| Project/Area Number |
10557099
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 展開研究 |
|---|
| Research Field |
Endocrinology
|
|---|
| Research Institution | Fukui Medical University (1999)
Gunma University (1998) |
|---|
Principal Investigator |
MIYAMOTO Kaoru Fukui Medical University, Department of Biochemistry, Professor, 医学部, 教授 (30125877)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
INAZU Tetsuya Fukui Medical University, Department of Biochemistry, Assistant Professor, 医学部, 助手 (00242587)
YAMADA Kazuya Fukui Medical University, Department of Biochemistry, Associate Professor, 医学部, 助教授 (20263238)
峯岸 敬 群馬大学, 医学部, 講師 (00209842)
保坂 公平 群馬大学, 医学部, 教授 (70108992)
|
|---|
| Project Period (FY) |
1998 – 1999
|
| Project Status |
Completed (Fiscal Year 1999)
|
| Budget Amount *help |
¥6,500,000 (Direct Cost: ¥6,500,000)
Fiscal Year 1999: ¥2,400,000 (Direct Cost: ¥2,400,000)
Fiscal Year 1998: ¥4,100,000 (Direct Cost: ¥4,100,000)
|
|---|
| Keywords | ovary / human homologue / inducible gene / transcription factor / 転写因子 / 腫瘍 / 遺伝子診断 |
|---|
| Research Abstract |
In order to develop a gene diagnostic system for ovarian dysfunction using a novel ovarian transcription factor GIOT, we have cloned human homologues of GIOT and investigated the possible roles of GIOT for the ovarian functions. An expression plasmid containing GIOT was constructed and rat granulosa cells were transfected with the plasmid. Reporter plasmids containing ovarian genes were simultaneously transfected and the reporter activity was measured. The transfection study demonstrated that GIOT can suppress the ovarian gene expression and works as an ovarian transcription repressor. MA10 mouse Leydig tumor cells were also transfected with the GIOT expression plasmid and similar results were obtained. Therefore, we demonstrated that GIOT actually works on the transcriptional regulation of ovarian genes. We also have cloned human homologues of GIOT. At least three human GIOT homologues were isolated. Nucleotide sequence analysis of these clones revealed that these are distinct genes. Functional analysis of these genes is now underway.
|
