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Hybridization in bryophytes involves a fusion of gametes produced by haploid parental gametophytes of different species. The primary hybrid is thus the short-lived diploid sporophyte, which soon undergoes meiosis prior to the formation of large amounts of haploid spores. We compared morphology of gametophytes (branch leaves) and sporophytes (capsule inclination) from sympatric populations and allopatric populations of H. lutescens and H. sericeum. In addition, we used transcriptome data to select 85 nuclear SNP markers that were fixed for alternative alleles in the two species. The SNPs were used to estimate the degree of hybridization in diploid sporophytes. Our study shows that gametophytes from sympatric populations display intermediate morphology in a number of leaf characters, with exception for leaf sizes, which are markedly smaller than those in allopatric populations. None of the 100 sporophytes appeared to be primary hybrids, but 33 displayed admixing—heterozygotic expression of SNP markers or mismatch of occasional markers in homozygous condition—suggesting that extensive introgression takes place in the sympatric populations. Most sporophytes with intermediate capsule inclination, initially classed as putative hybrids, did not display admixture of nuclear SNP markers. Sixty-seven percent of admixed sporophytes have predominantly nuclear SNPs typical for H. lutescens. Our results suggest that interspecific hybridization and bidirectional introgression are relatively common in the studied sympatric populations, giving rise to viable recombinants, but not complete mixing of the parental genomes. Our study is one of the first detailed accounts of hybridization among pleurocarpous mosses, opening for future studies of gene transfer and introgression between bryophyte lineages and its role in local adaptation and long-term evolutionary diversification. [ABSTRACT FROM AUTHOR]

This work presents a detailed investigation of the genomic region surrounding the PRNP gene in a sample of patients diagnosed with fatal familial insomnia (FFI) from several European countries, notably Spain. The main focus of the study was to explore the origins of the chromosomes carrying the D178N mutation by designing a single-nucleotide polymorphism (SNP) haplotype around the PRNP gene. Haplotypes were constructed by genotyping six SNPs (rs2756271, rs13040327, rs6037932, rs13045348, rs6116474, and rs6116475) in 25 FFI patients from all over Spain. To augment the geographical scope of our study, 13 further FFI cases from Germany (9) and Italy (4) were also examined. Genotyping of SNPs in conjunction with the analysis of genealogical data for a group of FFI patients revealed the existence of two distinct haplotypes potentially associated with the D178N mutation. Of them, GCATTA-M proved to be the common haplotype of Spanish patients, whereas ACATTA-M was typical of the German cases. It is interesting to note that both haplotypes were identified in the Italian samples: GCATTA-M in a family from the Tuscany region and ACATTA-M in a family from the Veneto region. Our findings suggest the occurrence of two independent D178N-129M mutational events in Europe, preserved and transmitted from one generation to the next until nowadays. Likewise, results based on the analysis of SNP data indicate that previous hypotheses postulating that the D178N mutation had independent origins for each family and that its global distribution was determined by recurrent mutational events must be regarded with caution. [ABSTRACT FROM AUTHOR]