Differences In Genetic Control Research Articles

Genetics of immune response to Epstein-Barr virus: prospects for multiple sclerosis pathogenesis.

Epstein-Barr virus (EBV) infection has been advocated as a prerequisite for developing multiple sclerosis (MS) and possibly the propagation of the disease. However, the precise mechanisms for such influences are still unclear. A large-scale study investigating the host genetics of EBV serology and related clinical manifestations, such as infectious mononucleosis (IM), may help us better understand the role of EBV in MS pathogenesis. This study evaluates the host genetic factors that influence serological response against EBV and history of IM and cross-evaluates them with MS risk and genetic susceptibility in the Swedish population. Plasma IgG antibody levels against EBV nuclear antigen-1 (EBNA-1, truncated=aa[325-641], peptide=aa[385-420]) and viral capsid antigen p18 (VCAp18) were measured using bead-based multiplex serology for 8744 MS cases and 7229 population-matched controls. The MS risk association for high/low EBV antibody levels and history of IM was compared to relevant clinical measures along with sex, age at sampling, and associated HLA allele variants. Genome-wide and HLA allele association analyses were also performed to identify genetic risk factors for EBV antibody response and IM history. Higher antibody levels against VCAp18 (OR=1.74, 95% CI=1.60-1.88) and EBNA-1, particularly the peptide (OR=3.13, 95% CI=2.93-3.35), were associated with an increased risk for MS. The risk increased with higher anti-EBNA-1 IgG levels up to twelve times the reference risk. We also identified several independent HLA haplotypes associated with EBV serology overlapping with known MS risk alleles (e.g., DRB1*15:01). Although there were several candidates, no variants outside the HLA region reached genome-wide significance. Cumulative HLA risk for anti-EBNA-1 IgG levels, particularly the peptide fragment, was strongly associated with MS. In contrast, the genetic risk for high anti-VCAp18 IgG levels was not as strongly associated with MS risk. IM history was not associated with class II HLA genes but negatively associated with A*02:01, which is protective against MS. Our findings emphasize that the risk association between anti-EBNA-1 IgG levels and MS may be partly due to overlapping HLA associations. Additionally, the increasing MS risk with increasing anti-EBNA-1 levels would be consistent with a pathogenic role of the EBNA-1 immune response, perhaps through molecular mimicry. Given that high anti-EBNA-1 antibodies may reflect a poorly controlled T-cell defense against the virus, our findings would be consistent with DRB1*15:01 being a poor class II antigen in the immune defense against EBV. Lastly, the difference in genetic control of IM supports the independent roles of EBNA-1 and IM in MS susceptibility.

Quantitative trait loci, candidate genes, and breeding lines to improve salt tolerance at the flowering and seedling stages in rice

AbstractSalinity is a major environmental constraint that limits growth and productivity of rice all over the world. Although rice plants are vulnerable to salt stress at both seedling and flowering stages, genetic dissection of salt tolerance at the flowering stage is challenging due to non‐uniformity of stress application at the appropriate growth stage. The present study was conducted to identify quantitative trait loci (QTLs) and candidate genes associated with the flowering stage salt tolerance and compare with those associated with the seedling stage using a high‐resolution genetic map. A population of advanced generation introgression lines with uniform flowering time was evaluated for salt tolerance at the seedling and flowering stages. A genetic map was constructed using 14,230 polymorphic single nucleotide polymorphism markers between donor parents (TCCP and FL478) and the recurrent parent (RP) (Jupiter). Seventeen and 28 QTLs were identified for traits associated with salt tolerance at the seedling and flowering stage, respectively. Important candidate genes present in the flowering stage salt responsive QTL regions were OsHAK13, OsCYP21‐4, GIF1, and OsRGG20, whereas the seedling stage QTL intervals harbored genes such OsHAK20, STRK1, and OsMADS25. Gene expression analysis revealed upregulation of OsHAK13 and OsCYP21‐4 in TCCP, 3 days after exposure to salt stress at the flowering stage. Similarly, expression of OsHAK20, STRK1, and OsMADS25 was highly upregulated in TCCP under salt stress at the seedling stage. Due to differences in genetic control of salt tolerance at both seedling and flowering stages, stacking of genes/QTLs for salt tolerance at both stages will be needed. Since some beneficial QTLs were also contributed by the RP, emphasis should be on targeting the desirable QTLs from donors while retaining the beneficial QTLs of the RP to improve salinity tolerance in rice using marker‐assisted selection.

