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  • DNA  (8)
  • 2020-2022  (8)
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  • 1
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    In:  http://aquaticcommons.org/id/eprint/23658 | 18721 | 2018-07-15 07:37:24 | 23658 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-14
    Description: Molecular comparison of two parasites Lernaea cyprinacea and Lernaea ctenopharyngodoni was carried out using RAPD (Random Amplified Polymorphic DNA) technique. A total of 43 Lernaea specimens belonging to the two species were collected from the Guilan and Khouzestan Provinces. DNA was extracted using the Phenol-chloroform method. The quality and quantity of DNA was assessed using 1% Agarose gel electrophoresis and spectrophotometer. Polymerase Chain Reaction (PCR) was conducted on the target DNA under specific conditions and PCR products were subjected to electrophoresis on polyacrylamide gels (6%). Polyacrylamide gels were stained using silver nitrate and DNA bands were analyzed with BioCapt software. The genetic analysis was conducted using POP GEN 32 software. Forty two primers, 10 nucleotides each were used for PCR reaction. Totally, 397 RAPD loci were counted on polyacrylamide gel where 349 identical loci were polymorphic of which some bands may be used as genetic markers for the identification of both Lernaea species. Data analysis on PCR products showed higher genetic variation (1.15%) of L. ctenopharyngodon in the Guilan Province as compared to that of the Khouzestan (0.0%). However, genetic variation (27.46%) of L. cyprinacea in the Khouzestan Province was 7.26 times higher than that of the Guilan province (3.78%). The two species showed a genetic differentiation of approximately 88%. Based on the observed molecular differences, we state that L. ctenopharyngodoni is a genetically independent species from L. cyprinacea.
    Keywords: Biology ; Molecular structure ; Genetics ; DNA ; Freshwater ; Parasites ; Polymerase chain reaction ; Primers ; Nucleotides ; Lernaea ctenopharyngodoni ; Lernaea cyprinacea ; Gilan Province ; Khouzestan Province ; Iran
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 19-28
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  • 2
    Publication Date: 2021-07-15
    Description: A total of 28 specimens of adult Russian sturgeon brood fish from the Volga River (Astrakhan, Russia) and 42 specimens from the south Caspian Sea (coastline of Iran and Turkmenistan) were collected. About 2g of fin tissue was stored in 96% ethyl alcohol and transferred to the genetic laboratory of the International Sturgeon Research Institute. Genomic DNA was extracted using phenol-chloroform method. The quality and quantity of DNA was assessed by Agarose gel electrophoresis and spectrophotometry. Polymerase Chain Reaction (PCR) was conducted using eight pairs of microsatellite primers and its products were electrophoresed using 6% polyacrylamide gel followed by silver nitrate staining. Allele sizes were measured in all populations, then genetic parameters were calculated using Gen Alex program and the phylogenetic relationship was determined and drawn using TFPGA program. A minimum of 10 and a maximum of 21 alleles were identified per locus and the observed heterozygosity ranged between 0.50-0.96 and the expected heterozygosity was 0.74-0.90 with an average of 0.68. Hardy-Weinberg equilibrium was observed at Ls-19, Ls-39 loci, but showed disequilibrium in other loci. FST index between Volga and South Caspian Sea samples was 0.031. The genetic similarity and distance was 0.661 and 0.414, respectively. Results of the present investigation indicate that there are no significant differences between the south Caspian Sea Russian sturgeon specimens.
