RESUMO
Identifying the genetic basis of parallelism reveals the means by which evolution repeats itself and shows what aspects-if any-may be predictable. The recently tetraploid luteus group of Mimulus contains five species native to central Chile, three of which have evolved extensive red floral pigmentation using at least two distinct loci . Here we show that the parallel evolution of petal lobe anthocyanin (PLA) pigmentation in M. cupreus and M. luteus var. variegatus occurred via separate yet strikingly similar mechanisms. In each case, a dominant, single-locus gain of pigmentation maps to a genomic region (pla1 and pla2, respectively) containing adjacent, apparently recently duplicated paralogs of MYB anthocyanin-regulating transcription factors. Interestingly, candidate genes in pla1 and pla2 are themselves related by an older duplication. In both cases, pla genotype cosegregates with expression of multiple genes in the anthocyanin biosynthetic pathway, revealing a mechanism of coordinated trans-regulatory expression changes across functionally related enzyme-encoding genes. We conclude that in this instance, evolution has repeated itself with marked consistency. Duplication has enabled that repetition to occur using two physically independent but functionally similar loci, highlighting the importance of genomic complexity to the evolutionary process.
Assuntos
Evolução Biológica , Flores/genética , Duplicação Gênica , Mimulus/genética , Pigmentação , Antocianinas/química , Antocianinas/genética , Chile , Cromossomos de Plantas/genética , Flores/química , Regulação da Expressão Gênica , Mimulus/química , Especificidade da Espécie , Tetraploidia , Fatores de Transcrição/genéticaRESUMO
Deciphering the genetic architecture of phenotypic change provides a framework for understanding how evolution proceeds at a genetic level, and paves the way for work at the molecular level. A series of intra- and interspecific crosses were used to investigate the genetic control of recently evolved floral pigmentation phenotypes in a group of closely related Mimulus species from central Chile. An intraspecific polymorphism was found to be controlled by a single Mendelian locus. Differences between species, by contrast, were composed of multiple independent patterning elements, including both Mendelian and polygenic traits. The most striking phenotypic novelty in this group, anthocyanin pigmentation in the petal lobes, has evolved three times independently. The results illustrate how genetically simple modular elements can interact with polygenic or quantitative traits to create complex new phenotypes. The repeated evolution of petal lobe anthocyanins suggests that natural selection may have played a role in the evolution of red coloration in the Chilean Mimulus, and shows that red coloration has been achieved via different genetic pathways in these closely related species.
Assuntos
Evolução Biológica , Flores/genética , Variação Genética , Mimulus/genética , Pigmentação/genética , Antocianinas , Padronização Corporal/genética , Chile , Segregação de Cromossomos/genética , Cromossomos de Plantas/genética , Cruzamentos Genéticos , Hibridização Genética , Luz , Fenótipo , Polimorfismo Genético , Locos de Características Quantitativas/genética , Característica Quantitativa Herdável , Sementes/genética , Especificidade da EspécieRESUMO
Divergent populations are intrinsically reproductively isolated when hybrids between them either fail to develop properly or do not produce viable offspring. Intrinsic isolation may result from Dobzhansky-Muller (DM) incompatibilities, in which deleterious interactions among genes or gene products lead to developmental problems or underdominant chromosome structure differences between the parents. These mechanisms can be tested by studying marker segregation patterns in a hybrid mapping population. Here we examine the genetic basis of abnormal development in hybrids between two geographically distant populations of the moss Ceratodon purpureus. Approximately half of the hybrid progeny exhibited a severely reduced growth rate in early gametophyte development. We identified four unlinked quantitative trait loci (QTL) that interacted asymmetrically to cause the abnormal development phenotype. This pattern is consistent with DM interactions. We also found an excess of recombination between three marker pairs in the abnormally developing progeny, relative to that estimated in the normal progeny. This suggests that structural differences in these regions contribute to hybrid breakdown. Two QTL coincided with inferred structural differences, consistent with recent theory suggesting that rearrangements may harbor population divergence alleles. These observations suggest that multiple complex genetic factors contribute to divergence among populations of C. purpureus.
Assuntos
Bryopsida/crescimento & desenvolvimento , Bryopsida/genética , Hibridização Genética , Segregação de Cromossomos , Cruzamentos Genéticos , Equador , Marcadores Genéticos , Escore Lod , Modelos Genéticos , Locos de Características Quantitativas , Recombinação GenéticaRESUMO
We report the construction of a linkage map for the moss Ceratodon purpureus (n = 13), based on a cross between geographically distant populations, and provide the first experimental confirmation of maternal chloroplast inheritance in bryophytes. From a mapping population of 288 recombinant haploid gametophytes, genotyped at 121 polymorphic AFLP loci, three gene-based nuclear loci, one chloroplast marker, and sex, we resolved 15 linkage groups resulting in a map length of approximately 730 cM. We estimate that the map covers more than three-quarters of the C. purpureus genome. Approximately 35% of the loci were sex linked, not including those in recombining pseudoautosomal regions. Nearly 45% of the loci exhibited significant segregation distortion (alpha = 0.05). Several pairs of unlinked distorted loci showed significant deviations from multiplicative genotypic frequencies, suggesting that distortion arises from genetic interactions among loci. The distorted autosomal loci all exhibited an excess of the maternal allele, suggesting that these interactions may involve nuclear-cytoplasmic factors. The sex ratio of the progeny was significantly male biased, and the pattern of nonrandom associations among loci indicates that this results from interactions between the sex chromosomes. These results suggest that even in interpopulation crosses, multiple mechanisms act to influence segregation ratios.