
Genes
X-Linked

Untranslated Regions
Gene density
Genetics
Animals
Arthropods
Molecular Biology
Gene
Conserved Sequence
Genetics (clinical)
Ecology
Evolution
Behavior and Systematics

030304 developmental biology
Genomic organization
Evolutionary Biology
0303 health sciences
Base Sequence
food and beverages
Genetics and Genomics
Introns
Insects
lcsh:Genetics
Drosophila melanogaster
Germ Cells
Gene Expression Regulation
Multigene Family
DNA Transposable Elements
Drosophila
DNA
Intergenic

030217 neurology & neurosurgery
Research Article
DNA Transposable Elements/genetics
DNA
Intergenic/genetics

Drosophila melanogaster/genetics
Euchromatin/genetics
Gene Expression Regulation/genetics
Genome
Insect/genetics

Germ Cells/metabolism
Introns/genetics
Untranslated Regions/genetics
Zdroj: PLoS Genetics, Vol 3, Iss 11, p e210 (2007)
PLoS Genetics, vol. 3, no. 11, pp. e210
PLoS Genetics
ISSN: 1553-7404
1553-7390
Popis: The distribution of transposable elements (TEs) in a genome reflects a balance between insertion rate and selection against new insertions. Understanding the distribution of TEs therefore provides insights into the forces shaping the organization of genomes. Past research has shown that TEs tend to accumulate in genomic regions with low gene density and low recombination rate. However, little is known about the factors modulating insertion rates across the genome and their evolutionary significance. One candidate factor is gene expression, which has been suggested to increase local insertion rate by rendering DNA more accessible. We test this hypothesis by comparing the TE density around germline- and soma-expressed genes in the euchromatin of Drosophila melanogaster. Because only insertions that occur in the germline are transmitted to the next generation, we predicted a higher density of TEs around germline-expressed genes than soma-expressed genes. We show that the rate of TE insertions is greater near germline- than soma-expressed genes. However, this effect is partly offset by stronger selection for genome compactness (against excess noncoding DNA) on germline-expressed genes. We also demonstrate that the local genome organization in clusters of coexpressed genes plays a fundamental role in the genomic distribution of TEs. Our analysis shows that—in addition to recombination rate—the distribution of TEs is shaped by the interaction of gene expression and genome organization. The important role of selection for compactness sheds a new light on the role of TEs in genome evolution. Instead of making genomes grow passively, TEs are controlled by the forces shaping genome compactness, most likely linked to the efficiency of gene expression or its complexity and possibly their interaction with mechanisms of TE silencing.
Author Summary Transposable elements (TEs) are parasitic DNA segments that can move within a host genome. These selfish mobile elements are present in virtually all eukaryote species and can contribute significantly to their DNA. TEs multiply by copying themselves within the genome. Depending on where they land, new copies can alter the organism's phenotype, often negatively but sometimes positively. Although TEs have some preferences, they have few opportunities to choose their landing places. It has been proposed that new copies arise in places that are easily accessible to their insertion. Increased accessibility can occur close to genes that are actively transcribed, because the DNA is uncoiled and laid bare. We have tested whether this effect has a detectable influence on the distribution of TEs in the genome of the fruitfly, D. melanogaster. Our analysis shows that this is indeed the case. Thus, TE insertions are denser around genes expressed in the cells that give rise to sperm and eggs (the germline). This is expected because only those new copies arising in these cells are transmitted to future generations. In addition, we found that genomic regions vary in their tolerance to insertions. Thus, TEs are rare wherever a considerable increase in noncoding DNA is deleterious.
Databáze: OpenAIRE