Biomedical subjects

S P Martynov

Publications and source records attributed to S P Martynov.

12 recordsLinked to original sources

PubMed2006

[Genealogical analysis of resistance to fusarium head blight in Russian and Ukrainian cultivars of common wheat Triticum aestivum L].

The GRIS3.5 information analytical system of wheat genetic resources was used to track the possible ways of the transmission of fusarium head blight resistance from ancestors to progenies in extended pedigrees of 149 Russian and Ukrainian cultivaris of winter common wheat. Analysis of variance was performed for the coefficient of parentage computed for the cultivars under study and the putative sources of resistance and revealed that groups of resistant and susceptible cultivars differed in the distribution of contributions of the sources. In the resistant group, significant results were obtained for the contributions of Odesskaya 16, Gostianum 237, and Frontana. Pedigree analysis showed that fusarium head blight resistance was most commonly transmitted from Gostianum 237 through Odesskaya 16 and its derivatives. The landrace Khar'kovskaya probably served as a source of resistance in the case of Gostianum 237. In addition, the set of resistance sources included Kooperatorka, Hope, San Pastore, Triticum timopheevii Zhuk., and Secale cereale. Some well-known sources of fusarium head blight resistance varying in genetic determinants--Sumai 3, Wangshuibai, Wuhan 1, Nyubay (China), Nobeokabozukomugi, Shinchunaga (Japan), Arina (Switzerland), Fundulea-201R (Romania), and Renan (France)--have so far not being employed in breeding in Russia and provide an important reserve for breeding for resistance.

Fusarium↗

PubMed2006

[Dynamics of genetic diversity in winter common wheat Triticum aestivum L. cultivars released in Russia from 1929 to 2005].

Genealogical analysis was used to study the dynamics of genetic diversity in Russian cultivars of winter common wheat from 1929 to 2005. The Shannon diversity index of the total set of released cultivars remained almost unchanged, although the number of original ancestors (landraces and genetic lines) increased almost tenfold in the period under study. This was explained in terms of the dependence of the modified Shannon diversity index on two parameters, the number of original ancestors and the mean coefficient of parentage. Significant direct effects were revealed: a positive effect of the former parameter and a negative of the latter. As a result, the increase in the number of original ancestors was compensated by the increase in relatedness of cultivars. Genetic erosion of realized diversity was observed, as a half of Russian landraces were lost. Although the mean coefficient of parentage did not reach its critical value (R = 0.25), cultivars of some regions (Central and Volga-Vyatka) proved to be closely related. A favorable gradual decrease in the mean coefficient of parentage was observed in the past 15 years. A set of modem winter wheat cultivars, which were introduced in the Russian State Catalog from 2002 to 2005, displayed a cluster structure. The overwhelming majority of cultivars formed two clusters originating from Bezostaya 1 (67% of cultivars) and Mironovskaya 808 (31%).

Genetic Variation↗

PubMed2005

[Analysis of genetic diversity of spring durum wheat (Triticum durum Desf.) cultivars released in Russia in 1929-2004].

Based on genealogical analysis, the genetic diversity of 78 spring durum wheat cultivars released in Russia in 1929-2004 have been examined. The temporal trends of change in diversity were studied using series of n x m matrices (where n is the number of the cultivars and m is the number of original ancestors) and calculating coefficients of parentage in sets of cultivars released in particular years. The pool of original ancestors of spring durum wheat cultivars includes 90 landraces and old varieties, more than a half (57%) of which originate from European countries, including Russia and Ukraine (45%). The original ancestors strongly differ in the frequency of presence in the cultivar pedigrees. Landraces Beloturka, Sivouska, Kubanka (T. durum Desf.), Transbaikalian emmer, Yaroslav emmer (T. dicoccum Schuebl.), Poltavka (T. aestivum L.), and the original ancestors of cultivars Kharkov 46, Narodnaya, and Melanopus 1932 enter in the pedigrees of more than half of cultivars created within the framework of various breeding programs. At that, their distribution by cultivars from different breeding centers strongly varies. Analysis of temporal dynamics of genetic diversity, based on genetic profiles and coefficients of parentage, has shown that the genetic diversity of Russian durum wheats increased during the period examined. Nevertheless, genetic erosion of the local material-a loss of approximately 20% of the pool of Russian original ancestors-has been found. The contribution of the original ancestors to the pedigrees of different cultivars, constructed in different breeding centers and recommended for cultivation in different regions, has been estimated. The variation of the released cultivars was highest in the Lower Volga region and lowest in the Ural region. In all, the lower threshold of genetic diversity in all regions does not reach the critical level, corresponding to the similarity of half-sibs. The set of modern cultivars included in the Russian Official List 2004 has a cluster structure.

