grant

The Genomic Basis and Molecular Mechanisms of Speciation

Organization SYRACUSE UNIVERSITYLocation SYRACUSE, UNITED STATESPosted 19 Sept 2022Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY2025AffectBacterial Fertility FactorBacterial Sex FactorBiologic ModelsBiological ModelsBiologyCell FunctionCell PhysiologyCell ProcessCellular FunctionCellular PhysiologyCellular ProcessComplexCoupledCreativenessDNA mutationDataDrosophilaDrosophila genusDysfunctionF FactorF PlasmidsFunctional disorderGenesGeneticGenetic ChangeGenetic DifferentiationGenetic DivergenceGenetic DiversityGenetic DriftGenetic TechnicsGenetic TechniquesGenetic VariationGenetic defectGenetic mutationGenomeGenomicsGoalsHybridsMale SterilityModel SystemMolecularMolecular GeneticsMutationPartner in relationshipPathway interactionsPhysiopathologyPopulationProcessProteomicsResearchResistance Transfer FactorSex Factor FSterilitySubcellular ProcessSubgroupX ChromosomeY Chromosomecreativityfertility factorfruit flygenome mutationhuman diseaseimprovedinnovateinnovationinnovativemale fertilitymatememberpathophysiologypathwayreproductivesex factorsteriletooltraittranscriptomics
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

PROJECT SUMMARY
One of the fundamental problems in evolutionary biology is to understand the molecular genetic basis of

speciation. Recent advances in speciation research have improved our understanding of interspecific divergence,

but we still lack a comprehensive understanding of the molecular processes that diverge among incipient species.

In the handful of cases where the genetic mechanisms of reproductive isolation have been elucidated, these

invariably tackle late-evolving and/or hybrid dysfunction. This means that we still lack a general understanding

of the molecular processes that govern pre-zygotic reproductive barriers, even though these are often important

early in the speciation process.

My lab will tackle this problem by identifying the molecular genetic basis of pre-zygotic and post-zygotic re-

productive isolation between members of the Drosophila virilis species sub-group. This species group provides

an especially unique opportunity to dissect the genetic and molecular mechanisms of pre-zygotic barriers, as

members of this group are prone to evolve these types of barriers quickly between species and even among

populations of the same species. Our overall approach integrates several strategies to answer the following

questions: What are the genetic mechanisms that cause reproductive isolation between species? Which molec-

ular and cellular processes are affected by divergence of these genetic mechanisms? What are the evolutionary

forces that drive divergence of the relevant genes between species? What is the landscape of natural genetic

variation within and between species that facilitates evolutionary divergence of these genes?

The first project within this proposal will focus on post-mating pre-zygotic barriers (i.e., gametic incompatibil-

ities). I have previously shown that gametic incompatibilities are rampant in the D. virilis sub-group, and that the

genetic basis is moderately complex but highly tractable using a combination of molecular genetics techniques

coupled with transcriptomic and proteomic analyses of reproductive traits. The second project will tackle the

mechanisms of hybrid male sterility that are caused by incompatibilities between the Y and X chromosomes.

The Drosophila Y chromosome carries several male fertility factors, but it has seldom been directly implicated in

interspecific hybrid sterility between closely related species. Our preliminary data show that the Y chromosome

is necessary and sufficient to cause sterility in hybrids.

The research in this proposal will be innovative because we will deploy cutting edge tools in creative ways that

will allow us to dissect complex genetic mechanisms in a newly established model system.

Grant Number: 5R35GM147454-04
NIH Institute/Center: NIH

Principal Investigator: Yasir Ahmed-Braimah

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →