Identification and certification of Bactrian and Arvan camels of Kazakh population using DNA technology// FUNDAMENTAL AND APPLIED SCIENTIFIC RESEARCH: сб.науч.тр./ OEAPS Inc.; редкол.: Флора Бертран (отв.ред.) [и др.]. - Берлин, Германия : OEAPS Inc., 2018. - С. 44-56.

2018 ◽  
Author(s):  
Elmira Kalybaevna Adil’bekova ◽  
Nuradin Alibaev ◽  
Arunas Svitojus

Kazakhstan is the center where Bactrians and Dromedaries can be raised, and hybridization between them has become widespread. Genetic resources of interspecies camel hybrids, raised in Kazakhstan, are represented by 30 generations.The most highly valuable in the conditions of Central Asia and Kazakhstan are transboundary camel breeds such as Kazakh Bactrian, Turkmen and Kazakh Dromedary, as well as new generations of camels Arada, Bainar and Baitur.At pure breeding of Kazakh Bactrian, genetic peculiarities are not taken into account, in view of the poor knowledge of this issue. To maintain the biodiversity, molecular genetic monitoring of the state of camel populations is required. Cytogenetic monitoring and certification are one of the promising areas for reliable camel genome assessment.Deep determination of Kazakh dairy camelsallele poolwas not carried out in Kazakhstan before. Genetic studies to optimize structure, identification and certification of valuable genotypes, as well as systematization of genetic resources in dairy camel breeding in Kazakhstan are urgent task.The aim of the study is identification, systematization and certification of genetic resources of Bactrian and Dromedary camels of Kazakh population using DNA technology. Genetic analysis of the typing results of the camels studied was carried out by 7 and 8 loci of DNA microsatellites. The material for the studies was DNA samples isolated from histological samples. The microsatellite loci were selected in accordance with the recommendations of the European Society of Genetics (FAO/ISAG).Identification and certification of Arvan and Kazakh Bactrian camels’ genetic resources using the microsatellite analysis of their genotype was carried outfor the first time. Breeding significance of Bactrian and Arvan camels of Kazakh population using DNA technologies was studied and determined. The obtained results of the study allowed evaluate camels at the level of the allelic profile.

Pathogens ◽  
2021 ◽  
Vol 10 (11) ◽  
pp. 1473
Author(s):  
Nikolaus Helmer ◽  
Hubert Blatterer ◽  
Christoph Hörweg ◽  
Susanne Reier ◽  
Helmut Sattmann ◽  
...  

Several species of avian schistosomes are known to cause dermatitis in humans worldwide. In Europe, this applies above all to species of the genus Trichobilharzia. For Austria, a lot of data are available on cercarial dermatitis and on the occurrence of Trichobilharzia, yet species identification of trematodes in most cases is doubtful due to the challenging morphological determination of cercariae. During a survey of trematodes in freshwater snails, we were able to detect a species in the snail Physella acuta (Draparnaud, 1805) hitherto unknown for Austria, Trichobilharzia physellae; this is also the first time this species has been reported in Europe. Species identification was performed by integrative taxonomy combining morphological investigations with molecular genetic analyses. The results show a very close relationship between the parasite found in Austria and North American specimens (similarity found in CO1 ≥99.57%). Therefore, a recent introduction of T. physellae into Europe can be assumed.


2017 ◽  
Vol 54 ◽  
pp. 216-221 ◽  
Author(s):  
Yu. V. Gyzieev ◽  
О. V. Sydorenko ◽  
L. V. Vishnevsky

