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The article presents a study in which researchers isolated and characterized polymorphic microsatellite loci derived from a microsatellite-enriched genomic library. A total of 296 recombinant clones were sequenced wherein 125 sequences were usable for primer design. Fifty-four loci showed polymorphism in the 24 individuals. The high levels of polymorphism and heterozygosity displayed at the loci indicate that these loci should provide a valuable tool for kinship and population studies.

Aim: A cross-section study was conducted to explore the association between polymorphism of δ-aminolevulinic acid dehydratase (ALAD) and lead poisoning in Uygur and Han children in China. Methods: The ALAD genotyping was determined by PCR-RFLP in 443 Uygur and 469 Han children aged 6–10 years from Urumqi in Xinjiang province. Results: The blood lead levels of 912 environmentally exposed children ranged from 0.5 to 48.2 μg/dL, with a mean of 5.45 μg/dL and a standard deviation of 0.22 μg/dL, and 23. Thirty-one percent individuals were with blood lead level ≥10 μg/dL. The mean and standard deviation of blood lead levels were 5.57 ± 0.223 μg/dL and 5.30 ± 0.224 μg/dL in Uygur and Han children, respectively. The frequencies of the allele ALAD1 and ALAD2 in Uygur subjects were 90.52% and 9.48%, and in Han subjects were 95.73% and 4.27%, respectively (chi-square = 19.55, p < 0.05). No statistic correlation between the distribution of ALAD alleles and the blood lead level was found in both populations. Conclusion: A significant difference was seen in the frequency distribution of ALAD genotype between the different races. The genetic susceptibility of ALAD polymorphism to lead toxicity may exhibit in a lead dose-dependent manner. [ABSTRACT FROM AUTHOR]

Focuses on the establishment of rDNA intergenic spacer structure of Cannabis sativa. Amplification of DNA fragments rDNA intergenic spacer; Comparison of the DNA sequence with all the plant sequences registered in GenBank by the Fasta program of GCG software; Importance of DNA polymorphism analysis.

The expression of autoimmunity in mice deficient in programmed death 1 (PD-1) suggests that PD-1 is a candidate gene involved in the development of human autoimmune diseases such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA). We therefore tested the potential association between PD-1 and the development of SLE and RA by conducting case–control genetic-association studies. Ninety-eight SLE patients, 84 RA patients, and sex-matched control subjects for each disease group were recruited and genotyped for a single-nucleotide polymorphism, C+872T, in the human PD-1 gene. The significance of the association of the PD-1 gene with SLE or with RA was analyzed by statistical tests for the difference in genotype distribution between disease and control groups. The human PD-1 gene was found to be significantly associated with disease development in RA patients, but not SLE patients. The risk of RA development appeared to be significantly increased by carriage of the T allele (odds ratio 3.32, P < 0.0001) or the C/T genotype (odds ratio 3.52, P < 0.00005). The PD-1 gene is significantly associated with RA susceptibility, suggesting the possibility that PD-1 may contribute to the pathogenesis of RA. [ABSTRACT FROM AUTHOR]