Seasonal Differences in Structural and Genetic Control of Digestibility in Perennial Ryegrass.

Perennial ryegrass is an important forage crop in dairy farming, either for grazing or haying purposes. To further optimise the forage use, this study focused on understanding forage digestibility in the two most important cuts of perennial ryegrass, the spring cut at heading and the autumn cut. In a highly diverse collection of 592 Lolium perenne genotypes, the organic matter digestibility (OMD) and underlying traits such as cell wall digestibility (NDFD) and cell wall components (cellulose, hemicellulose, and lignin) were investigated for 2 years. A high genotype × season interaction was found for OMD and NDFD, indicating differences in genetic control of these forage quality traits in spring versus autumn. OMD could be explained by both the quantity of cell wall content (NDF) and the quality of the cell wall content (NDFD). The variability in NDFD in spring was mainly explained by differences in hemicellulose. A 1% increase of the hemicellulose content in the cell wall (HC.NDF) resulted in an increase of 0.81% of NDFD. In autumn, it was mainly explained by the lignin content in the cell wall (ADL.NDF). A 0.1% decrease of ADL.NDF resulted in an increase of 0.41% of NDFD. The seasonal traits were highly heritable and showed a higher variation in autumn versus spring, indicating the potential to select for forage quality in the autumn cut. In a candidate gene association mapping approach, in which 503 genes involved in cell wall biogenesis, plant architecture, and phytohormone biosynthesis and signalling, identified significant quantitative trait loci (QTLs) which could explain from 29 to 52% of the phenotypic variance in the forage quality traits OMD and NDFD, with small effects of each marker taken individually (ranging from 1 to 7%). No identical QTLs were identified between seasons, but within a season, some QTLs were in common between digestibility traits and cell wall composition traits confirming the importance of hemicellulose concentration for spring digestibility and lignin concentration in NDF for autumn digestibility.

Genetic parameters for litter traits at different parities in purebred Landrace and Yorkshire pigs.

Comparison of the multi-trait animal model and the traditional repeatability model was carried out using data obtained from 6,424 Landrace and 20,835 Yorkshire sows farrowed from January 2000 to April 2018 in order to estimate genetic parameters for litter traits at different parities. Specifically, records of the total number born (TNB), number born alive (NBA), total number of mortality (MORT), number of stillborn (NSB) and number of mummified pigs (MUM) were used. Although results showed the heterogeneity of heritability for litter traits at different parities, the mean heritability estimates from the multi-trait model were found to be higher than those of the repeatability model for all traits in both pig breeds. In terms of genetic correlation between parities, a slight difference in genetic control in the first parity was noted for TNB and NBA in Landrace and Yorkshire pigs. The correlation between the first parity and later parities ranged from 0.48 to 0.74 for TNB and NBA in both breeds. Moreover, genetic correlation between parities for MORT and NSB was observed to be high for parities higher than 2 in Yorkshire pigs. For MUM, genetic correlation between the first and other parities was generally low in both breeds, indicating that culling pigs on the basis of MUM at the first parity could probably be unreasonable. Overall, the results of this study suggest that the multi-trait approach for litter size traits is useful for the accurate estimation of genetic parameters.

