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Selected AbstractsPhenotypic divergence but not genetic distance predicts assortative mating among species of a cichlid fish radiationJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 8 2009R. B. STELKENS Abstract The hypothesis of ecological divergence giving rise to premating isolation in the face of gene flow is controversial. However, this may be an important mechanism to explain the rapid multiplication of species during adaptive radiation following the colonization of a new environment when geographical barriers to gene flow are largely absent but underutilized niche space is abundant. Using cichlid fish, we tested the prediction of ecological speciation that the strength of premating isolation among species is predicted by phenotypic rather than genetic distance. We conducted mate choice experiments between three closely related, sympatric species of a recent radiation in Lake Mweru (Zambia/DRC) that differ in habitat use and phenotype, and a distantly related population from Lake Bangweulu that resembles one of the species in Lake Mweru. We found significant assortative mating among all closely related, sympatric species that differed phenotypically, but none between the distantly related allopatric populations of more similar phenotype. Phenotypic distance between species was a good predictor of the strength of premating isolation, suggesting that assortative mating can evolve rapidly in association with ecological divergence during adaptive radiation. Our data also reveals that distantly related allopatric populations that have not diverged phenotypically, may hybridize when coming into secondary contact, e.g. upon river capture because of diversion of drainage systems. [source] E2 quasispecies specificity of hepatitis C virus association with allografts immediately after liver transplantationLIVER TRANSPLANTATION, Issue 2 2004Michael G. Hughes Jr. It is unknown whether all hepatitis C virus (HCV) quasispecies variants found within patient serum have equal capacity to associate with the liver after transplantation; however, in vitro models of HCV infection suggest that variations in the hypervariable region 1 (HVR1) of the second envelope protein (E2) may be important in infectivity. The hypothesis of the current study is that the two hypervariable regions (HVR1 and HVR2) within E2 are important in the initial virus,liver interaction, and, therefore, certain HCV quasispecies variants will be isolated from the liver after reperfusion. In 8 patients with end-stage liver disease secondary to HCV infection, HCV envelope quasispecies were determined from intraoperative serum samples obtained before the anhepatic phase of transplantation and from liver biopsies 1.5 to 2.5 hours after the transplanted liver was perfused. Explanted (native) liver biopsies were taken as a control. Sequence analysis was performed on clones of specific HCV reverse transcriptase-polymerase chain reaction products spanning HVR1 and HVR2 of the E2 protein. HVR1 was more variable than HVR2 for all samples. Quasispecies isolated from postperfusion liver differed more from serum than did explanted liver quasispecies at HVR1 (P = 0.03) but not at HVR2 (P = 0.2). Comparison of HVR1 sequences from postperfusion liver versus serum revealed significantly less HVR1 genetic complexity and diversity (P = 0.02 and P = 0.04, respectively). Immediately after transplantation but before actual infection, liver allografts select out from the infecting serum inoculum a less heterogeneous, more closely related population of quasispecies variants. (Liver Transpl 2004;10:208,216.) [source] Does the relationship between IgE and the CD14 gene depend on ethnicity?ALLERGY, Issue 11 2008G. Zhang This review considers the data from studies analysing associations between the CD14C,159T single nucleotide polymorphism (SNP) and asthmatic phenotypes and discusses the variability of the conclusions. By searching PubMed and EMBASE for articles on CD14C,159T -related population or family-based association studies, 47 were identified up till September 2007. Collectively, the studies reviewed herein consistently showed population differences in frequencies of the alleles of the SNP, with African descent having the highest C allele frequencies, followed by Caucasians and Asians. The T allele of the SNP was associated with increased sCD14 in some studies but not in others. Inconsistently, the C allele, or even occasionally the T allele, was associated with atopic phenotypes in a population subgroup. There are several explanations for these inconsistencies, including lack of power, linkage disequilibrium, gene,gene interactions, population admixture and gene,environment interactions. If the SNP was associated with functional changes to the coded protein and thus modulating susceptibility to allergic disease, its effect may be modest and dependent on other co-existent, ethnicity-specific, genetic or environmental risk factors. [source] Genetic mapping of quantitative trait loci for resistance to Haemonchus contortus in sheepANIMAL GENETICS, Issue 3 2009K. Marshall Summary This paper presents results from a mapping experiment to detect quantitative trait loci (QTL) for resistance to Haemonchus contortus infestation in merino sheep. The primary trait analysed was faecal worm egg count in response to artificial challenge at 6 months of age. In the first stage of the experiment, whole genome linkage analysis was used for broad-scale mapping. The animal resource used was a designed flock comprising 571 individuals from four half-sib families. The average marker spacing was about 20 cM. For the primary trait, 11 QTL (as chromosomal/family combinations) were significant at the 5% chromosome-wide level, with allelic substitution effects of between 0.19 and 0.38 phenotypic standard deviation units. In general, these QTL did not have a significant effect on faecal worm egg count recorded at 13 months of age. In the second stage of the experiment, three promising regions (located on chromosomes 1, 3 and 4) were fine-mapped. This involved typing more closely spaced markers on individuals from the designed flock as well as an additional 495 individuals selected from a related population with a deeper pedigree. Analysis was performed using a linkage disequilibrium,linkage approach, under additive, dominant and multiple QTL models. Of these, the multiple QTL model resulted in the most refined QTL positions, with resolutions of <10 cM achieved for two regions. Because of the moderate size of effect of the QTL, and the apparent age and/or immune status specificity of the QTL, it is suggested that a panel of QTL will be required for significant genetic gains to be achieved within industry via marker-assisted selection. [source] Introduction Strategies Put to the Test: Local Adaptation versus HeterosisCONSERVATION BIOLOGY, Issue 3 2004PHILIPPINE VERGEER exogamia; introducciones multi-fuente; introducciones uni-fuente; Succisa pratensis Abstract:,Plant biodiversity has declined seriously because of both habitat deterioration and habitat fragmentation. As a result, many species have been forced into small, fragmented, and isolated populations and are believed to suffer from higher extinction risks. Genetic reinforcement and the establishment of new populations are now widely used to prevent extinction. However, the genetic background of transplants may seriously affect the long-term success of these populations because increased genetic variation may reduce the risk of inbreeding or lead to better performance by restored heterozygosity levels (heterosis). Introduced transplants, however, may be poorly adapted to the new local conditions. We tested the initial success of alternative introduction strategies. We evaluated the potential for inbreeding, heterosis, and/or local adaptation after introduction of artificial populations of Succisa pratensis. We introduced individuals from local and distant artificial populations that were created from either small or large populations. We created the artificial populations with the same census population size but varying effective population sizes by adjusting the relatedness of individuals. We analyzed the demographic consequences of inbreeding, heterosis, and/or local adaptation of these artificial populations. Reduced performance after selfing was manifested by a reduction in seed production, seed weight, germination, and flowering percentage. Seed production, seed weight, flowering percentage, and number of flowerheads were negatively affected by small population size. Local adaptation increased biomass and flowering percentage for local individuals. Seed weight and seed production exhibited significant heterosis. Our results demonstrate that threatened populations can benefit from introduction and genetic reinforcement of individuals from related populations. Significant differences among the artificial populations for several measured performance components suggest that introduction or reinforcement is best achieved through material from a local population or, when unavailable, from several large populations. Resumen:,La biodiversidad de plantas ha declinado seriamente tanto por el deterioro como la fragmentación de hábitats. Como resultado, muchas especies han sido relegadas a poblaciones pequeñas, fragmentadas y aisladas cuyos riesgos de extinción se piensa que son mayores. El reforzamiento genético y el establecimiento de poblaciones nuevas se utilizan ampliamente en la actualidad para prevenir la extinción. Sin embargo, los antecedentes genéticos de transplantes pueden afectar seriamente el éxito de estas poblaciones a largo plazo debido a que el incremento en la variación genética puede reducir el riesgo de endogamia o puede conducir a un mejor rendimiento por lograr niveles de heterocigosidad restaurados (heterosis). No obstante, los trasplantes introducidos pueden adaptarse deficientemente a las nuevas condiciones locales. Probamos el éxito inicial de estrategias de introducción alternativas. Evaluamos el potencial de endogamia, heterosis y/o adaptación local después de la introducción de poblaciones artificiales de Succisa pratensis. Introdujimos individuos de poblaciones locales y de poblaciones artificiales distantes que fueron creadas a partir de poblaciones tanto pequeñas como grandes. Las poblaciones artificiales fueron creadas con el mismo tamaño poblacional censal pero variaron en tamaños poblacionales efectivos al ajustar la parentela de los individuos. Analizamos las consecuencias demográficas de la endogamia, heterosis y/o adaptación local de estas poblaciones artificiales. Después de la autofecundación se manifestó una reducción en el rendimiento por reducción en la producción y peso de semillas y en el porcentaje de germinación y floración. La producción y peso de semillas, el porcentaje de floración y el número de botones florales fueron afectados negativamente por el tamaño poblacional pequeño. La adaptación local incrementó la biomasa y el porcentaje de floración en individuos locales. El peso y producción de semillas mostró heterosis significativa. Nuestros resultados demuestran que las poblaciones amenazadas pueden beneficiarse de la introducción y del reforzamiento genético de individuos de poblaciones emparentadas. Las diferencias significativas entre las poblaciones artificiales en varios de los componentes de rendimiento medidos sugiere que la introducción o reforzamiento se logra mejor con material de una población local o, cuando no disponible, con material de varias poblaciones grandes. [source] The peopling of Madeira archipelago (Portugal) according to HLA genesINTERNATIONAL JOURNAL OF IMMUNOGENETICS, Issue 1 2009A. Arnaiz-Villena Summary The Madeira-Porto Santo Archipelago was officially colonized in 1420 by Portuguese settlers. Its importance in Columbus' information for the American discovery and for slave traffic across the Atlantic is unquestionable. Thus, a complex peopling may have given rise to a present-day high admixture of ethnicities according to HLA genes. A sample of 173 healthy unrelated Madeirans was analysed and compared with 6986 HLA chromosomes from other worldwide populations. Genetic distances, neighbour-joining dendrograms and correspondence analyses were used for comparisons. Southern European, North African (including Canary Islands), Jewish and Mediterranean typical HLA alleles were found and genetic distances from Madeirans to these populations were the closest ones. In addition A*24-B*65-DRB1*0102-DQB1*0501 and A*68-B*08-DRB1*0301-DQB1*0201 haplotypes were newly found in Madeira and not found in any other population. Jewish-Armenian-Middle East haplotype (A*33-B*65-DRB1*0102-DQB1*0501) is one of the most common haplotypes; this haplotype is also present in Spaniards and North Africans. Quantitatively, Portuguese, North Africans (Algerians), Spaniards and Canary Islanders (in this order) are the most important parental populations to Madeirans. Results are discussed on the basis of the recorded historical peopling which does not show a noticeable African gene input in present-day Madeiran population according to our data; one of the closest related populations found is the Canary Islanders, suggesting that Guanche (Canary Islands first inhabitants) slaves gene flow is still noticed at present, both in Madeira and in Canary Islands populations. [source] Genetic restoration of a stocked brown trout Salmo trutta population using microsatellite DNA analysis of historical and contemporary samplesJOURNAL OF APPLIED ECOLOGY, Issue 4 2006MICHAEL M. HANSEN Summary 1Gene flow from domesticated to wild populations is a major threat to wild salmonid fish. However, few studies have addressed how populations could be restored after admixture has occurred. We analysed the prospects for restoring the previously intensively stocked brown trout population of the Skjern River, Denmark, by identifying remaining non-admixed individuals to be used for supportive breeding. 2We analysed microsatellite DNA markers in historical (1940,50s) and contemporary (1992,2004) samples from the Skjern River system, from the strain of domesticated trout previously used for stocking, and from the neighbouring Storå River. We analysed admixture proportions to estimate the genetic contribution by domesticated trout. We identified non-admixed trout using assignment tests, and further analysed the possible sources of indigenous trout by estimating contemporary migration among populations. 3Genetic differentiation between the historical Storå and Skjern river populations was low (,ST = 0·004), suggesting considerable gene flow in the past. The contemporary Skjern and Storå river populations and a supportive breeding brood stock were strongly admixed, but some non-admixed individuals nevertheless remained in the wild-caught samples. In addition, two resident populations in isolated tributaries were found to be indigenous. The indigenous anadromous individuals from the Skjern River were unlikely to have been recruited from either the isolated tributary populations or the neighbouring Storå River and were presumably derived from unidentified spawning sites in the river system. 