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Perlin, M. H.

Publications and source records attributed to Perlin, M. H..

3 recordsLinked to original sources

Comparative analysis of lifecycle-dependent A to I RNA editing in three members of the Microbotryum violaceum fungal complex

Microbotryum superbum (MvSup), M. intermedium (MI), and M. lychnidis-dioicae (MVLG) are members of the M. violaceum fungal complex. Each species infects specific host plant species, resulting in what is commonly known as anther smut. The lifecycle of these basidiomycete fungi includes the haploid, mating, and infection stages. RNA editing is a post-transcriptional process where adenosine (A) is converted to inosine (I) by adenosine deaminase enzymes (ADARs); such modifications to RNAs may lead to synonymous and nonsynonymous codon changes, thereby altering protein function. We observed that 57% to 77% of total editing sites created nonsynonymous codon changes in both haploid and mating stages of the three species. Moreover, the a2 haploid strain of MI had fewer editing sites compared to other haploid strains. When we compared amino acid substitutions, we found that in both haploids of MvSup and MVLG, Ala was the preferred codon after nonsynonymous codon changes. Among the edited genes, two were edited only at the mating stage in MvSup, undergoing A to I changes within the regions encoding their functional domains. Differential expression analysis revealed that the gene annotated as Apoptosis-inducing factor-1, was upregulated in MvSup at the mating stage, while another gene, for PHB domain-containing protein responsible for cell proliferation, was downregulated compared to the haploid stage. During all stages of the MvSup lifecycle examined, a specific MAPKKK gene was edited in the portion encoding the PKC-like superfamily domain. Also, that gene was edited at a second site during haploid and mating stages but not during the infection stage. Research on RNA editing in basidiomycetes has been limited and is relatively new. RNA editing mechanisms in fungi have been implicated in fungal pathogenesis, although the exact mechanisms and implications remain unclear. Further research is needed to fully understand functional significance of this apparently ubiquitous process in several members of the Microbotryum fungal complex, with possible ramifications more generally in fungi. Author SummaryEditing of mRNAs after transcription provides another mechanism for selective expression of, especially proteins, under different stages of development or environmental conditions. Here we report on the characterization of A-to-I RNA editing in three species of the Microbotryum violaceum fungal complex, members of the Basidiomycota, where such phenomena have so far been unexplored. We find that such editing is prevalent in different stages throughout the lifecycle of this parasite of plant hosts in the Carnation (Pinks) family. We identified preference for edits that lead to specific amino changes, some of which are limited to one or the other haploid mating-type strains, while others are present preferentially in the mated or plant-infection stages of the lifecycle. Some edits occurred in components of conserved signaling pathways, such as the MAPK pathway, or in genes associated with pathogenicity. Taken together, these results suggest additional hypothesis-driven experiments to further investigate the roles of RNA editing in Microbotryum, providing mechanistic insights into the evolution of species in this fungal complex, as well as for those of other pathogenic fungi.

pathology↗

Repeated loss of function at HD mating-type genes and of recombination suppression without mating-type locus linkage in anther-smut fungi

A wide diversity of mating systems occur in nature, with frequent evolutionary transitions in mating-compatibility mechanisms. Basidiomycete fungi typically have two mating-type loci controlling mating compatibility, HD and PR, usually residing on different chromosomes. In Microbotryum anther-smut fungi, there have been repeated events of linkage between the two mating-type loci through chromosome fusions, leading to large non-recombining regions. By generating high-quality genome assemblies, we found that two sister Microbotryum species parasitizing Dianthus plants, M. superbum and M. shykoffianum, as well as the distantly related M. scorzonarae, have their HD and PR mating-type loci on different chromosomes, but with the PR mating-type chromosome fused with part of the ancestral HD chromosome. Furthermore, progressive extensions of recombination suppression have generated evolutionary strata. In all three species, rearrangements suggest the existence of a transient stage of HD-PR linkage by whole chromosome fusion, and, unexpectedly, the HD genes lost their function. In M. superbum, multiple natural diploid strains were homozygous, and the disrupted HD2 gene was hardly expressed. Mating tests confirmed that a single genetic factor controlled mating compatibility (i.e. PR) and that haploid strains with identical HD alleles could mate and produce infectious hyphae. The HD genes have therefore lost their function in the control of mating compatibility in these Microbotryum species. While the loss of function of PR genes in mating compatibility has been reported in a few basidiomycete fungi, these are the first documented cases for the loss of mating-type determination by HD genes in heterothallic fungi. The control of mating compatibility by a single genetic factor is beneficial under selfing and can thus be achieved repeatedly, through evolutionary convergence in distant lineages, involving different genomic or similar pathways.

evolutionary biology↗

Tempo of degeneration across independently evolved non-recombining regions

Recombination is beneficial over the long term, allowing more effective selection. Despite long-term advantages of recombination, local recombination suppression can evolve and lead to genomic degeneration, in particular on sex chromosomes. Here, we investigated the tempo of degeneration in non-recombining regions, i.e., the function curve for the accumulation of deleterious mutations over time, leveraging on 22 independent events of recombination suppression identified on mating-type chromosomes of anther-smut fungi, including newly identified ones. Using previously available and newly generated high-quality genome assemblies of alternative mating types of 13 Microbotryum species, we estimated degeneration levels in terms of accumulation of non-optimal codons and non-synonymous substitutions in non-recombining regions. We found a reduced frequency of optimal codons in the non-recombining regions compared to autosomes, that was not due to less frequent GC-biased gene conversion or lower ancestral expression levels compared to recombining regions. The frequency of optimal codons rapidly decreased following recombination suppression and reached an asymptote after ca 3 Mya. The strength of purifying selection remained virtually constant at dN/dS = 0.55, i.e. at an intermediate level between purifying selection and neutral evolution. Accordingly, non-synonymous differences between mating-type chromosomes increased linearly with stratum age, at a rate of 0.015 per MY. We thus develop a method for disentangling effects of reduced selection efficacy from GC-biased gene conversion in the evolution of codon usage and we quantify the tempo of degeneration in non-recombining regions, which is important for our knowledge on genomic evolution and on the maintenance of regions without recombination.

evolutionary biology↗