Genetic and hormonal control of hepatic steatosis in female and male mice

The etiology of nonalcoholic fatty liver disease is complex and influenced by factors such as obesity, insulin resistance, hyperlipidemia, and sex. We now report a study on sex difference in hepatic steatosis in the context of genetic variation using a population of inbred strains of mice. While male mice generally exhibited higher concentration of hepatic TG levels on a high-fat high-sucrose diet, sex differences showed extensive interaction with genetic variation. Differences in percentage body fat were the best predictor of hepatic steatosis among the strains and explained about 30% of the variation in both sexes. The difference in percent gonadal fat and HDL explained 9.6% and 6.7% of the difference in hepatic TGs between the sexes, respectively. Genome-wide association mapping of hepatic TG revealed some striking differences in genetic control of hepatic steatosis between females and males. Gonadectomy increased the hepatic TG to body fat percentage ratio among male, but not female, mice. Our data suggest that the difference between the sexes in hepatic TG can be partly explained by differences in body fat distribution, plasma HDL, and genetic regulation. Future studies are required to understand the molecular interactions between sex, genetics, and the environment.

Evaluation of Cowpea Genotypes for Resistance to <i>Fusarium redolens</i> in Uganda

Fusarium redolens, a virulent fungus which causes damping off, leaf yellowing, wilting and root rots has recently been devastating cowpea fields in Uganda. This study aimed at identifying cowpea genotypes that are resistant to Fusarium redolens. Therefore, ninety cowpea genotypes were evaluated two times against a highly virulent Fusarium redolens (isolate from Zombo in Paidha district) in the screen house in 2016. Genotype effect was highly significant (P 0.001) for root rot severity. Based on the Index of Susceptibility (IS), three genotypes (Asontem, Dan1 LA and IT89KD-88) remained resistant (IS 3.5) over the two screening periods, 72 moderately resistant (3.5 ≤ IS 6.5) and 11 susceptible (IS ≥ 6.5). Resistance was found to be enhanced by presence of lateral roots above or at the ground level. Further results suggested a difference in genetic control of resistance to root rots and seed rots caused by Fusarium redolens. All the released varieties tested (SECOW 1 T, SECOW 2 W, SECOW 3 B, SECOW 4 W and SECOW 5 T) had moderate resistance to Fusarium redolens. Correlation analysis revealed root rot severity was strongly correlated to disease incidence (+0.64, P 0.001), to proportion of plants with lateral roots (-0.56, P 0.001), to amount of leaf chlorophyll (-0.53, P 0.001) and to proportion of plants that died prematurely due to Fusarium redolens infection (+0.45, P 0.001). No significant correlation was detected between root rot severity and proportion of plants that germinated. The established resistance could be exploited for improvement of farmer preferred cowpea varieties towards Fusarium redolens resistance in Uganda.

The autosomal genetic control of sexually dimorphic traits in humans is largely the same across the sexes.

There are substantial phenotypic differences between the male and female human. Several complex traits have recently been tested to see whether these phenotypic differences are explained by differences in genetic control between males and females. While some differences in genetic control between males and females are detected, overall the results demonstrate that the genetic control of complex traits in humans is largely the same across the sexes.Please see related Research article: http://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-1025-x

Latitudinal variation in sensitivity of flower bud formation to high temperature in Japanese Taraxacum officinale

Control of flowering time plays a key role in the successful range expansion of plants. Taraxacum officinale has expanded throughout Japan during the 110years after it was introduced into a cool temperate region. The present study tested a hypothesis that there is a genetic difference in the bud formation time in relation to temperature along latitudinal gradient of T. officinale populations. In Experiment 1, plants from three populations at different latitudes (26, 36, and 43°N) were grown at three temperatures. Time to flower bud appearance did not significantly differ among the three populations when plants were grown at 14°C, whereas it increased with increasing latitude when grown at 19 and 24°C. Rosette diameter was not different among the populations, indicating that the variation in bud formation time reflected a difference in genetic control rather than size variation. The latitudinal variation in bud appearance time was confirmed by Experiment 2 in which plants from 17 population were used. In Experiment 3, the size of plants that exhibited late-flowering was studied to test a hypothesis that the variation in flowering time reflects dormancy of vegetative growth, but the late-flowering plants were found to continue growth, indicating that vegetative dormancy was not the cause of the variation. The results clearly indicate that the degree of suppression of flower bud formation at high temperature decreases with latitude from north to south, which is under genetic control.

