Abstract

BackgroundHybridization among Louisiana Irises has been well established and the genetic architecture of reproductive isolation is known to affect the potential for and the directionality of introgression between taxa. Here we use co-dominant markers to identify regions where QTL are located both within and between backcross maps to compare the genetic architecture of reproductive isolation and fitness traits across treatments and years.ResultsQTL mapping was used to elucidate the genetic architecture of reproductive isolation between Iris fulva and Iris brevicaulis. Homologous co-dominant EST-SSR markers scored in two backcross populations between I. fulva and I. brevicaulis were used to generate genetic linkage maps. These were used as the framework for mapping QTL associated with variation in 11 phenotypic traits likely responsible for reproductive isolation and fitness. QTL were dispersed throughout the genome, with the exception of one region of a single linkage group (LG) where QTL for flowering time, sterility, and fruit production clustered. In most cases, homologous QTL were not identified in both backcross populations, however, homologous QTL for flowering time, number of growth points per rhizome, number of nodes per inflorescence, and number of flowers per node were identified on several linkage groups.ConclusionsTwo different traits affecting reproductive isolation, flowering time and sterility, exhibit different genetic architectures, with numerous QTL across the Iris genome controlling flowering time and fewer, less distributed QTL affecting sterility. QTL for traits affecting fitness are largely distributed across the genome with occasional overlap, especially on LG 4, where several QTL increasing fitness and decreasing sterility cluster. Given the distribution and effect direction of QTL affecting reproductive isolation and fitness, we have predicted genomic regions where introgression may be more likely to occur (those regions associated with an increase in fitness and unlinked to loci controlling reproductive isolation) and those that are less likely to exhibit introgression (those regions linked to traits decreasing fitness and reproductive isolation).

Highlights

  • Hybridization among Louisiana Irises has been well established and the genetic architecture of reproductive isolation is known to affect the potential for and the directionality of introgression between taxa

  • By examining the direction of QTL effects for traits influencing reproductive isolation and fitness, QTL mapping studies can be used to predict both regions of the genome that are resistant to introgression, as well as genomic regions that are more likely to introgress

  • Several different traits revealed QTL that colocalized in the same locations, most notably in the BCIB map where QTL for five traits can be found to colocalize on linkage group (LG) 4

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Summary

Introduction

Hybridization among Louisiana Irises has been well established and the genetic architecture of reproductive isolation is known to affect the potential for and the directionality of introgression between taxa. The potential for introgression of genomic regions influencing quantitative variation between species is dependent on the underlying genetic architecture (such as the number of loci, the magnitude and effect of each locus, and interactions between loci) of the diverse isolating barriers preventing gene flow between the hybridizing (even rarely hybridizing) species [11]. Following the genic view of speciation, differences in a relatively small number of loci are sufficient to establish isolation between species [17]) While these loci (‘speciation genes’) are not free to move across species boundaries due to negative fitness effects when placed in a heterologous genetic background, the portions of the genome that are not linked to these loci could potentially be tolerant to introgression [17,18]. By examining the direction of QTL effects for traits influencing reproductive isolation and fitness, QTL mapping studies can be used to predict both regions of the genome that are resistant to introgression (potentially identifying regions tightly linked to ‘speciation genes’), as well as genomic regions that are more likely to introgress (regions of the genome that introgress with neutral or positive effects on fitness)

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