    Keywords: Biology ; Population Genetics ; Genes ; Electrophoresis ; Fins ; DNA ; Genetic diversity ; Natural populations ; Phylogenetics ; Phylogeny ; Heterozygosity ; Migration ; Alcohols ; Spectrophotometry ; Genomics ; Silver nitrate ; Genetic structure ; Rivers ; Microsatellites ; Gel electrophoresis ; Polymerase chain reaction ; Primers ; Coasts ; Acipenser gueldenstaedtii ; Acipenser ; Brackish ; Caspian Sea ; Caspian Sea Turkmenistan ; Iran
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 69-80
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  • 3
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    Iranian Fisheries Science Research Institute | Tehran, Iran
    In:  http://aquaticcommons.org/id/eprint/25519 | 18721 | 2018-10-05 15:40:50 | 25519 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-16
    Description: The Persian sturgeon (Acipenser persicus) is more abundant sturgeon species in the South Caspian Sea and consist the highest proportion of Iranian Caviar, meat as well as bringing maximum foreign currency income, however from systematic point of view and differentiation of this species from Russian sturgeon (Acipenser gueldenstadttii) a serious challenging issues remain, where some Russian scientist are believe that the Persian sturgeon is not as an valid species and consider it as a subspecies of Russian sturgeon. This research conducted with the objective of identification and introducing a molecular marker based on specific DNA for differentiation of two species of Persian sturgeon and Russian sturgeon via a proved molecular marker method. For this purposes 8 different molecular approaches such: Microsatellite, AFLP, RAPD, sequencing of Cytb, 16sDNA, ND5, Growth Hormone gene and finally Single Nucleotide Polymorphism (SNP) were investigated. Based on applied methodology, between 5 to 16 caudal fin tissues were sampled for each species from different region of the Caspian Sea, Sefiedrud River, Ural and Volga rivers. Following DNA extraction, its quality and quantity were determined and the PCR experiment has been conducted using 5-110 primers according to various methods and type of gene. The PCR products were electrophoresed on Polyacrilamid or agarose gels and followed by silver and Ethidium Bromide staining. In RAPD method, polymorphic DNA band was cut on the gel followed by purification and then the segments were cloned in vector in Top10 strain of E.coli, and then sequenced. Meanwhile for Growth Hormone gene in Persian and Russian sturgeon the MEGA 4, Gene runner software were used to design the appropriate primers for PCR amplification. The PCR products were cloned in PTZ57R/T vector and transformed in Top10 E.coli strain and sequenced finally. For all other genes, similar methods were applied for PCR amplification and its products were sequenced and statistical analysis as well as phylogenetical tree was performed. In Single Nucleotide Polymorphism (SNP) method, after genomic library construction, in total 14.4 billion nucleotides were sequenced and similarity/ differentiation analysis of two species were investigated using specific bioinformatic software. Results indicated that Microsatellite and AFLP methods showed high level of genetic variation both within and between species. The Cytb gene, when 4 sample sequences from each species were compared two species were differentiated, however when analysis repeated over 15 samples, the sequence comparison couldn't differentiate two above mentioned species. Full sequence comparison of 16sDNA and mtDNA-ND5 gene showed variation in some nucleotide in both species of Persian and Russian sturgeon but no significant. Results of sequences obtained from cloned segment with RAPD method and also specific primer design based on produced sequences could succeed to discover a variable DNA band that able to differentiate two species from each other. Results of the present study also showed that the growth hormone gene (GH) of Persian and Russian sturgeon consists of 645 nucleotide that translate to 214 Amino Acids. The sequence comparison indicated that the gene coding growth hormone in Persian and Russian sturgeon had the highest similarity with GH of Mammals (71%), Anguilaformes (63%) and less similarity with bony fish (37%). Phylogenetic analysis indicates that Persian and Russian sturgeon in compare to other organism are ancient species and this gene is originated from a common ancestor. At present study the most appropriate results obtained from Single Nucleotide Polymorphism (SNP) method by sequencing 14.4 billion nucleotide from genome of two species of Persian and Russian sturgeon from North and the South Caspian Sea could prove that the Persian sturgeon is a valid and independent specie. This excellent results is the biggest scientific achievement for differentiation of two highly commercial important sturgeon species in the Caspian Sea in last two decades.
