TY - JOUR
T1 - Determination of microsatellite repeats in the human thyroid peroxidase (TPOX) gene using an automated gene analysis system with nanoscale engineered biomagnetite
AU - Nakagawa, Takahito
AU - Maruyama, Kohei
AU - Takeyama, Haruko
AU - Matsunaga, Tadashi
N1 - Funding Information:
This work was funded in part by a Grant-in-Aid for Specially Promoted Research, No. 13002005 from the Scientific Research for the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2007/4/15
Y1 - 2007/4/15
N2 - The number of repeat in the microsatellite region (AATG)5-14 of the human thyroid peroxidase gene (TOPX) was determined using an automated DNA analysis system with nano-scale engineered biomagnetite. Thermal melting curve analysis of DNA duplexes on biomagnetite indicated that shorter repeat sequences (less than 9 repeats) were easily discriminated. However, it was difficult to determine the number of repeats at more than nine. In order to improve the selectivity of this method for the longer repeats, a "double probe hybridization assay" was performed in which an intermediate probe was used to replace a target repeat sequence having more than 9 repeats with a shorter sequence possessing less than 9 repeats. Thermal probe melting curve analyses and Tm determination confirmed that the target with 10 repeats was converted to 5 repeats, 11 repeats converted to 4 and 12 to 3, respectively. Furthermore, rapid determination of repeat numbers was possible by measuring fluorescence intensities obtained by probe dissociation at 56 and 66 °C, and 40, 60 and 80 °C for signal normalization.
AB - The number of repeat in the microsatellite region (AATG)5-14 of the human thyroid peroxidase gene (TOPX) was determined using an automated DNA analysis system with nano-scale engineered biomagnetite. Thermal melting curve analysis of DNA duplexes on biomagnetite indicated that shorter repeat sequences (less than 9 repeats) were easily discriminated. However, it was difficult to determine the number of repeats at more than nine. In order to improve the selectivity of this method for the longer repeats, a "double probe hybridization assay" was performed in which an intermediate probe was used to replace a target repeat sequence having more than 9 repeats with a shorter sequence possessing less than 9 repeats. Thermal probe melting curve analyses and Tm determination confirmed that the target with 10 repeats was converted to 5 repeats, 11 repeats converted to 4 and 12 to 3, respectively. Furthermore, rapid determination of repeat numbers was possible by measuring fluorescence intensities obtained by probe dissociation at 56 and 66 °C, and 40, 60 and 80 °C for signal normalization.
KW - Automated system
KW - Bacterial magnetic particles (BacMps)
KW - DNA hybridization
KW - Melting temperature
KW - Microsatellite
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U2 - 10.1016/j.bios.2006.11.025
DO - 10.1016/j.bios.2006.11.025
M3 - Article
C2 - 17204413
AN - SCOPUS:33847379717
SN - 0956-5663
VL - 22
SP - 2276
EP - 2281
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
IS - 9-10
ER -