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1.
Plants (Basel) ; 13(3)2024 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-38337968

RESUMEN

Forest genetic conservation is typically species-specific and does not integrate interspecific interaction and community structure. It mainly focuses on the theories of population and quantitative genetics. This approach depicts the intraspecific patterns of population genetic structure derived from genetic markers and the genetic differentiation of adaptive quantitative traits in provenance trials. However, it neglects possible interspecific interaction in natural forests and overlooks natural hybridization or subspeciation. We propose that the genetic diversity of a given species in a forest community is shaped by both intraspecific population and interspecific community evolutionary processes, and expand the traditional forest genetic conservation concept under the community ecology framework. We show that a community-specific phylogeny derived from molecular markers would allow us to explore the genetic mechanisms of a tree species interacting with other resident species. It would also facilitate the exploration of a species' ecological role in forest community assembly and the taxonomic relationship of the species with other species specific to its resident forest community. Phylogenetic ß-diversity would assess the similarities and differences of a tree species across communities regarding ecological function, the strength of selection pressure, and the nature and extent of its interaction with other species. Our forest genetic conservation proposal that integrates intraspecific population and interspecific community genetic variations is suitable for conserving a taxonomic species complex and maintaining its evolutionary potential in natural forests. This provides complementary information to conventional population and quantitative genetics-based conservation strategies.

2.
Mol Ecol ; 17(10): 2463-75, 2008 May.
Artículo en Inglés | MEDLINE | ID: mdl-18430147

RESUMEN

The Canadian side of the Pacific Northwest was almost entirely covered by ice during the last glacial maximum, which has induced vicariance and genetic population structure for several plant and animal taxa. Lodgepole pine (Pinus contorta Dougl. ex. Loud.) has a wide latitudinal and longitudinal distribution in the Pacific Northwest. Our main objective was to identify relictual signatures of glacial vicariance in the population structure of the species and search for evidence of distinct glacial refugia in the Pacific Northwest. A maternally inherited mitochondrial DNA minisatellite-like marker was used to decipher haplotype diversity in 91 populations of lodgepole pine located across the natural range. Overall population differentiation was sizeable (G(ST) = 0.365 and R(ST) = 0.568). Four relatively homogeneous groups of populations, possibly representative of as many genetically distinct glacial populations, were identified for the two main subspecies, ssp. latifolia and ssp. contorta. For ssp. contorta, one glacial lineage is suggested to have been located at high latitudes and possibly off the coast of mainland British Columbia (BC), while the other is considered to have been located south of the ice sheet along the Pacific coast. For ssp. latifolia, two genetically distinct glacial populations probably occurred south of the ice sheet: in the area bounded by the Cascades and Rocky Mountains ranges, and on the eastern side of the Rockies. A possible fifth refugium located in the Yukon may have also been present for ssp. latifolia. Zones of contact between these ancestral lineages were also apparent in interior and northern BC. These results indicate the role of the Queen Charlotte Islands and the Alexander Archipelago as a refugial zone for some Pacific Northwest species and the vicariant role played by the Cascades and the American Rocky Mountains during glaciation.


Asunto(s)
ADN Mitocondrial/genética , ADN de Plantas/genética , Variación Genética , Pinus/genética , Colombia Británica , Haplotipos , Repeticiones de Minisatélite/genética , Filogenia , Quebec
3.
Sci Rep ; 7: 43178, 2017 02 22.
Artículo en Inglés | MEDLINE | ID: mdl-28225073

RESUMEN

Copy-number-variable (CNV) loci differ from single nucleotide polymorphic (SNP) sites in size, mutation rate, and mechanisms of maintenance in natural populations. It is therefore hypothesized that population genetic divergence at CNV loci will differ from that found at SNP sites. Here, we test this hypothesis by analysing 856 CNV loci from the genomes of 1184 healthy individuals from 11 HapMap populations with a wide range of ancestry. The results show that population genetic divergence at the CNV loci is generally more than three times lower than at genome-wide SNP sites. Populations generally exhibit very small genetic divergence (Gst = 0.05 ± 0.049). The smallest divergence is among African populations (Gst = 0.0081 ± 0.0025), with increased divergence among non-African populations (Gst = 0.0217 ± 0.0109) and then among African and non-African populations (Gst = 0.0324 ± 0.0064). Genetic diversity is high in African populations (~0.13), low in Asian populations (~0.11), and intermediate in the remaining 11 populations. Few significant linkage disequilibria (LDs) occur between the genome-wide CNV loci. Patterns of gametic and zygotic LDs indicate the absence of epistasis among CNV loci. Mutation rate is about twice as large as the migration rate in the non-African populations, suggesting that the high mutation rates play dominant roles in producing the low population genetic divergence at CNV loci.


