Evolved and Plastic Gene Expression in Adaptation of a Specialist Fly to a Novel Niche

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rachel A. Steward, Jesús Ortega Giménez, Shruti Choudhary, Oliver Moss, Yi Su, Olivier Van Aken, Anna Runemark
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Abstract

How gene expression evolves to enable divergent ecological adaptation and how changes in gene expression relate to genomic architecture are pressing questions for understanding the mechanisms enabling adaptation and ecological speciation. Furthermore, how plasticity in gene expression can both contribute to and be affected by the process of ecological adaptation is crucial to understanding gene expression evolution, colonisation of novel niches and response to rapid environmental change. Here, we investigate the role of constitutive and plastic gene expression differences between host races, or host-specific ecotypes, of the peacock fly Tephritis conura, a thistle bud specialist. By cross-fostering larvae to new buds of their natal host plant or the alternative, novel host plant, we uncover extensive constitutive differences in gene expression between the host races, especially genes associated with processing of host plant chemicals. However, evidence for expression plasticity was minimal and limited to the ancestral host race. Genes with host race-specific expression are found more often than expected within a large inversion in the T. conura genome, adding to evidence that inversions are important for enabling diversification in the face of gene flow and underscores that altered gene expression may be key to understanding the evolutionary consequences of inversions.

Abstract Image

果蝇适应新生态位的进化和可塑性基因表达。
基因表达如何进化以实现不同的生态适应,以及基因表达的变化如何与基因组结构相关,是理解适应和生态物种形成机制的紧迫问题。此外,基因表达的可塑性如何促进和受生态适应过程的影响,对于理解基因表达进化、新生态位的定植和对快速环境变化的反应至关重要。在这里,我们研究了组成性和可塑性基因表达差异在宿主种族或宿主特定生态型之间的作用,孔雀飞Tephritis conura,一个蓟花蕾专家。通过将幼虫培育到其原生寄主植物或替代的新寄主植物的新芽中,我们发现了寄主种族之间基因表达的广泛构成差异,特别是与寄主植物化学物质处理相关的基因。然而,表达可塑性的证据很少,而且仅限于祖先宿主种族。具有宿主种族特异性表达的基因在conura基因组的一个大反转中被发现的频率比预期的要高,这进一步证明了在面对基因流时,反转对于实现多样化很重要,并强调了基因表达的改变可能是理解反转的进化后果的关键。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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