Functional dissection and assembly of a small, newly evolved, W chromosome-specific genomic region of the African clawed frog Xenopus laevis.
Caroline M S CauretDanielle C JordanLindsey M KukolySarah R BurtonEmmanuela U AneleJacek M KwiecienMarie-Theres GansaugeSinthu SenthillmohanEli GreenbaumMatthias MeyerMarko E HorbBen J EvansPublished in: PLoS genetics (2023)
Genetic triggers for sex determination are frequently co-inherited with other linked genes that may also influence one or more sex-specific phenotypes. To better understand how sex-limited regions evolve and function, we studied a small W chromosome-specific region of the frog Xenopus laevis that contains only three genes (dm-w, scan-w, ccdc69-w) and that drives female differentiation. Using gene editing, we found that the sex-determining function of this region requires dm-w but that scan-w and ccdc69-w are not essential for viability, female development, or fertility. Analysis of mesonephros+gonad transcriptomes during sexual differentiation illustrates masculinization of the dm-w knockout transcriptome, and identifies mostly non-overlapping sets of differentially expressed genes in separate knockout lines for each of these three W-specific gene compared to wildtype sisters. Capture sequencing of almost all Xenopus species and PCR surveys indicate that the female-determining function of dm-w is present in only a subset of species that carry this gene. These findings map out a dynamic evolutionary history of a newly evolved W chromosome-specific genomic region, whose components have distinctive functions that frequently degraded during Xenopus diversification, and evidence the evolutionary consequences of recombination suppression.
Keyphrases
- genome wide
- copy number
- dna methylation
- genome wide identification
- cell free
- single cell
- computed tomography
- gene expression
- glycemic control
- type diabetes
- mental health
- skeletal muscle
- mass spectrometry
- cross sectional
- metabolic syndrome
- rna seq
- genome wide analysis
- dna damage
- high resolution
- transcription factor
- molecularly imprinted
- tandem mass spectrometry
- high density
- insulin resistance
- oxidative stress
- simultaneous determination
- wild type