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Meiotic effects ofMSH4copy number variation support an adaptive role for post-polyploidy gene loss

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ABSTRACTMany eukaryotes descend from polyploid ancestors that experienced massive duplicate gene loss. This genomic erosion is particularly strong for duplicated (meiotic) recombination genes that return to a single copy more rapidly than genome average following polyploidy. To better understand the evolutionary forces underlying duplicate loss, we analysed how varying copy numbers ofMSH4, an essential meiotic recombination gene, influences crossover formation in allotetraploidBrassica napus. We show that faithful chromosome segregation and crossover frequencies between homologous chromosomes are unchanged withMSH4duplicate loss; by contrast, crossovers between homoeologous chromosomes (which result in genomic rearrangements) decrease with reductions inMSH4copy number. We also found that inter-homoeologue crossovers originate almost exclusively from the MSH4-dependent crossover pathway. Limiting the efficiency of this pathway by decreasing the copy number of key meiotic recombination genes could therefore contribute to adaptation to polyploidy, by promoting regular chromosome segregation and genomic stability.
Title: Meiotic effects ofMSH4copy number variation support an adaptive role for post-polyploidy gene loss
Description:
ABSTRACTMany eukaryotes descend from polyploid ancestors that experienced massive duplicate gene loss.
This genomic erosion is particularly strong for duplicated (meiotic) recombination genes that return to a single copy more rapidly than genome average following polyploidy.
To better understand the evolutionary forces underlying duplicate loss, we analysed how varying copy numbers ofMSH4, an essential meiotic recombination gene, influences crossover formation in allotetraploidBrassica napus.
We show that faithful chromosome segregation and crossover frequencies between homologous chromosomes are unchanged withMSH4duplicate loss; by contrast, crossovers between homoeologous chromosomes (which result in genomic rearrangements) decrease with reductions inMSH4copy number.
We also found that inter-homoeologue crossovers originate almost exclusively from the MSH4-dependent crossover pathway.
Limiting the efficiency of this pathway by decreasing the copy number of key meiotic recombination genes could therefore contribute to adaptation to polyploidy, by promoting regular chromosome segregation and genomic stability.

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