In Ukraine, especially in certain natural and climatic zones, an important role in the production of food and social life of the population is played by the Carpathian Brown breed of cattle that extremely efficiently uses the natural pastures of the Carpathians. Animals of this breed have unique biological characteristics, resistant to diseases, have high resistance, the ability to withstand stress, have a strong constitution, a high duration of productive use, reproductive and adaptive ability, the content of protein in milk, available for chewing the kappa-casein fraction, good parameters for realization of genetic potential. The Carpathian Brown cattle with its high adaptability to the environment deserve the preservation and sustainable use, and for this purpose it is necessary to create a reliable genetic foundation. Moreover, it is important to know the genetic features of animals that are intended to produce specific products and still remain a significant functional element of the production system in the region. The gene kappa-casein is one of the few known genes, is uniquely associated with the signs of protein digestibility and technological properties of milk. Allele In the kappa-casein gene is associated with a higher protein content in milk, a higher yield of cheese, as well as better coagulation properties of milk. The purpose of this work was to establish the genotypes and to determine the genetic structure of the population of the Carpathian Brown breeders for the gene of kappa-casein (CSN3) with the determination of the possibility of their further use. The material for research was the semen of the bulls of Carpathian Brown breed (n = 21 heads), which originate from the leading tribal herds of the Zakarpattia oblast and evaluated by origin, by their own productivity at the Zakarpattia Regional State Tribal Station (now Private Joint-stock company "Zakarpatske plempidpryyemstvo"). In accordance with FAO recommendations for assessing the risk status of animal genetic resources and calculations carried out, a brown Carpathian breed of cattle is in the critical state of risk of disappearance. This status depends on the effective size of the population, the number of females and males, trends in the dynamics of their changes and the way breeder breeding work. In 2005 in 16 controllable herds of Zakarpattia and Ivano-Frankivsk oblasts there were 2866 heads of cattle of Carpathian Brown breed, including 1083 cows. And since 2014 according to the State Register of subjects of breeding business in livestock breeding, no breeding farm has left in Ukraine for breeding this kind of breed and there is no program of breeding the pedigrees. The breeding stock of Carpathian Brown breed is breeding only in private peasant farms. According to FAO recommendations, a part of the genetic material from the breeders of the brown Carpathian breed that belongs to Private Joint-stock company "Zakarpatske plempidpryyemstvo" was deposited in the Bank of Animals of Genetic Resources of Institute of Animal Breeding and Genetics nd. a. M.V.Zubets of NAAS. According to the data provided in the section "Reserve gene pool" of the Catalog of bulls of dairy and dairy-meat breeds, allowed to reproduce the mother stock in 2017, information is provided on 28 bulls of Carpathian Brown breed with available semen. Therefore, taking into account the results of the monitoring and analysis carried out, it should be noted that the possibility of restoration of the stock breed stock of Carpathian Brown breed has not been lost. Carpathian Brown breed as a local breed requires systematic population-genetic monitoring. The genetic material of the breeders of Carpathian Brown breed according to the genealogical structure is diverse and belongs to 12 lines. The most numerous representatives of the fruit of the lines of the Sokola 553 i Malchyka 3, Kaplera 43, Stretcha 143612, Fitsko 33, Pishty 10, Eleyma 110327, Raneta 584, Rupora 6507, Siroho 1759, Shoni 6 i Yu. Yuvelira 273, which at one time were the most widespread in the breed. Representatives of these lines for the CSN3 gene revealed polymorphism of all possible variants of the genotypes AA, AB and BB. According to the results of molecular genetic analysis, determination of frequency of distribution of genotypes and alleles of bulls of Carpathian Brown breed according to the gene of kapa-casein CSN3 has been determined. The frequency of the desired genotype BB among the examined animals was 0.143, and the frequency of carriers of the genotype AA was 0.381. Frequency of carriers of the heterozygous genotype AB was 0.476. The carrier frequency of the allele A in the animals tested is 0.619, which is twice as high as the allele B frequency of 0.381. By Hardy-Weinberg law, we did not determine the probable difference between the actual and expected distribution of genotype frequencies for the CSN3 gene. Conclusions on the basis of the analysis of the established genotypes and the determined frequency of allelic variants for the kappa-casein (CSN3) gene in the explored bogs of Carpathian Brown breed Private Joint-stock company "Zakarpatske plempidpryyemstvo" it was revealed that the available genetic resources of the pedigrees are quite varied according to the genealogical and genetic structure.


Author(s):  
S. Kamyshov ◽  
K. Izrailbekova

In the last decade, in the field of oncology, there has been an increasing interest in the study of issues related to the problem of primary multiple malignant tumors (PMMT). Many researchers agree that polyneoplasias are most often found in women, which is associated with an increase in the incidence of hormone-dependent tumors of the reproductive system, which is functionally represented by the mammary glands, uterus and ovaries. The development of comprehensive examination methods, including molecular genetic studies, contributes to the identification of synchronous PMMT of the female reproductive system. In our studies, metachronous tumors prevailed among PMMTs in breast cancer (65.7%). The most common metachronous cancer of the uterine body (37.1% of cases). Determination of the level of specific tumor markers allows you to monitor in advance the development of PMMT in this category of patients. Thus, each of the tumors of the female reproductive system should be considered as an indicator of the risk of the others, which should lead to a state of rapid response to the entire well-functioning system of dispensary registration, observation and use of a full range of special methods of clarifying diagnostics.