    Keywords: Biology ; Iran ; Caspian Sea ; 16S rDNA ; Acipenser persicus ; Persian sturgeon ; Acipenser gueldenstadttii ; DNA ; Russian sturgeon ; Species differentiation ; Molecular Marker ; SNP
    Repository Name: AquaDocs
    Type: monograph
    Format: application/pdf
    Format: application/pdf
    Format: 239
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  • 4
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    In:  http://aquaticcommons.org/id/eprint/21699 | 18721 | 2017-11-27 12:11:39 | 21699 | University of Guilan, Faculty of Natural Resources, Iran
    Publication Date: 2021-06-28
    Description: In order to identify the sex marker in Mahisefied, Rutilus frisii kutum, samples from 5 male and 5 female fish were collected from the south Caspian Sea. Polymerase chain reaction random amplified polymorphic DNA (PCR-RAPD) was performed using 124 primer sets. All bands were numbered using 1 and 0 scores corresponding to the presence or absence of bands, respectively and data were analyzed using RAPDPLOT program. Results indicated that 44 sets of primers did not show any flanking site and produced no bands, while the remaining 80 produced sharp and visible bands on polyacrylamid gel. In total, 1600 bands were scored. However, none of the bands corresponded to either the male or female fish.According to the results it has been concluded that RAPD technique failed to detect sex and cannot be considered as a robust molecular tool for sex differentiation in the studied fish. The reason may be the absence of sex chromosomes in this species or that the genes corresponding to sex differentiation are spread on different autosomal chromosomes with interaction of some environmental factors.
    Keywords: Biology ; Fisheries ; failure ; PCR-RAPD ; technique ; differentiate ; sex ; mahisefied ; Rutilus frisii kutum ; Caspian Sea ; iran ; DNA
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 235-242
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  • 5
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    In:  http://aquaticcommons.org/id/eprint/21740 | 18721 | 2017-11-28 09:11:49 | 21740 | University of Guilan, Faculty of Natural Resources, Iran
    Publication Date: 2021-06-30
    Description: In sturgeon aquaculture, where the main purpose is caviar production, a reliable method is needed to separate fish according to gender. Currently, due to the lack of external sexual dimorphism, the fish are sexed by an invasive surgical examination of the gonads. Development of a non-invasive procedure for sexing fish based on genetic markers is of special interest. In the present study we employed Bulked Segregant Analysis (BSA) methodology to search for DNA markers associated with the sex of the beluga sturgeon (Huso huso). DNA bulks (male and female) were created by combining equal amounts of genomic DNA from 10 fish of both sexes. A total of 101 decamer primers associated with the sex-specific sequences in non-sturgeon species was used for targeted screening of the bulks, resulting in 2846 bands that all of them were present in both sexes. Our results showed that sex chromosomes are weakly differentiated in the sturgeon genome and comprised sequences not complementary to the sex-specific primers in non-sturgeon species.
    Keywords: Biology ; Fisheries ; genome ; beluga ; huso huso ; sex ; markers ; segregant ; DNA ; species ; Iran
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 185-195
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  • 6
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    In:  http://aquaticcommons.org/id/eprint/23674 | 18721 | 2018-07-17 03:28:56 | 23674 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-15
    Description: In order to introduce genetic markers of four species of fishes, 80 samples of each species, i.e. Parastromateus niger, Scomberomorus comersoniannus, Trachionotus mookalee and Caranx para were collected. DNA was extracted using phenol- chloroform method. The target gene (cytochrome b) was amplified by Thermal cycle (PCR) and the PCR product size estimated 1105 bp. In this research out of 27 DNAase enzymes which were used for PCR product enzyme digesting 8 enzymes (Bam HI, Alw 261, Rsa I, Mbo I, Alu I, Hinf I, Dpn I, Dde I) have cut side on target DNA and three enzymes of them Alu I, Hinf I and Mbo I showed polymorphism genetic differences while other enzymes displayed similar patterns. Variation of haplotypes from four species are as follows: BAA for P. niger, AAB for T. mookalee, ABA for C. para, and ACA for S. comersonianus. So it is possible to claim that each of the above Haplotypes may be used as genetic markers for each of the species.
