Abstract:Interspecific hybridization is often seen as a genomic stress that may lead to new gene expression patterns and deregulation of transposable elements (TEs). The understanding of expression changes in hybrids compared to parental species is essential to disentangle their putative role in speciation processes. However, to date we ignore the detailed mechanisms involved in genomic deregulation in hybrids. We studied the ovarian transcriptome and epigenome of the Drosophila buzzatii and Drosophila koepferae specie… Show more
“…In our study, we performed Nanopore sequencing for seven cactophilic Drosophila species/subspecies. Both genomes of D. buzzatii and D. koepferae had 175 Mb of estimated genome sizes, which is similar with 160 Mb and 169 Mb obtained on previously assemblies (46,61), performed through the combination of short and long reads technologies. Furthermore, we obtained 11,347 and 11,440 fully annotated genes in D. buzzatii and D. koepferae , which is very similar with the previous 10,983 and 11,804 obtained for the same species.…”
Section: Discussionsupporting
confidence: 84%
“…The resolution of gene annotation for D. arizonae was similar to D. mojavensis subspecies due to the recent (1.5 Mya) divergence between them (43), whereas for D. buzzatii and D. koepferae it was ~23% smaller compared to D. mojavensis, as expected since they are more distant related species (44). Similar amount of genes had been annotated previously in the D. buzzatii (45,46) and D. koepferae (46,40) genomes. Since analysis on HLAU genes is the focus of this study, their efficient annotation is relevant.…”
Section: Genome Assemblies and Gene Annotationsupporting
confidence: 74%
“…obtained on previously assemblies(46,61), performed through the combination of short and long reads technologies. Furthermore, we obtained 11,347 and 11,440 fully annotated genes in D. buzzatii and D. koepferae, which is very similar with the previous 10,983and 11,804 obtained for the same species.…”
BackgroundThe host shift in insects has been considered a key process with potential to collaborate with ecological speciation. Both genomics and transcriptomics variation has been attributed to such process, in which gene families with functions for host location, acceptance and usage have been proposed to evolve. In this context, cactophilicDrosophilaspecies are an excellent model to study host shift effects, since they use a wide-range of cacti as hosts, and many species have cacti-hosts preference. Despite the potential adaptive role of TEs by generating genetic variability between species and populations, the extent of TEs′ contribution to host shift remains unexplored.ResultsHere, we performed genomics and transcriptomics analyses in seven genomes of cactophilic species/subspecies to investigate how TEs interact with genes likely to be associated with host shift. Our results revealed transposition bursts between species, and an enrichment of TEs at promoter regions of host shift-related genes. Pairwise differential expression analysis between species with different preferential hosts in larvae and head tissues demonstrated divergence on gene expression associated with host location in head, whereas for the larvae we found higher differential expression of genes related to usage/detoxification. Although TEs′ presence does not affect overall gene expression, we observed 2.1% of genes generating gene-TE chimeric transcripts, including those with function affecting host preference. In addition, Helitrons were often observed interacting with genes as a cis-regulatory element.ConclusionsOur combined genomics and transcriptomics approaches provide new insights regarding the evolutionary role of TEs on the context of ecological speciation.
“…In our study, we performed Nanopore sequencing for seven cactophilic Drosophila species/subspecies. Both genomes of D. buzzatii and D. koepferae had 175 Mb of estimated genome sizes, which is similar with 160 Mb and 169 Mb obtained on previously assemblies (46,61), performed through the combination of short and long reads technologies. Furthermore, we obtained 11,347 and 11,440 fully annotated genes in D. buzzatii and D. koepferae , which is very similar with the previous 10,983 and 11,804 obtained for the same species.…”
Section: Discussionsupporting
confidence: 84%
“…The resolution of gene annotation for D. arizonae was similar to D. mojavensis subspecies due to the recent (1.5 Mya) divergence between them (43), whereas for D. buzzatii and D. koepferae it was ~23% smaller compared to D. mojavensis, as expected since they are more distant related species (44). Similar amount of genes had been annotated previously in the D. buzzatii (45,46) and D. koepferae (46,40) genomes. Since analysis on HLAU genes is the focus of this study, their efficient annotation is relevant.…”
Section: Genome Assemblies and Gene Annotationsupporting
confidence: 74%
“…obtained on previously assemblies(46,61), performed through the combination of short and long reads technologies. Furthermore, we obtained 11,347 and 11,440 fully annotated genes in D. buzzatii and D. koepferae, which is very similar with the previous 10,983and 11,804 obtained for the same species.…”
BackgroundThe host shift in insects has been considered a key process with potential to collaborate with ecological speciation. Both genomics and transcriptomics variation has been attributed to such process, in which gene families with functions for host location, acceptance and usage have been proposed to evolve. In this context, cactophilicDrosophilaspecies are an excellent model to study host shift effects, since they use a wide-range of cacti as hosts, and many species have cacti-hosts preference. Despite the potential adaptive role of TEs by generating genetic variability between species and populations, the extent of TEs′ contribution to host shift remains unexplored.ResultsHere, we performed genomics and transcriptomics analyses in seven genomes of cactophilic species/subspecies to investigate how TEs interact with genes likely to be associated with host shift. Our results revealed transposition bursts between species, and an enrichment of TEs at promoter regions of host shift-related genes. Pairwise differential expression analysis between species with different preferential hosts in larvae and head tissues demonstrated divergence on gene expression associated with host location in head, whereas for the larvae we found higher differential expression of genes related to usage/detoxification. Although TEs′ presence does not affect overall gene expression, we observed 2.1% of genes generating gene-TE chimeric transcripts, including those with function affecting host preference. In addition, Helitrons were often observed interacting with genes as a cis-regulatory element.ConclusionsOur combined genomics and transcriptomics approaches provide new insights regarding the evolutionary role of TEs on the context of ecological speciation.