Greenbug resistance in barley accessions from East and South Asia

Heterogeneous forms differing in level of expressing resistance to the Krasnodar greenbug population have been revealed as a result of studying 1358 barley accessions from East and South Asian countries. High resistance of 98 accessions is controlled by alleles not identical to alleles of the earlier identified Rsg1 gene. A difference in genetic control of resistance in barley landraces from China and North Korea was found.

Late‐Acting Self‐Incompatibility inIpomopsis tenuifolia(Gray) V. Grant (Polemoniaceae)

Several different self‐incompatibility (SI) syndromes have been previously reported from Polemoniaceae, including differences in genetic control, timing of the response, and the location of pollen tube inhibition. In order to examine the evolutionary linkage between genetic control and site of pollen tube inhibition, crossing experiments and microscopic analyses were performed on an additional species of Polemoniaceae, Ipomopsis tenuifolia. Thirteen individuals from a natural population were used for the parental crosses; three F1 full‐sibling arrays were grown to maturity. Strong self‐incompatibility was found in the parental population on the basis of significant differences in the percentages of seed set in self‐ versus outcross matings. In the F1 arrays, none of the outcrosses or backcrosses was completely incompatible, leading to a large number of mating types. On the basis of the number of mating types in the F1 arrays, self‐recognition in this species must be based on full allelic matching of at least three loci. Pollen tubes were observed inside the ovary after both cross‐ and self‐pollination using SEM and fluorescent microscopy, suggesting that self‐pollination recognition takes place in the ovule, representing a late‐acting SI system. The large number of different SI mechanisms reported in the Polemoniaceae suggest that this family may be particularly labile in its breeding system.

Expression of Dlx genes during the development of the zebrafish pharyngeal dentition: evolutionary implications

In order to investigate similarities and differences in genetic control of development among teeth within and between species, we determined the expression pattern of all eight Dlx genes of the zebrafish during development of the pharyngeal dentition and compared these data with that reported for mouse molar tooth development. We found that (i) dlx1a and dlx6a are not expressed in teeth, in contrast to their murine orthologs, Dlx1 and Dlx6; (ii) the expression of the six other zebrafish Dlx genes overlaps in time and space, particularly during early morphogenesis; (iii) teeth in different locations and generations within the zebrafish dentition differ in the number of genes expressed; (iv) expression similarities and differences between zebrafish Dlx genes do not clearly follow phylogenetic and linkage relationships; and (v) similarities and differences exist in the expression of zebrafish and mouse Dlx orthologs. Taken together, these results indicate that the Dlx gene family, despite having been involved in vertebrate tooth development for over 400 million years, has undergone extensive diversification of expression of individual genes both within and between dentitions. The latter type of difference may reflect the highly specialized dentition of the mouse relative to that of the zebrafish, and/or genome duplication in the zebrafish lineage facilitating a redistribution of Dlx gene function during odontogenesis.

Comparison of QTLs for Early Elongation Ability between Two Floating Rice Cultivars with a Different Phylogenetic Origin

The ability to initiate stem elongation at the early growth stages of a plant is the major survival mechanism of floating rice in the presence of flooding. We previously identified two quantitative trait loci (QTLs) for this “early elongation ability” on chromosomes 3 and 12 using a Patnai23 (a non-floating cultivar) × Goai (a floating cultivar) F2 population. The objectives of the present study were: (1) to identify QTLs for early elongation ability in the cross Habiganj Aman VIII (a floating cultivar) × Patnai23, and (2) to confirm the results obtained in our previous diallel analysis indicating that Habiganj Aman VIII might harbour additional gene(s) for early elongation ability compared with Goai. The genotype of a total of 192 F2 plants was investigated using 85 (9 RFLP and 76 SSR) markers and the plants were assessed for early elongation ability. We scaled early elongation ability based on the position of the lowermost internode that exhibited elongation (“lowest elongated internode”, LEI), since the LEI position parallels the time of the onset of stem elongation. As a result, a large QTL detected on chromosome 12 seemed to be common to the two crosses. A small QTL detected on chromosome 1 was unique to the Habiganj Aman VIII × Patnai23 cross, which was consistent with the results obtained in our previous diallel analysis. No QTLs were found on chromosome 3 in this cross. These results suggested that (1) the QTL on chromosome 12 might be the most important one for the expression of early elongation ability in terms of the to percentage of phenotypic variation and consistency in different backgrounds, and (2) diallel analysis might be an effective method for examining differences in genetic control among diverse parents.