    Keywords: Biology ; Genetics ; DNA ; Enzymes ; Biomarkers ; Identification ; Phenotypes ; Chloroform ; Haplotypes ; Gene polymorphism ; Genetic markers ; Caranx ; Marine ; Separation ; Polymerase chain reaction ; Phenotypic variations ; Cytochrome b ; DDE ; Trachionotus mookalee ; Parastromateus niger ; Caranx para ; Carangidae ; Scomberomorus comersoniannus ; Scomberomorus ; ISW ; Arabian Sea ; Oman Gulf ISW ; Persian Gulf ; Iran
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 1-14
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  • 7
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    In:  http://aquaticcommons.org/id/eprint/23700 | 18721 | 2018-07-18 08:50:22 | 23700 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-15
    Description: Population structure of Ship sturgeon, Acipenser nudiventris, from the south coast of Caspian Sea and Ural River was investigated using Microsatellite method. For this reason, 73 specimens of the sturgeon were collected from five locations in two sampling regions the first consisted of Bandar Anzali, SefidRud River, Babolsar, and Gorgan, and the second was Ural River. Four SSR markers were used in this investigation, of which 5 loci produced DNA band, with three of them being polymorph. One primer showed two loci with one of them being polymorph and another was monomorphic). Average expected and observed heterozygosity was 0.86 and 0.75 respectively. Genetic variation was assessed through analysis of molecular variance (AMOVA) that indicated almost all of the variance in data namely %94 (P less than or equal to 0.03) was within locations.
    Keywords: Biology ; Population Genetics ; DNA ; Genetic diversity ; Population structure ; Genotypes ; Biopolymorphism ; Aquaculture techniques ; Fish ; Sturgeon ; Populations ; Sexual Reproduction ; Rivers ; Anadromous species ; Nucleotide sequence ; Induced breeding ; Primers ; Ships ; Sampling ; Coasts ; Acipenser ; Acipenser nudiventris ; Brackish ; Caspian Sea ; Ural R. Eurasia ; Caspian Sea Eurasia ; Iran
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 99-108
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  • 8
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    In:  http://aquaticcommons.org/id/eprint/21736 | 18721 | 2017-11-28 09:02:29 | 21736 | University of Guilan, Faculty of Natural Resources, Iran
    Publication Date: 2021-06-30
    Description: This study was conducted in order to investigate genetic diversity and population structure of pike perch in the Northern part of Iran. For this purpose, 207 adult pike-perches from four regions of the Caspian Sea watershed (Talesh Coasts, Anzali Wetland, Chaboksar Coasts and Aras Dam) were collected. DNA was extracted and by using 15 pairs of microsatellite primers, Polymerase Chain Reaction (PCR) was conducted. DNA bands were analyzed using Biocapt and GenAlex 6 software package. Out of 15 microsatellite primers, 11 loci were produced, of those, 6 loci were polymorphic and 5 were monomorphic. Analysis revealed that the average number of alleles per locus and observed heterozygosities were not statistically significant (P〉0.05) for all four populations. Data indicated an appreciable genetic differentiation, in spite of a low genetic variation, and agreed with the low level of genetic polymorphism already observed for this species in Iran. Deviation from Hardy-Weinberg equilibrium was obvious in most cases, mostly due to the deficiency of heterozygosities. The highest genetic distance was between Anzali Wetland and Aras Dam populations. This investigation represents the first approach to the knowledge of the genetic variability of Iranian populations using microsatellite markers, and reported results could be of interest for future management and conservation programs of this species in Iran.
    Keywords: Biology ; Fisheries ; genetic ; Sander lucioperca ; populations ; microsatellite ; DNA ; markers ; iran ; polymorphism
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 99-108
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