Project/Area Number |
01570941
|
Research Category |
Grant-in-Aid for General Scientific Research (C)
|
Allocation Type | Single-year Grants |
Research Field |
Obstetrics and gynecology
|
Research Institution | Tokyo Women's Medical College |
Principal Investigator |
NAKABAYASHI Masao Tokyo Women's Medical College, Maternal and Perinatal Center, Professor, 医学部, 教授 (70114585)
|
Co-Investigator(Kenkyū-buntansha) |
AMAMIYA Teruko Department of Obstetrics and Gynecology, Assistant, 医学部, 助手 (00211011)
|
Project Period (FY) |
1989 – 1990
|
Project Status |
Completed (Fiscal Year 1990)
|
Budget Amount *help |
¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 1990: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1989: ¥1,000,000 (Direct Cost: ¥1,000,000)
|
Keywords | Thrombomodulin / DNA polymorphism / Protein C-activating cofactor activity / Polymerase chain reaction / PCR法 / 重症妊娠中毒症 / 糖尿病 / 遣伝子多型性 / recombinant TM / ドットハイブリダイゼ-ション / 血管病変 / 早期発症型重症妊娠中毒症 / プロテインC活性化能 / Lineweaber burk plot |
Research Abstract |
The existence of two types of thrombomodulin (TM) alleles has been reported by several researchers. One type of TM allele has Val residue on position #455 (Val455-TM), and the other has an Ala on the same position (Ala455-TM). On cloning TM genes fr13EA\ : om two severe preeclamptic patients, we have found both types of the alleles in one patient and the Ala455-TM allele in the other. Suspecting some relationship with these alleles and severe preeclampsia, we evaluated distributions of the two types o13EA\ : f alleles among 20 normal pregnant women, 9 with severe preeclampsia and 19 with diabetes mellitus (DM), using PCR-mediated amplification of genomic DNA and hybridization of allelespecific oligonucleotide probes to the amplified DNA.All possible ge13EA\ : notypes (Val/Val, Val/Ala, Ala/Ala) were found in each group. Each TM allele was produced recombinantly in Cos-I cells and both Val455-TM aeele and Ala455-TM allele were equally active in protein C activation. We concluded that these two types of TM13EA\ : alleles are functionally equivalent, normal genes.
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