Gene Frequency↗

PubMed2004

[Genealogic analysis of the resistance of winter wheat to common bunt].

Comparative genealogical analysis of North American (the United States and Canada) and Eastern European (Russia and Ukraine) winter wheat cultivars resistant and susceptible to common bunt has been performed. Analysis of variance applied to North American wheats has demonstrated that resistant and susceptible cultivars significantly differ from each other with respect to the contributions of common ancestors. The contributions of Oro (Bt4 and Bt7), Rio (Bt6), White Odessa (Bt1), and Florence (Bt3) to the resistant cultivars are significantly higher than their contributions to the susceptible ones. This demonstrates that the use of these resistance donors in wheat breeding for several decades has been effective. The contribution of PI-178383 (Bt8, Bt9, and Bt10) is considerably higher in the group of resistant cultivars bred after 1965. The mean contributions of Federation (Bt7) and Nebred (Bt4) are significantly higher in the group of resistant cultivars obtained before 1965; however, the differences in the contributions of these donors between new resistant and susceptible cultivars became nonsignificant. Among the Russian and Ukrainian cultivars, there are differences between groups of resistant and susceptible cultivars from different regions determined by the differences between the regional populations of the pathogen in racial composition. In the northern region, the contributions of the wheat grass (Agropyron glaucum) and the rye cultivar Eliseevskaya are significantly higher in the resistant cultivars; in the southern region, a local cultivar of the Odessa oblast is the prevalent resistant cultivar. In addition, cultivar Yaroslav Emmer is likely to be effective in the northern region; and foreign sources (Oro, Florence, Federation, and Triticum timopheevii), in the southern region. Very few sources of vertical resistance to common bunt are used for winter wheat breeding in Russia and Ukraine. The decrease in genetic diversity in favor of a few identical genes may cause adequate changes in the pathogen population and subsequent proliferation of the pathogen on the genetically identical substrate. A new interpretation of the resistance of line Lutescens 6028 as a source of new genes, Bt12 and Bt13, is suggested. Both genealogical and segregation analyses have shown that the genes determining the resistance of this line may be identical to those described earlier (Bt1, Bt3, Bt4, Bt6, and Bt7); and the high resistance of this line is determined by a combination of these genes.

Plant Diseases↗

PubMed2004

[Evaluation of polymorphism at microsatellite loci of spring durum wheat (Triticum durum Desf.) varieties and the use of SSR-based analysis in phylogenetic studies].

Polymorphism at 28 SSR loci was analyzed and described in 45 cultivars of spring durum wheat created in the former USSR and Russia during the last 80 years. Each cultivar was shown to have a unique allele combination. This allows SSR markers to be used to identify durum wheat varieties. Meanwhile, these markers can hardly be used to detect phylogenetic relationships among varieties and to specify their pedigrees, because genetic distances calculated on the basis of these markers do not correlate with the distance calculated by coefficient of parentage.

DNA, Plant↗

PubMed2004

[Trends in genetic diversity change of spring bread wheat cultivars released in Russia in 1929-2003].

Using genealogy analysis, we studied genetic diversity of 340 cultivars of spring bread wheat that were released on the territory of Russia in 1929-2003. Trends in the temporal change of genetic diversity were inferred from analysis of a set of n x m matrices, where n is the number of the released cultivars and m is the number of original ancestors. The pool of original ancestors of the spring bread wheat cultivars for the total period of study included 255 landraces, of which 88 were from the former USSR and modern Russia. The original ancestors showed great differences in their presence in the cultivar sets examined and, consequently, in their importance for the gene pool of Russian spring wheats. The distributions of contributions of dominant original ancestors to cultivar diversity were significantly different in different regions, indicating that the ancestors were specific for the cultivation conditions. During the last 75 years, the genetic diversity of the spring bread wheat cultivars has been increasing owing to the wide use of foreign material in Russian breeding programs. However, our analysis showed that about 60 landraces, including the Russian ones, were lost during the studied time period. The lost part makes up 35% of the gene pool of the Russian original ancestors. It is reasonable to assume that the lost landraces carried a gene complex f or adaptation to specific Russian environments. Specificity of the contributions of the original ancestors in the sets of cultivars produced in different breeding centers was established. A comparative analysis of genetic similarity of cultivars was carried out using coefficients of parentage. Significant differences in this parameter between breeding institutes and regions of cultivation were revealed.