Author(s):  
P. A. Kosachev

<span lang="EN-US">The system and conspectus of the genus <em>Pedicularis</em> </span><span lang="EN-US">L. (Orobanchaceae) of </span><span lang="EN-US">Altai and Tien Shan is presented. The system is based of molecular genetic studies of the genus (Ree, 2005; Tkach et al., 2014; own data) and is represented by series that are grouped into sections. The b</span><span lang="EN-US">uilding</span><span lang="EN-US"> </span><span lang="EN-US">of the higher taxonomic categories is not possible at the moment due to the para- </span><span lang="EN-US">or polyphyletic</span><span lang="EN-US"> </span><span lang="EN-US">origin genus of weak support for clads in the phylogenetic tree. Conspectus includes 61 species of the 32 series and 7 sections. 16 species and 1 subspecies of endemic for the territory of the Altai and Tien Shan. For the first time described in one section and 10 series. Three sections published of the lectotypes: <em>Schizocalyx</em> Li, <em>Botryantha</em> Li, <em>Rhizophyllum</em> Li. Clarified the amount and distribution of species, series, sections. Displaying Altai and Tien Shan origin some series (ser. <em>Abrotanifoliae, Amoenae, Achilleifolia, Uliginosae, Physocalyces, Macrochilae, Platyrhynchae</em>), the Tien-Shan (<em>Semenowianae, Pycnanthae, Maximowiczianae, Pubiflorae</em>), Altai (<em>Brachystaches, Elatae</em>).</span>


2021 ◽  
Vol 9 (3) ◽  
pp. 481-491
Author(s):  
T.M. Cherdantseva ◽  
◽  
O.V. Bakovetskaya ◽  
A.A. Nikiforov ◽  
M.S. Nekrasovа ◽  
...  

Muscular dystrophies are one of the most pressing problems of modern medicine. In the electronic library system e-Library on the topic “Muscular Dystrophies” 13,263 papers have been published, over the past 5 years — 4,221, and in PubMed, at the request of “Muscular Dystrophy”, more than 37 thousand publications have been found, over the past 5 years there are about 6,851. The interest in this problem is understandable, since the prevalence of progressive muscular dystrophies is 200 cases per 1 000,000 population, which permits to classify them as the most common forms of hereditary pathology. The article provides an overview of information on morphological and laboratory genetic. CONCLUSION: The literature review showed that despite predomination of molecular-genetic methods of examinations nowadays, morphological and immunohistological evaluation of the damaged muscles did not lose its actuality. This is because it is not always possible to perform genetic analysis in the patient due to technical complexity of the procedure, use of costly equipment, many genetic mutations. Therefore, in some forms of muscular dystrophies (for example, in dysferlinopathies) of primary importance is morphological and immunohistological analysis of biopsy material. Nevertheless, this method should not be considered as most precise due to similarity of the morphology of different kinds of muscular dystrophies. Thus, correct diagnosis always requires systemic approach including comprehensive examination of the patient with use of maximally available methods. This is necessary for genetic consultations of patient, determination of peculiarities of therapy and for inclusion of patients in clinical trials.