4All but one non-admixed anadromous Skjern River trout were females, which we ascribed to sampling bias. Moreover, all non-admixed fish were late-spawning (January,February) whereas the majority of all trout caught for the study were ripe by November,December. The difference in spawning time could be an important factor delaying complete admixture of domesticated and indigenous trout. 5Synthesis and applications. This study demonstrates the feasibility of restoring populations that have been admixed with exogenous individuals, by identifying non-admixed individuals using genetic markers. However, the results also highlight the problem that numbers of identified non-admixed individuals may be small, necessitating identification of nearby, closely related populations that can be incorporated into breeding programmes. [source] Which cranial regions reflect molecular distances reliably in humans?AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 1 2009Evidence from three-dimensional morphology Knowledge of the degree to which various subsets of morphological data reflect molecular relationships is crucial for studies attempting to estimate genetic relationships from patterns of morphological variation. This study assessed the phylogenetic utility of six different human cranial regions, plus the entire cranium. Three-dimensional landmark data were collected for 83 landmarks from samples of skulls from 14 modern human populations. The data were subsequently divided into anatomical regions: basicranium, upper face, mandible, temporal bone, upper jaw, cranial vault, and a subset of points from around the entire cranium. Depictions of population molecular distances were calculated using published data on microsatellites for the same or closely related populations. Distances based on morphological variation of each of the anatomical regions were compared with molecular distances, and the correlations assessed. The morphology of the basicranium, temporal bone, upper face, and entire cranium demonstrated the highest correlations with molecular distances. The morphology of the mandible, upper jaw, and cranial vault, as measured here, were not significantly correlated with molecular distances. As the three-dimensional morphology of the temporal bone, upper face, basicranium, and entire cranium appear to consistently reflect genetic relationships in humans, especially with more reliability than the cranial vault, it would be preferable to focus on these regions when attempting to determine the genetic relationships of human specimens with no molecular data. Am. J.Hum. Biol., 2009. © 2008 Wiley-Liss, Inc. [source] New method to measure minisatellite variant repeat variation in population genetic studiesAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2002M. Brión The classical analysis of minisatellite variant repeat (MVR) variation using modular structures is limited by the lack of knowledge of the mutational process involved in the evolution of most of the minisatellites. In this study a new method to measure MVR variation and to calculate genetic distances using MVR codes is proposed. The method is based on the statistical similarity of MVR patterns and considers the complete variability of the minisatellite, enabling meaningful comparisons of closely related populations. As an example, the method has been applied to analyze variation in MSY1 (DYF155S1) in five sets of data from European and North African populations. Am. J. Hum. Biol. 14:421,428, 2002. [source] Similarities and distinctions in Y chromosome gene pool of Western SlavsAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 4 2010Marcin Wo, niak Abstract Analysis of Y chromosome Y-STRs has proven to be a useful tool in the field of population genetics, especially in the case of closely related populations. We collected DNA samples from 169 males of Czech origin, 80 males of Slovakian origin, and 142 males dwelling Northern Poland. We performed Y-STR analysis of 12 loci in the samples collected (PowerPlex Y system from Promega) and compared the Y chromosome haplotype frequencies between the populations investigated. Also, we used Y-STR data available from the literature for comparison purposes. We observed significant differences between Y chromosome pools of Czechs and Slovaks compared to other Slavic and European populations. At the same time we were able to point to a specific group of Y-STR haplotypes belonging to an R1a haplogroup that seems to be shared by Slavic populations dwelling in Central Europe. The observed Y chromosome diversity may be explained by taking into consideration archeological and historical data regarding early Slav migrations. Am J Phys Anthropol 142:540,548, 2010. © 2010 Wiley-Liss, Inc. [source] |