2005•Zhonghua liuxingbingxue zazhiRequires access

Analysis on allele frequencies of 7 short tandem repeat loci of Kashing-Beck disease patients on chromosome 12

Lai Jiang-hua

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Abstract

Objective To analyze the allele frequencies of 7 short tandem repeat (STR) loci (D12S1718,D12S1675,D12S358,D12S367,D12S1638,D12S1646 and D12S1682) on chromosome 12 among Kashing-Beck disease(KBD) patients and the control population living in the KBD areas and non KBD area. Methods EDTA-blood specimens were collected from 102 unrelated individuals of Chinese Han population in Shaanxi province including 29 KBD patients,30 controls living in the KBD area and 43 living in the non-KBD area. DNA samples were extracted using the Wizard Genomic DNA purification kit (http://www. Promega. com) and were amplified by polymerase chain reaction (PCR) technique. The PCR products were analyzed by ABI 3100 Genetic Analyzer. Results (1) In KBD patients group, the allele number for 7 STR loci were 4,7,7,8,5,5 and 7,the genotype number were 5,12,13,11,10,9 and 13;(2) In the control population living in KBD area,the allele number for 7 STR loci were 4,9,7,6,6,6 and 8, the genotype number were 5,10,12,14,12,9 and 13; (3) In the control population living in the non-KBD area, the allele number for 7 STR loci were 7,9,7,7,5,8 and 11, the genotype number were 9,16, 17,16,12,15 and 20;(4) Compared with the allele frequencies among three groups,there were significant differences between KBD patients and the controls living in the KBD area (D12S367: P= 0.034; D12S1638: P=0.041) and the controls living in the non-KBD area(D12S367: P = 0. 029;D12S1638: P= 0.028) in the D12S367 and D12S1638 loci; (5) There were significant differences among KBD patients (P = 0. 036), controls living in the KBD area (P = 0.039) and controls living in the non-KBD area in the D12S1646. Conclusion There was significant difference between KBD patients and the controls in the D12S367 and D12S1638 loci.

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Objective To analyze the allele frequencies of 7 short tandem repeat (STR) loci (D12S1718,D12S1675,D12S358,D12S367,D12S1638,D12S1646 and D12S1682) on chromosome 12 among Kashing-Beck disease(KBD) patients and the control population living in the KBD areas and non KBD area. Methods EDTA-blood specimens were collected from 102 unrelated individuals of Chinese Han population in Shaanxi province including 29 KBD patients,30 controls living in the KBD area and 43 living in the non-KBD area. DNA samples were extracted using the Wizard Genomic DNA purification kit (http://www. Promega. com) and were amplified by polymerase chain reaction (PCR) technique. The PCR products were analyzed by ABI 3100 Genetic Analyzer. Results (1) In KBD patients group, the allele number for 7 STR loci were 4,7,7,8,5,5 and 7,the genotype number were 5,12,13,11,10,9 and 13;(2) In the control population living in KBD area,the allele number for 7 STR loci were 4,9,7,6,6,6 and 8, the genotype number were 5,10,12,14,12,9 and 13; (3) In the control population living in the non-KBD area, the allele number for 7 STR loci were 7,9,7,7,5,8 and 11, the genotype number were 9,16, 17,16,12,15 and 20;(4) Compared with the allele frequencies among three groups,there were significant differences between KBD patients and the controls living in the KBD area (D12S367: P= 0.034; D12S1638: P=0.041) and the controls living in the non-KBD area(D12S367: P = 0. 029;D12S1638: P= 0.028) in the D12S367 and D12S1638 loci; (5) There were significant differences among KBD patients (P = 0. 036), controls living in the KBD area (P = 0.039) and controls living in the non-KBD area in the D12S1646. Conclusion There was significant difference between KBD patients and the controls in the D12S367 and D12S1638 loci.

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Available abstract

Objective To analyze the allele frequencies of 7 short tandem repeat (STR) loci (D12S1718,D12S1675,D12S358,D12S367,D12S1638,D12S1646 and D12S1682) on chromosome 12 among Kashing-Beck disease(KBD) patients and the control population living in the KBD areas and non KBD area. Methods EDTA-blood specimens were collected from 102 unrelated individuals of Chinese Han population in Shaanxi province including 29 KBD patients,30 controls living in the KBD area and 43 living in the non-KBD area. DNA samples were extracted using the Wizard Genomic DNA purification kit (http://www. Promega. com) and were amplified by polymerase chain reaction (PCR) technique. The PCR products were analyzed by ABI 3100 Genetic Analyzer. Results (1) In KBD patients group, the allele number for 7 STR loci were 4,7,7,8,5,5 and 7,the genotype number were 5,12,13,11,10,9 and 13;(2) In the control population living in KBD area,the allele number for 7 STR loci were 4,9,7,6,6,6 and 8, the genotype number were 5,10,12,14,12,9 and 13; (3) In the control population living in the non-KBD area, the allele number for 7 STR loci were 7,9,7,7,5,8 and 11, the genotype number were 9,16, 17,16,12,15 and 20;(4) Compared with the allele frequencies among three groups,there were significant differences between KBD patients and the controls living in the KBD area (D12S367: P= 0.034; D12S1638: P=0.041) and the controls living in the non-KBD area(D12S367: P = 0. 029;D12S1638: P= 0.028) in the D12S367 and D12S1638 loci; (5) There were significant differences among KBD patients (P = 0. 036), controls living in the KBD area (P = 0.039) and controls living in the non-KBD area in the D12S1646. Conclusion There was significant difference between KBD patients and the controls in the D12S367 and D12S1638 loci.

Key concepts: Genotype, Allele, Genetics, Biology, Allele frequency, Population, Polymerase chain reaction, Medicine

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Analysis on allele frequencies of 7 short tandem repeat loci of Kashing-Beck disease patients on chromosome 12 — Research Paper | ScholarLens