Site and gender specificity of inheritance of bone mineral density.

Differences in genetic control of BMD by skeletal sites and genders were examined by complex segregation analysis in 816 members of 147 families with probands with extreme low BMD. Spine BMD correlated more strongly in male-male comparisons and hip BMD in female-female comparisons, consistent with gender- and site-specificity of BMD heritability. Evidence from studies in animals and humans suggests that the genetic control of bone mineral density (BMD) may differ at different skeletal sites and between genders. This question has important implications for the design and interpretation of genetic studies of osteoporosis. We examined the genetic profile of 147 families with 816 individuals recruited through probands with extreme low BMD (T-score < -2.5, Z-score < -2.0). Complex segregation analysis was performed using the Pedigree Analysis Package. BMD was measured by DXA at both lumbar spine (L1-L4) and femoral neck. Complex segregation analysis excluded purely monogenic and environmental models of segregation of lumbar spine and femoral neck BMD in these families. Pure polygenic models were excluded at the lumbar spine when menopausal status was considered as a covariate, but not at the femoral neck. Mendelian models with a residual polygenic component were not excluded. These models were consistent with the presence of a rare Mendelian genotype of prevalence 3-19%, causing high BMD at the hip and spine in these families, with additional polygenic effects. Total heritability range at the lumbar spine was 61-67% and at the femoral neck was 44-67%. Significant differences in correlation of femoral neck and lumbar spine BMD were observed between male and female relative pairs, with male-male comparisons exhibiting stronger lumbar spine BMD correlation than femoral neck, and female-female comparisons having greater femoral neck BMD correlation than lumbar spine. These findings remained true for parent-offspring correlations when menopausal status was taken into account. The recurrence risk ratio for siblings of probands of a Z-score < -2.0 was 5.4 at the lumbar spine and 5.9 at the femoral neck. These findings support gender- and site-specificity of the inheritance of BMD. These results should be considered in the design and interpretation of genetic studies of osteoporosis.

Genetic control of colour/pattern polymorphism in British populations of the spittlebug Philaenus spumarius (L.) (Homoptera: Aphrophoridae)

The results of breeding experiments designed to determine the genetic control of the colour/pattern polymorphism in Philaenus spumarius in certain British populations are described and contrasted to previously published results for material taken from populations in southern Finland. The 11 principal phenotypes are controlled by seven alleles at a single autosomal locus, with complex patterns of dominance and co-dominance. In Finland, and most of the rest of the species' extensive range, the eight melanic morphs are wholly or substantially limited to the females, in which they are dominant to the typical form. Previously, this sex limitation has been explained in terms of reduced penetrance of melanic alleles in males and/or dominance reversal between the sexes, such that the eight melanic phenotypes (controlled by five alleles which are adjacent in the dominance heirarchy) are dominant to typical in the females but recessive in the males. Published data on morph frequencies in S Finland and on breeding experiments using material collected from these populations are re-examined and it is shown that neither theory accounts adequately for all the evidence. By contrast, in most British populations there is greatly increased penetrance in males of the melanic morphs which are strictly female-limited elsewhere. Breeding experiments, using P. spumarius taken from selected British populations, provide clear evidence that melanics are dominant to typical in both sexes. This difference in genetic control is entirely consistent with the balance of morph frequencies between the sexes in the populations from which the breeding material for the two separate studies was taken. Experimental material for this study was taken from populations in the Cynon Valley in south Wales, which have the highest melanic frequencies in the species' range and show particularly clear expression of melanic phenotypes in males. Both of these features are strongly correlated with severe aerial pollution from a local smokeless fuel factory. Selection for melanism in these populations is clearly strong, which probably accounts for the high level of penetrance and the dominance of melanics to typical in both sexes. Although further experiments are needed, it is suggested that regulatory loci, controlling the penetrance and expression of melanic alleles in males, could account for the observed differences in genetic control between populations in Britain and Finland.