In the present study with Tan sheep, small-tailed Han sheep, Hu sheep, Tong sheep, and Wadi sheep, we detected the distribution of gene frequency of several microsatellite sites in different chromosomes, the result sh...In the present study with Tan sheep, small-tailed Han sheep, Hu sheep, Tong sheep, and Wadi sheep, we detected the distribution of gene frequency of several microsatellite sites in different chromosomes, the result showed that： 1） Hu sheep was in the status of Hardy-Weinberg extreme disequilibrium （P 〈 0.01）, while populations including Tong sheep, small-tailed Han sheep, Tan sheep, and Wadi sheep were in Hardy-Weinberg equilibrium （P 〉 0.05）. 2） Variance analysis of the heterozygosity and poly- morphic information content at rnicrosatellite makers showed that there were not significant differences among populations as to heterozygosity and PIC （P 〉 0.05）, as to effective number of alleles there were not significant differences both among Tan sheep, Hu sheep, Tong sheep, and Wadi sheep, and between Wadi sheep and small-tailed sheep （P 〉 0.05）, but between the former three populations and the latter two populations, there were significant differences （0.01〈 P 〈0.05）. The variation levels of small-tailed Han sheep was the highest in the five populations based on microsatellite maker data, subsequently followed by Wadi sheep, Tong sheep, Tan sheep, and then Hu sheep. 3） The phylogenetic relationships of the five sheep populations in this study did not meet the mechanism of isolation by distance, and the genetic differentiation relationships among five sheep populations were not closely linearly correlative with their geography distribution. Our findings supported related records in literature： The five populations originated on different time stage from the primogenitor population and communicated genetically with each other thereafter in the process of natural and artificial selection and on different ecological environment.展开更多
In the present paper, RAPD was used to study the genetic polymorphism of fisheswith different genome combinations. Our results indicated that four of the 26 random primersproduced distinct and reproducible electrophor...In the present paper, RAPD was used to study the genetic polymorphism of fisheswith different genome combinations. Our results indicated that four of the 26 random primersproduced distinct and reproducible electrophoretic patterns which were genome-specific andcould distinguish different biotypes. This enabled us to derive a diagnostic profile, from whichwe constructed a molecular marker key for different biotypes. By the analysis of the data ofRAPD patterns, the genetic relationship was constructed with UPGMA (unweighted pair-groupmethod with arithmetical averages). Our experiments also concluded that RAPD was moresuccessful in variety identification than protein polymorphism analysis and serohematology for itstechnological simplicity and sensitivity.展开更多
Fifty two accessions of Festuca pratensis Huds. were analysed of which 18 had been collected in Switzerland and 32 in Bulgaria. SDS-PAGE of seed proteins was implemented to detect genetic variation among ecotype popul...Fifty two accessions of Festuca pratensis Huds. were analysed of which 18 had been collected in Switzerland and 32 in Bulgaria. SDS-PAGE of seed proteins was implemented to detect genetic variation among ecotype populations using a modification of UPOV method for barley. The modification concerns mainly protein extracting procedure as detailed described in the protocol. The two cultivars Preval and Cosmolit were used as standards. Cluster analyses and correspondence analyses/scatter plot were used as statistic approaches for determining genetic diversity among individual ecotypes and groups of ecotypes. Electrophoretic spectra of proteins show clear differences among local accessions in relation to their origin. In Swiss ecotypes 32 protein fragments were determined whereas in Bulgarian local populations their number was 68. Each of the two eco-groups possesses fragments that appear in all accessions of the group. The number of monomorphic bands within Bulgarian local ecotypes is four whereas their number in Swiss ecotypes is 12. Four monomorphic bands appearing in all proteinograms no difference of eco-groups was identified with Rm values of： 0.43, 0.55, 0.58, 0.82. A higher level of protein band polymorphism was proven in Bulgarian ecotypes in comparison with Swiss ecotypes. Thirty seven polymorphic bands occurred exclusively in the Bulgarian local ecotypes and had a frequency of 0.03 or higher whereas within Swiss ecotypes was detected one unique protein fragment. SDS-PAGE ＂fingerprinting＂ is suggested as a fast and easy approach to differentiate F. pratensis ecotypes by their origin as well for detection of foreign germplasm for inclusion in breeding programs.展开更多
Buffaloes （Bubalus bubalis） are widely distributed and were introduced to Brazil in 1895. Most of the molecular genetic characterization of buffaloes has been done with cross-specific （cattle） markers, but few of ...Buffaloes （Bubalus bubalis） are widely distributed and were introduced to Brazil in 1895. Most of the molecular genetic characterization of buffaloes has been done with cross-specific （cattle） markers, but few of them include Brazilian populations. Nineteen commonly used cattle microsatellites were tested to develop a multiplexed set of microsatellites and characterize Brazilian buffalo. Three PCR mixes were finally developed with the 11 markers that succeed in amplify and were polymorphic （58%）. The average number of alleles was 5.42, with an average observed and expected heterocigozity of 0.441 and 0.695, respectively. As it was expected, Brazilian buffalo variability was lower than the previously reported from the domestication centres （China and India）, but higher than the seriously selected European populations. The exclusion power calculated for the eleven markers in Brazilian buffalo was 0.9999999996, this allows its use in DNA based traceability.展开更多
基金This work was supported by the International Cooperation Item of the National Natural Science Foundation of China (No. 30213009, 30310103007, 30410103150)Natural Science Foundation of Jiangsu Province of China (No. BK2007556)+1 种基金Basic Natura Science Foundation for Colleges and Universities Jiangsu Province (No. NK051039, 06KJD230203)the New Century Talent Project of Yangzhou University in China.