“…Even though we noticed that changes in expression of few specific TE families could be explained by their small RNA amount changes after heat stress, we did not detect this clear association globally, which was in concordance with other studies ( Funikov et al 2015 ; Fast et al 2017 ) and highlighted that other mechanisms could also be involved in this activation. For example, changes in the epigenome affecting TE expression under the genomic stress have been observed previously ( Bodelón et al 2022 ). Specifically, Hsp83 was described to be involved in epigenetic modification ( Tariq et al 2009 ), as well as other changes in the epigenome have been observed after a heat stress ( Arrigo 1983 ; Pauli et al 1992 ).…”
Global warming is forcing insect populations to move and adapt, triggering adaptive genetic responses. Thermal stress is known to alter gene expression, repressing the transcription of active genes, and inducing others, such as those encoding heat shock proteins. It has also been related to the activation of some specific Transposable Element (TE) families. However, the actual magnitude of this stress on the whole genome and the factors involved in these genomic changes are still unclear. We studied mRNAs and small RNAs in gonads of two Drosophila subobscura populations, considered a good model to study adaptation to temperature changes. In control conditions, we found that a few genes and TE families were differentially expressed between populations, pointing out their putative involvement in the adaptation of populations to their different environments. Under heat stress, sex specific changes in gene expression together with a trend towards overexpression, mainly of heat shock response-related genes were observed. We did not observe large changes of TE expression nor small RNA production due to stress. Only population and sex-specific expression changes of some TE families (mainly retrotransposons), or the amounts of siRNAs and piRNAs, derived from specific TE families were observed, as well as the piRNA production from some piRNA clusters. Changes in small RNA amounts and TE expression could not be clearly correlated, indicating that other factors as chromatin modulation, could also be involved. This work provides the first whole transcriptomic study including genes, TEs and small RNAs after a heat stress in D. subobscura.
Gene expression has a key role in reproductive isolation, and studies of hybrid gene expression have identified mechanisms causing hybrid sterility. Here, we review the evidence for altered gene expression following hybridization and outline the mechanisms shown to contribute to altered gene expression in hybrids. Transgressive gene expression, transcending that of both parental species, is pervasive in early generation sterile hybrids, but also frequently observed in viable, fertile hybrids. We highlight studies showing that hybridization can result in transgressive gene expression, also in established hybrid lineages or species. Such extreme patterns of gene expression in stabilized hybrid taxa suggest that altered hybrid gene expression may result in hybridization‐derived evolutionary novelty. We also conclude that while patterns of misexpression in hybrids are well documented, the understanding of the mechanisms causing misexpression is lagging. We argue that jointly assessing differences in cell composition and cell‐specific changes in gene expression in hybrids, in addition to assessing changes in chromatin and methylation, will significantly advance our understanding of the basis of altered gene expression. Moreover, uncovering to what extent evolution of gene expression results in altered expression for individual genes, or entire networks of genes, will advance our understanding of how selection moulds gene expression. Finally, we argue that jointly studying the dual roles of altered hybrid gene expression, serving both as a mechanism for reproductive isolation and as a substrate for hybrid ecological adaptation, will lead to significant advances in our understanding of the evolution of gene expression.
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