X-chromosome driven speciation through testes-expressed genes: comparative population genomics meets scRNA analysis in primates
This project aims to identify genes driving rapid X chromosome evolution and reproductive barriers in primates through population genomics and single-cell RNA sequencing during spermatogenesis.
Projectdetails
Introduction
Primate X chromosomes evolve extraordinarily fast and are also tightly associated with the establishment of reproductive barriers between emerging species.
Hypothesis
The hypothesis of this proposal is that genetic conflicts between the X chromosome and the rest of the genome during spermatogenesis cause rapid X chromosome evolution and build reproductive barriers. Genetic conflicts for transmission to haploid gametes, called meiotic drive, will cause non-adaptive evolution, which is expected to be countered by other genomic elements that will then be under selection. Such an arms race is expected to lead to a very rapid evolution of the X chromosome and a fast accumulation of incompatibilities between isolated populations, leading to speciation.
Project Goal
The goal of the project is to identify the underlying mechanisms and the genes responsible for meiotic drive using primates as the study system. A priori candidate processes include:
- X-linked genes under repeated fast evolution
- Focus on genes targeted by pachytene piRNAs
- Investigation of ampliconic genes
Population genomics analysis will generate specific hypotheses that will then be tested by following the expression of candidate genes during spermatogenesis through scRNAseq. Findings will be validated by ultrasensitive, in situ staining of single transcripts and immunohistochemistry. Finally, the behavior of key genes and processes will then be investigated in incipient speciation events.
Methodology
Specifically, 850 individuals of 250 species of primates with full genome data will be analyzed for candidate genes on the X chromosome. These genes will be investigated in large-scale comparative scRNA sequencing analyses of over 10,000 individual testicular cells from 14 primate species, including all great ape species. This approach allows expression trajectories through spermatogenesis to be inferred and followed up in functional experiments.
Success Criterion
The success criterion is to report on primate speciation genes together with their biological mode of action.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.499.369 |
Totale projectbegroting | € 2.499.369 |
Tijdlijn
Startdatum | 1-10-2022 |
Einddatum | 30-9-2027 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- AARHUS UNIVERSITETpenvoerder
Land(en)
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This project aims to uncover the genetic basis of human adaptation by using hybrid cells and MPRAs to map cis-regulatory changes and their impact on gene expression and phenotypes.
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