文摘In the present study with Tan sheep, small-tailed Han sheep, Hu sheep, Tong sheep, and Wadi sheep, we detected the distribution of gene frequency of several microsatellite sites in different chromosomes, the result showed that： 1） Hu sheep was in the status of Hardy-Weinberg extreme disequilibrium （P 〈 0.01）, while populations including Tong sheep, small-tailed Han sheep, Tan sheep, and Wadi sheep were in Hardy-Weinberg equilibrium （P 〉 0.05）. 2） Variance analysis of the heterozygosity and poly- morphic information content at rnicrosatellite makers showed that there were not significant differences among populations as to heterozygosity and PIC （P 〉 0.05）, as to effective number of alleles there were not significant differences both among Tan sheep, Hu sheep, Tong sheep, and Wadi sheep, and between Wadi sheep and small-tailed sheep （P 〉 0.05）, but between the former three populations and the latter two populations, there were significant differences （0.01〈 P 〈0.05）. The variation levels of small-tailed Han sheep was the highest in the five populations based on microsatellite maker data, subsequently followed by Wadi sheep, Tong sheep, Tan sheep, and then Hu sheep. 3） The phylogenetic relationships of the five sheep populations in this study did not meet the mechanism of isolation by distance, and the genetic differentiation relationships among five sheep populations were not closely linearly correlative with their geography distribution. Our findings supported related records in literature： The five populations originated on different time stage from the primogenitor population and communicated genetically with each other thereafter in the process of natural and artificial selection and on different ecological environment.
文摘In the present paper, RAPD was used to study the genetic polymorphism of fisheswith different genome combinations. Our results indicated that four of the 26 random primersproduced distinct and reproducible electrophoretic patterns which were genome-specific andcould distinguish different biotypes. This enabled us to derive a diagnostic profile, from whichwe constructed a molecular marker key for different biotypes. By the analysis of the data ofRAPD patterns, the genetic relationship was constructed with UPGMA (unweighted pair-groupmethod with arithmetical averages). Our experiments also concluded that RAPD was moresuccessful in variety identification than protein polymorphism analysis and serohematology for itstechnological simplicity and sensitivity.
文摘Fifty two accessions of Festuca pratensis Huds. were analysed of which 18 had been collected in Switzerland and 32 in Bulgaria. SDS-PAGE of seed proteins was implemented to detect genetic variation among ecotype populations using a modification of UPOV method for barley. The modification concerns mainly protein extracting procedure as detailed described in the protocol. The two cultivars Preval and Cosmolit were used as standards. Cluster analyses and correspondence analyses/scatter plot were used as statistic approaches for determining genetic diversity among individual ecotypes and groups of ecotypes. Electrophoretic spectra of proteins show clear differences among local accessions in relation to their origin. In Swiss ecotypes 32 protein fragments were determined whereas in Bulgarian local populations their number was 68. Each of the two eco-groups possesses fragments that appear in all accessions of the group. The number of monomorphic bands within Bulgarian local ecotypes is four whereas their number in Swiss ecotypes is 12. Four monomorphic bands appearing in all proteinograms no difference of eco-groups was identified with Rm values of： 0.43, 0.55, 0.58, 0.82. A higher level of protein band polymorphism was proven in Bulgarian ecotypes in comparison with Swiss ecotypes. Thirty seven polymorphic bands occurred exclusively in the Bulgarian local ecotypes and had a frequency of 0.03 or higher whereas within Swiss ecotypes was detected one unique protein fragment. SDS-PAGE ＂fingerprinting＂ is suggested as a fast and easy approach to differentiate F. pratensis ecotypes by their origin as well for detection of foreign germplasm for inclusion in breeding programs.
文摘Buffaloes （Bubalus bubalis） are widely distributed and were introduced to Brazil in 1895. Most of the molecular genetic characterization of buffaloes has been done with cross-specific （cattle） markers, but few of them include Brazilian populations. Nineteen commonly used cattle microsatellites were tested to develop a multiplexed set of microsatellites and characterize Brazilian buffalo. Three PCR mixes were finally developed with the 11 markers that succeed in amplify and were polymorphic （58%）. The average number of alleles was 5.42, with an average observed and expected heterocigozity of 0.441 and 0.695, respectively. As it was expected, Brazilian buffalo variability was lower than the previously reported from the domestication centres （China and India）, but higher than the seriously selected European populations. The exclusion power calculated for the eleven markers in Brazilian buffalo was 0.9999999996, this allows its use in DNA based traceability.
