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1.
Journal of Southern Medical University ; (12): 567-571, 2011.
Article in Chinese | WPRIM | ID: wpr-307883

ABSTRACT

<p><b>OBJECTIVE</b>To identify the genetic susceptibility to Kashin-Beck disease (KBD) and explore the interaction between low selenium (Se) and the susceptibility gene loci in KBD.</p><p><b>METHODS</b>The DNA samples collected from 23 KBD nuclear families were analyzed using PCR and GeneScan Analysis 3.7 and Genotyper3.7 software. The haplotype relative risk (HRR) and transmission disequilibrium test (TDT) were used to test the data of the genotypes. The serum selenium (Se) concentration was measured by atomic fluorescence spectrometry, and the interaction between low Se and the susceptibility loci was calculated using a binary logistic regression.</p><p><b>RESULTS</b>In the 23 nuclear families, the alleles of D2S151 (248 bp), D2S305 (320 bp), and D11S4094 (194 bp) showed significant correlation to KBD (P<0.05). Serum Se concentrations in the studied individuals was 0.037 µg/ml. No significant statistical interaction was observed between low Se exposure and the susceptibility loci (P>0.05).</p><p><b>CONCLUSION</b>The polymorphisms in the STR loci D2S305, D2S151, and D11S4094 or the polymorphism loci near them might been related to KBD susceptibility. Low Se exposure shows no significant interaction with the susceptibility loci.</p>


Subject(s)
Adolescent , Adult , Child , Female , Humans , Male , Middle Aged , Young Adult , Alleles , Gene Frequency , Genetic Predisposition to Disease , Genotype , Kashin-Beck Disease , Blood , Genetics , Microsatellite Repeats , Pedigree , Selenium , Blood
2.
Chinese Journal of Biotechnology ; (12): 112-116, 2002.
Article in Chinese | WPRIM | ID: wpr-231385

ABSTRACT

5' and 3' flanking region of ovine BLG were amplified from sheep genomic DNA according to the published whole sequence of ovine BLG and cloned to pGEM-T vector correspondently. By partially sequencing, the sequences of BLG 5' and 3' flanking were the same as that of publication completely. The recombinant structure used to direct exogenous gene especially to express in mammary gland was constructed by joining 4.2 kb 5' flanking with 2.1 kb 3' flanking. In order to assess the efficiency of BLG regulatory elements, green fluorescent protein (GFP) gene as a reporter was fused with BLG construct and transfected the mammary epithelial cells (TD47). Through observation under UV microscope and detection by fluorometer, it is demonstrated that the GFP has been successfully expressed in TD47 cell line. By virtue of direct observation and quantitative analysis, the BLG-GFP construct can be served as a model for the quick assessment of mammary gland expression construct.


Subject(s)
Animals , 3' Flanking Region , Genetics , 5' Flanking Region , Genetics , Breast , Cell Biology , Cell Line , Cloning, Molecular , Gene Expression Regulation , Genes, Reporter , Green Fluorescent Proteins , Lactoglobulins , Genetics , Luminescent Proteins , Genetics , Sheep
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