bioRxiv Science⌕ Search

bioRxiv · 10.1101/2023.03.02.530769

Genome biology and evolution of mating type loci in four cereal rust fungi

Abstract

Obligate heterozygous loci such as sex- or mating-compatibility regions often display suppression of recombination and signals of genomic degeneration. In Basidiomycota, two distinct gene loci confer mating compatibility. These encode for homeodomain (HD) transcription factors and pheromone receptor (Pra)-ligand pairs. To date genome level mating type (MAT) loci analysis is lacking for obligate biotrophic basidiomycetes in the order Pucciniales, which contains many economically important plant pathogens. Here, we focus on four Puccinia cereal rust species, including P. coronata f. sp. avenae, Puccinia graminis f. sp. tritici, P. triticina and P. striiformis f. sp. tritici, which infect oat and wheat. MAT loci are located on two separate chromosomes supporting previous hypotheses of tetrapolar mating types in the Pucciniales. The HD locus is multiallelic in all four species while the PR locus appears to be biallelic except for P. graminis f. sp. tritici which displays genetic features of more than two alleles. HD loci were largely conserved in their macrosynteny within and between species without strong signals of recombination suppression. PR loci proximate regions, however, displayed extensive signs of recombination suppression and genomic degeneration in the three species with a clear biallelic PR locus. These observations suggest a correlation between recombination suppression, genomic degeneration and allele status of MAT loci which is consistent with recent mathematical modelling and simulations. Finally, we confirm the evolutionary conservation of MAT gene expression during the asexual infection cycle of the cereal host which we propose is related to correct nuclear pairing during spore formation. Together, our study provides insights into the evolution of MAT loci of key pathogenic Puccinia species. This detailed understanding is important to predict possible combinations of nuclear pairs that can arise via sexual reproduction or somatic recombination to enable the evolution of newly virulent isolates of these important plant pathogens. Author summarySex of animals and some plants is determined by sex chromosomes. In fungi, mate compatibility is determined by mating type (MAT) loci, which share some features with sex chromosomes including recombination suppression around heterozygous loci. Here, we study the MAT loci in fungal pathogens from the order Pucciniales that can cause rust diseases on many economically important plants including wheat and oat. We show that one of the MAT loci is multiallelic, while the other is biallelic. The biallelic locus shows strong signs of recombination suppression and genetic deterioration with an increase in transposable elements and gene deserts surrounding the locus. Our findings on the genome biology of MAT loci in four economically important pathogens will lead to a better understanding and prediction of evolution of novel virulent isolates that can lead to large scale pandemics in agriculture.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Luo, Z., McTaggart, A. R., Schwessinger, B.. 2023-03-02. Genome biology and evolution of mating type loci in four cereal rust fungi. https://doi.org/10.1101/2023.03.02.530769

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Denisovan introgression left differential selection regimes in Humans and Neanderthals on the SLC30A9 gene

Signals of positive selection around the SLC30A9 gene have been reported in human populations outside Africa. Selection likely acted on a highly differentiated single-nucleotide polymorphism, rs1047626, leading to a non-synonymous substitution in the encoded zinc transporter. Because of the striking similarity between the putatively selected SLC30A9 haplotype observed in several current human populations and the Denisovan individual, previous work has proposed adaptive introgression. Yet alternative explanations, including ancient human variation, and the precise archaic source -Neanderthal or Denisovan- remained unresolved. Considering the potentially complex evolution of SLC30A9, we applied Approximate Bayesian Computation (ABC) algorithms coupled to machine learning to investigate the most plausible evolutionary origin of this substitution. After modelling different evolutionary scenarios with forward-in-time simulations, our results highlight that the most probable scenario is a Denisovan origin of the rs1047626 polymorphism. However, the allele likely introgressed into Neanderthals first and was then passed into non-African modern humans. Moreover, the derived allele frequency for rs1047626 across several African populations is consistent with back-to-Africa migrations. Finally, our ABC analyses indicate strong positive selection in East Asian populations and other out-of-Africa populations, whereas in Neanderthal populations, the selection coefficient was probably neutral or slightly deleterious.

evolutionary biology↗

RELAX does not reproduce its own estimates at default settings, and its output does not show it

Selection-intensity estimates from RELAX are reported as a point value of K with a likelihood-ratio P. We report that, at default settings and on data of ordinary size, the program does not reproduce its own fits. Of 27 enzyme entries refitted under two optimiser configurations, none reproduced its log-likelihood to within 0.01 units; the median change was 103 units, the largest over 3,400, and four verdicts reversed. Eighty null orthologues reproduced none. A byte-identical command returned a distinct likelihood on every repetition, single-threaded, across three releases, and on alignments simulated under the fitted model, where 3.3 per cent of replicates reproduced. The documented random-number seed never reaches the generator when assigned on the command line, yet reads back as the value supplied. PAML localises the cause: its two-ratio model, without site classes, reproduced its log-likelihood for all 288 genes; its site-class models agreed for 27 to 67 per cent. The instability follows the mixture over sites, not the program. The output does not show it: 46 of 410 fits ended with a negative likelihood-ratio statistic, impossible under convergence, and 123 of 410 report a K re-estimated under a domain restriction rather than the unconstrained maximum. Of 234 published studies using RELAX, none reported a seed. Seeding while holding the thread count at one reproduced sixty of sixty runs on twenty genes under two releases; the seed alone reproduced none of five, and no documentation states the second condition. We recommend that fits be repeated and their dispersion published.

evolutionary biology↗

Sequential accumulation of adaptive alleles forms an inversion supergene in deer mice

Supergenes are clusters of co-inherited loci that affect multiple or complex phenotypes. Despite the growing number of chromosomal inversions identified as supergenes in natural populations, their molecular basis and evolutionary history often remain obscure. Here, we identified two candidate genes, Slc45a2 and Npr3, within a 41-Mb inversion supergene in the deer mouse (Peromyscus maniculatus) that respectively drive darker coats and longer tails - two traits associated with forest adaptation. Mice homozygous for the inversion (inv/inv) exhibit elevated Slc45a2 expression in melanocytes relative to the congenic standard genotype (std/std), disrupting pheomelanin production. In parallel, downregulation of Npr3 in inv/inv mouse growth plates prolongs postnatal growth of caudal vertebrae, resulting in tail elongation. Population-level analyses further implicate that this supergene arose through the subsequent accumulation of the Npr3 allele within the inversion, rather than by capturing all beneficial mutations at its origin.

evolutionary biology↗