Asunto(s)
Variaciones en el Número de Copia de ADN , Sitios Genéticos , Genética de Población , Tasa de Mutación , Epistasis Genética , Voluntarios Sanos , Humanos , Desequilibrio de Ligamiento , Grupos de Población
4.
Phytopathology ; 93(5): 633-9, 2003 May.
Artículo en Inglés | MEDLINE | ID: mdl-18942987

RESUMEN

ABSTRACT We have developed a new complementary model of gene interaction between diploid host and haploid pathogen by allowing for arbitrary levels of dominance in the host. This model enables us to assess the effects of overdominance, incomplete dominance, and underdominance on the equilibrium frequencies of resistance and virulence genes and on the stability of equilibria. Our model reduces to a gene-for-gene model when complete dominance of resistance is assumed. Computer simulations show that our model has two new features. First, when there is overdominance or underdominance of resistance, the internal equilibrium points exist even when there is no cost of unnecessary virulence or when there is a cost of necessary virulence at the balance between cost of unnecessary virulence and effectiveness of resistance. Second, the occurrence of stable resistance and virulence polymorphism is strongly dependent on the level of dominance. These two features suggest the need for caution when using the gene-for-gene model, especially in the presence of overdominance or underdominance. Our model is particularly suitable for studying the coevolutionary dynamics between hybrid populations and their pathogens in natural pathosystems.

5.
PLoS One ; 9(6): e100568, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24950065

RESUMEN

Hybrid zones as windows on evolutionary processes provide a natural laboratory for studying the genetic basis and mechanisms of postzygotic isolation. One resultant pattern in hybrid zones is the Hardy-Weinberg disequilibrium (HWD) for a single locus or the linkage disequilibrium (LD) for multiple loci produced by natural selection against hybrids. However, HWD and the commonly used low-order gametic or composite digenic LD cannot fully reflect the pattern of the high-order genotypic interactions. Here we propose the use of zygotic LD to elucidate the selection mechanisms of postzygotic isolation, and its calculation is based on genotypic frequencies only, irrespective of the type of mating system. We numerically and analytically show that the maximum composite digenic LD is always greater than the maximum absolute zygotic LD under the linear-additive selection, but is comparable to or smaller than the maximum absolute zygotic LD under the strong epistatic selection. Selection mechanisms can be inferred by testing such differences. We analyze a previously reported mouse hybrid zone assayed with genome-wide SNPs, and confirm that the composite digenic LD cannot appropriately indicate all possible significant genotypic interactions for a given SNP pair. A large proportion of significant zygotic LDs, ∼75% in general in the mouse hybrid zone, cannot be revealed from the composite digenic LD analysis. Statistical tests indicate that epistatic selection occurred among multiple loci in the mouse hybrid zone. The results highlight that the joint patterns of the composite digenic and zygotic LDs can help to elucidate the selection mechanism that is potentially involved in postzygotic isolation.


Asunto(s)
Fenómenos Ecológicos y Ambientales , Evolución Molecular , Hibridación Genética , Selección Genética , Cigoto , Animales , Femenino , Desequilibrio de Ligamiento , Masculino , Ratones , Modelos Biológicos , Probabilidad
6.
Ecol Evol ; 2(8): 1853-66, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22957188

RESUMEN

Jack pine (Pinus banksiana) and lodgepole pine (Pinus contorta var. latifolia) are two North American boreal hard pines that hybridize in their zone of contact in western Canada. The main objective of this study was to characterize their patterns of introgression resulting from past and recent gene flow, using cytoplasmic markers having maternal or paternal inheritance. Mitochondrial DNA (mtDNA) and chloroplast DNA (cpDNA) diversity was assessed in allopatric populations of each species and in stands from the current zone of contact containing morphological hybrids. Cluster analyses were used to identify genetic discontinuities among groups of populations. A canonical analysis was also conducted to detect putative associations among cytoplasmic DNA variation, tree morphology, and site ecological features. MtDNA introgression was extensive and asymmetric: it was detected in P. banksiana populations from the hybrid zone and from allopatric areas, but not in P. contorta populations. Very weak cpDNA introgression was observed, and only in P. banksiana populations. The mtDNA introgression pattern indicated that central Canada was first colonized by migrants from a P. contorta glacial population located west of the Rocky Mountains, before being replaced by P. banksiana migrating westward during the Holocene. In contrast, extensive pollen gene flow would have erased the cpDNA traces of this ancient presence of P. contorta. Additional evidence for this process was provided by the results of canonical analysis, which indicated that the current cpDNA background of trees reflected recent pollen gene flow from the surrounding dominant species rather than historical events that took place during the postglacial colonization.