2021 ◽  
pp. 1-10
Author(s):  
Fatih Hanci

Abstract Considering the high importance of leek as a vegetable crop, this species is rarely an object of molecular genetic studies. In this study, SRAP and ISSR markers were used for the first time to investigate the genetic diversity in Turkish leek accessions together with some morphological characters. The study was conducted in Erciyes University Faculty of Agriculture in 2018–2020. Thirty-seven local varieties were collected from different towns in Turkey. Also, nineteen leek accessions, which originated from different regions of Turkey, had been kindly obtained from Plant Gene Banks, USDA. Seventeen SRAP and three ISSR markers were screened; all of them exposing 137 reproducible bands, of which 114 resulted in polymorphic. Polymorphism information content (PIC) varied between 0.209 and 0.840. Genetic similarities varied from 0.563 to 0.960, with an average of 0.789. In addition to molecular markers, the entire gene pool was morphologically characterized over two-year data. For this purpose, eight characters, which play a key role in leek breeding, were measured. At the end of the study, the analyzes made according to the molecular and morphological data were compared both separately and in combination. In all groupings, it was found remarkable that the accessions numbered 98*3, 40*1, 40*4, and 40*6 were positioned differently from the others. These results have provided important insights into the genetic variability of Turkish leek accessions for the first time. Also, the diversity analysis performed in this study provides valuable information to researchers for future studies.


Genetika ◽  
2015 ◽  
Vol 47 (3) ◽  
pp. 1123-1130 ◽  
Author(s):  
Elizabeta Miskoska-Milevska ◽  
Zoran Popovski ◽  
Blagica Dimitrievska ◽  
Katerina Bandzo

Commonly used method for determination of the genetic diversity among the populations is the test for genetic differentiation. DNA microsatellite markers are usually used to investigate the genetic structure of natural populations. The aim of this study was to evaluate the applicability of eight DNA microsatellite loci (LECH13, LE21085, LEMDDNa, LEEF1Aa, LELEUZIP, LE20592, TMS9 and LE2A11) in genetic differentiation of six morphologically different tomato varieties (var. grandifolium from subsp. cultum; var. cerasiforme - red and yellow, var. pruniforme and var. pyriforme from subsp. subspontaneum; and var. racemigerum from subsp. spontaneum). The fragment analyses was performed using Applied Biosystems DNA analyzer (ABI 3130) and GeneMapper? Software program. The data were analysed using the specific program Power Marker Software. The average number of detected alleles was 3,625. Also, the average PIC value for all 8 DNA microsatellites loci was 0,3571. The genetic differentiation test in the researched tomato subspecies showed minor differentiation for locus LELEUZIP (- 0,0009), modest differentiation for locus LECH13 (0,0896), locus LEMDDNa (0,0896) and locus LE21085 (0,0551) and major differentiation for locus LE2A11 (0,7633), locus LEEF1Aa (0,6167), locus TMS9 (0.4967) and locus LE20592 (0,4263). On the other hand, in the estimated tomato varieties, locus LE21085 (0,0297), locus LECH13 (0,0256) and locus LELEUZIP (0,0005) showed minor differentiation, locus LEMDDNa (0,1333) showed modest differentiation, while locus TMS9 (0,5929), locus LEEF1Aa (0,5006), locus LE2A11 (0,4013) and locus LE20592 (0,2606) showed major differentiation. The eight DNA microsatellite loci can be applicable solution for tomato genetic differentiation. The overall results suggest that these microsatellite loci could be used in further population genetic studies of tomatoes.


2021 ◽  
pp. 147-154
Author(s):  
S. A. Kostiuk ◽  
O. S. Poluyan ◽  
M. V. Simirski ◽  
I. P. Marjenko

Objective: to identify the molecular genetic criteria of the risk of tension-type headache and migraine chronization development.Materials and methods. The detection of the results for the determination of allelic variants was carried out by means of horizontal electrophoresis using a molecular weight marker. The determination of the genotypes of the polymorphic variants of genes was carried out using high resolution melting PCR analysis.Results. Based on the performed molecular genetic studies, it has been established that the statistically significant (p < 0.05) risk factors of tension-type headache chronization are: the identification of the A-allele and AA-genotype of the DBH3 polymorphism of the dopamine-beta-hydroxylase gene DBH, as well as the identification of the G-allele and the GG-genotype of the Intron3SNP polymorphism of the preprotachykinin gene TAC1. It has been found that the statistically significant (p < 0.05) risk factors of migraine chronization are: the identification of the A-allele, GA- and AA-genotypes of the G29A polymorphism of the serotonin transporter gene SLC6A4, as well as the identification of the G-allele and the GG-genotype of the rs7793277 polymorphism of the preprotachykinin gene TAC1.Conclusion. The detection of these polymorphisms of the dopamine and preprotachykinin genes in the blood serum increases the risk of tension headache chronization by 1.395–1.991 times; the risk of migraine chronization by 1.235–1.395 times.


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