Cluster Analysis↗

PubMed2003

[Genealogy-based comparative analysis of loose smut resistance of spring common wheat cultivars].

Comparative genealogical analysis was conducted for loose smut-resistant and susceptible common wheat cultivars of three regions: Russia, Canada, and India. Pedigree analysis of differentiator varieties revealed several sources of the Ut1, Ut3, and Ut4 genes. Tracking resistance transmission in extended pedigrees allowed identification of resistance donors, sources, and, in some cases, putative genes in Russian, Canadian, and Indian cultivars. A contingency table was constructed with the data on resistance or susceptibility of 839 common and durum wheat cultivars and demonstrated a significant association for resistance to two, loose and stinking, types of smut.

Basidiomycota↗

PubMed2003

[Genealogical approach to the formation of the winter wheat core collection].

The correctness of the genealogical approach to the estimation of genetic diversity has been substantiated. The approach implies a comparison of the estimates of similarity based on genetic markers and coefficients of parentage. A method of the application of the genealogical approach to the formation of the core collection has been developed. The adequacy of the core set has been estimated using Shannon's diversity index adapted for genetic profiles and the correlation between the distributions of ancestors' contributions. A core collection has been formed. This collection contains 25% of the accessions of the original winter wheat (Triticum aestivum L.) collection from the Czech Genebank and represents 70-76% of the intracluster diversity. A decrease in intercluster diversity has not been found in the core collection.

Botany↗

PubMed2003

[Evaluation of the relevance of using RAPD-analysis for revealing the phylogenic connections between cultivars of drum wheat (T. durum Desf.)].

A comparison of similarity indices between 64 durum wheat cultivars calculated using pedigree analysis and RAPD method showed a correspondence between these two approaches to estimation of genetic diversity. The associations between the results of RAPD clustering and coefficients of parentage (chi 2 test) and the coefficient of correlation between similarity matrices were statistically significant. However, the correlation was rather weak while pedigree analysis and RAPD method did not yield completely identical estimates of genetic diversity in the set of cultivars studied.

Phylogeny↗

PubMed2000

[Analysis of genetic diversity of wheat using genetic resources information system GRIS].

The possibilities of using the Genetic Resources Information and Analysis System (GRIS) 3.2, a database and software package, in studies of various aspects of genetic diversity in wheat are demonstrated. A model of genetic diversity was analyzed; diversity levels were estimated in wheat from various regions at different times. The genetic basis of Russian winter and spring common wheat cultivars was investigated. Transmission of powdery mildew resistance genes was traced in cultivars with identified Pm genes. For some genes, patterns of geographical distribution were characterized. Description of GRIS 3.2 is given: the package consists of a database on the global gene pool of wheat and software on genealogical and statistic analyses of genetic diversity.

Databases, Factual↗

PubMedDate not supplied

[Additional limitations of the Shrikhande method and their verification].

Shrikhande's method was checked on linear-variety common wheat Lutescens 62. Two causes for a distortion of the ratio of genotypic and paratypic components of the variance were established: parameter b of Smith's law is not constant for a given field and depends on the method of parcelling: Smith's law is not confirmed at all. A two-stage test of Shrikhande's method correctness is suggested for checking its limitations in practice. The analysis of variance for any given parcelling is done at the first stage. Significant ratios of between-cluster mean squares and within-cluster mean squares indicate that Smith's law is confirmed. The second stage consists in the analysis of variance of lg V(X) linear regression by lg X or in the graphical analysis of the function lg V(X) = = f (lg X).

Genetic Techniques↗

PubMedDate not supplied

[Evaluating the significance of differences between variants].

Experimental results of multiple comparisons for Tukey's, Newman-Kuels', Duncans' tests and for the t-test are compared. When the number of variants is more than two, the t-test is shown to reduce the value of the least significant difference, so that its use for multiple comparisons is incorrect. Duncan's multiple range test tends to increase the value of significant differences. The adequacy of Tukey's and Newman-Keuls' tests to the F-test is established.

Genetic Techniques↗