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Gene expression and alternative splicing contribute to adaptive divergence of ecotypes

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DOI: 10.1038/s41437-023-00665-y

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Regulation of gene expression is a critical link between genotype and phenotype, and alternative splicing plays an essential role in plants, potentially providing a source of evolutionary novelty. This study examines the relationship between alternative splicing, gene expression levels, and adaptation in dune-adapted prairie sunflowers. The results show that alternative splicing and gene expression levels are differentiated among ecotypes, even in a common environment, indicating the importance of alternative splicing in natural selection.
Regulation of gene expression is a critical link between genotype and phenotype explaining substantial heritable variation within species. However, we are only beginning to understand the ways that specific gene regulatory mechanisms contribute to adaptive divergence of populations. In plants, the post-transcriptional regulatory mechanism of alternative splicing (AS) plays an important role in both development and abiotic stress response, making it a compelling potential target of natural selection. AS allows organisms to generate multiple different transcripts/proteins from a single gene and thus may provide a source of evolutionary novelty. Here, we examine whether variation in alternative splicing and gene expression levels might contribute to adaptation and incipient speciation of dune-adapted prairie sunflowers in Great Sand Dunes National Park, Colorado, USA. We conducted a common garden experiment to assess transcriptomic variation among ecotypes and analyzed differential expression, differential splicing, and gene coexpression. We show that individual genes are strongly differentiated for both transcript level and alternative isoform proportions, even when grown in a common environment, and that gene coexpression networks are disrupted between ecotypes. Furthermore, we examined how genome-wide patterns of sequence divergence correspond to divergence in transcript levels and isoform proportions and find evidence for both cis and trans-regulation. Together, our results emphasize that alternative splicing has been an underappreciated mechanism providing source material for natural selection at short evolutionary time scales.

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