| Project/Area Number |
11670428
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Legal medicine
|
|---|
| Research Institution | Kansai Medical University |
|---|
Principal Investigator |
AKANE Atsushi Kansai Medical University Faculty of Medicine Professor, 医学部, 教授 (70202520)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
OKII Yutaka Kansai Medical University Faculty of Medicine Instructor, 医学部, 助手 (20121915)
YOSHIDA Manabu Kansai Medical University Faculty of Medicine Assistant Professor, 医学部, 講師 (20122004)
WATABIKI Toshimitsu Kansai Medical University Faculty of Medicine Assistant Professor, 医学部, 講師 (70077692)
YOSHIMURA Sumitaka Kansai Medical University Faculty of Medicine Instructor, 医学部, 助手 (70167005)
|
|---|
| Project Period (FY) |
1999 – 2002
|
| Project Status |
Completed (Fiscal Year 2002)
|
| Budget Amount *help |
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2002: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2001: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2000: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1999: ¥1,400,000 (Direct Cost: ¥1,400,000)
|
|---|
| Keywords | inverse-PCR / intramolecular ligation / ABO blood group / MN blood group / Se blood group / Haplotype / personal identification / molecular evolution / 多型 / MNSs式血液型 / グリコフォリンA / PCR |
|---|
| Research Abstract |
We found that M allele of MN blood group system can be divided into two alleles M^G and M^T, and explored an allele-specific inverse-PCR amplification (ASIP) method to detect two polymorphic regions in the gene simultaneously. After the sequencing of glycophorin A gene, we found that the three alleles can be classified into more than 6 alleles, and discussed molecular evolution of the alleles. A new ASIP method was also investigated to detect these alleles.
Major alleles, A^1, B and O^1 are based on the base changes at exsons 6 and 7 of ABO gene, so that the ABO genotype should had been determined by detecting both regions individually. In this study, the separated polymorphic regions could be detected simultaneously by ASIP, restriction fragment length polymorphism and sequencing methods with inverse-PCR technique. Moreover, these methods were applied to detect a variant allele A^2, but were little informative to type genotype A_2B because no O allele was included.
Major alleles of Se blood group in Japanese are Se1, sej and se^<fus>. The se^<fus> allele was reported to be a fusion gene of Sec1 pseudogene and Se1 gene. However, we revealed several new findings on the fusion mechanism by sequencing the fusion gene. Based on the findings, we also explored the allele-specific PCR amplification and ASIP methods to genotype Se blood group. Then we found that flattening of the fragment ends by mung bean nuclease was quite effective for intramolecular ligation of the fragments prior to the inverse-PCR. By this procedure, the precision and applicability of the inverse-PCR-based genotyping methods could be increased.
|