7.
Curr Genomics ; 12(1): 55-70, 2011 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21886455

RESUMEN

An integration of the pattern of genome-wide inter-site associations with evolutionary forces is important for gaining insights into the genomic evolution in natural or artificial populations. Here, we assess the inter-site correlation blocks and their distributions along chromosomes. A correlation block is broadly termed as the DNA segment within which strong correlations exist between genetic diversities at any two sites. We bring together the population genetic structure and the genomic diversity structure that have been independently built on different scales and synthesize the existing theories and methods for characterizing genomic structure at the population level. We discuss how population structure could shape correlation blocks and their patterns within and between populations. Effects of evolutionary forces (selection, migration, genetic drift, and mutation) on the pattern of genome-wide correlation blocks are discussed. In eukaryote organisms, we briefly discuss the associations between the pattern of correlation blocks and genome assembly features in eukaryote organisms, including the impacts of multigene family, the perturbation of transposable elements, and the repetitive nongenic sequences and GC-rich isochores. Our reviews suggest that the observable pattern of correlation blocks can refine our understanding of the ecological and evolutionary processes underlying the genomic evolution at the population level.

8.
Theor Popul Biol ; 72(4): 547-59, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17905398

RESUMEN

The significance of migration load in driving the evolution of recipient populations has long been documented in population genetics, but its effects have not been linked to the formation of biased sex ratios in natural populations. In this study, we develop a single-locus model to demonstrate how the migration load can shape the primary and secondary sex ratios in dioecious plants where sexual dimorphism is determined by the sex chromosomes (the XX-XY or similar systems). Our results show that migration load can generate an array of sex ratios (from the female- to male-biased primary/secondary sex ratios), depending on the selection systems at the gametophyte and sporophyte stages and on the sex ratio in the migrating seeds. Ovule abortion and the purging of maladaptive genes from the immigrating pollen at the gametophyte stage can alter the primary sex ratio and indirectly alter the secondary sex ratio. The presence of maladaptive sex-linked genes from the migrating pollen and seeds of males facilitates the outcome of the female-biased secondary sex ratios, while the presence of maladaptive sex-linked genes from the migrating seeds of females can lead to the male-biased secondary sex ratios. The detrimental effects of the Y-chromosome from the migrating pollen and seeds can enhance the formation of female-biased primary and secondary sex ratios. These theoretical predictions highlight an alternative approach to the existing sex-ratio theories for interpreting the formation of biased sex ratios in the populations that are subject to the impacts of maladaptive genes from immigrants.


Asunto(s)
Emigración e Inmigración , Modelos Biológicos , Fenómenos Fisiológicos de las Plantas , Polinización , Razón de Masculinidad , Algoritmos , Semillas , Selección Genética
9.
Genome ; 48(3): 461-73, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16121243

RESUMEN

Noble fir (Abies procera Rehd) is a narrowly distributed conifer with a typical mainland-island structure of natural distribution. Here, we examined the genetic structure of populations native to the Pacific coast from Oregon to Washington (5 island and 16 mainland populations) with 14 polymorphic allozyme loci. A general method for estimating the number of unidirectional migrants from the mainland to island populations is presented in terms of the relation of average heterozygosity between the mainland and island populations. The results indicated that there were substantial island-mainland population differentiations (Fst = 0.107+/-0.029~0.154+/-0.039) but small differentiation within the mainland/submainland populations (0.037+/-0.008 approximately 0.054+/-0.010). Significant isolation by distance existed among the island-mainland populations and among the populations in Washington submainland. Four islands investigated received different numbers of migrants from the mainland/submainland. The southern island populations received a smaller number of migrants from the mainland but had greater genetic diversity, implying that there could be introgression with A. magnifica and (or) they represented possible glacial refuges and had expanded northwards after the last glaciations. The island populations close to the Pacific coast were more likely mainland-dependent.


Asunto(s)
Abies/genética , Genética de Población , Selección Genética , Alelos , Heterocigoto , Desequilibrio de Ligamiento , Oregon , Polimorfismo Genético , Washingtón
10.
Genome ; 45(3): 530-40, 2002 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-12033622

RESUMEN

We studied the population structure of a lodgepole (Pinus contorta Dougl.) and jack pine (Pinus banksiana Lamb.) complex in west central Alberta and neighboring areas by assessing random amplified polymorphic DNA (RAPD) variability in 23 lodgepole pine, 9 jack pine, and 8 putative hybrid populations. Of 200 random primers screened, 10 that amplified 39 sharp and reproducible RAPDs were chosen for the study. None of the 39 RAPDs were unique to the parental species. RAPD diversity ranged from 0.085 to 0.190 among populations and averaged 0.143 for lodgepole pine, 0.156 for jack pine, 0.152 for hybrids, and 0.148 for all 40 populations. The estimated population differentiation based on G(ST) was 0.168 for hybrids, 0.162 for lodgepole pine, 0.155 for jack pine, and 0.247 across all 40 populations. Cluster analysis of genetic distances generally separated jack pine from lodgepole pine and hybrids, but no division could be identified that further separated lodgepole pine from hybrids. The observed weak to mild trend of "introgression by distance" in the complex and neighbouring areas was consistent with the view that introgressive hybridization between lodgepole and jack pines within and outside the hybrid zone may have been through secondary contact and primary intergradation, respectively.


Asunto(s)
Variación Genética , Pinus/genética , Técnica del ADN Polimorfo Amplificado Aleatorio , Filogenia
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