| Project/Area Number |
08044320
|
|---|
| Research Category |
Grant-in-Aid for international Scientific Research
|
| Allocation Type | Single-year Grants |
|---|
| Section | Joint Research |
|---|
| Research Field |
Pediatrics
|
|---|
| Research Institution | Keio University |
|---|
Principal Investigator |
SHIMIZU Nobuyoshi Keio University, School of Medicine, Department of Molecular Biology, Professor, 医学部, 教授 (50162706)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
ANTONARAKIS スティタアノス ジュネーブ大, 医学部, 教授
ASAKAWA Shuichi Keio University School of Medicine, Department of Molecular Biology, Assistant, 医学部, 助手 (30231872)
KAWASAKI Kazuhiko Keio University School of Medicine, Department of Molecular Biology, Assistant, 医学部, 助手 (90245465)
KUDOH Jun Kieo University School of Medicine, Department of Molecular Biology, Assistant, 医学部, 助手 (80178003)
MINOSHIMA Shinsei Keio University School of Medicine, Department of Molecular Biology, Assistant P, 医学部, 講師 (90181966)
ANTONARAKIS Stylianos Univ.of Geneva Medical School, Division of Medical Genetics, Professor
ANTONARAKIS エス ジュネーブ大学, 医学部, 教授
MCDERMID He アルバータ大, 医学部, 教授
KOLA Ismail モナシュ大, 生殖発生研, 教授
ANTONARAKIS スティリアノス ジュネーブ大, 医学部, 教授
EMANUEL Bev ペンシルベニア大学, 医学部, 教授
|
|---|
| Project Period (FY) |
1996 – 1997
|
| Project Status |
Completed (Fiscal Year 1997)
|
| Budget Amount *help |
¥8,000,000 (Direct Cost: ¥8,000,000)
Fiscal Year 1997: ¥4,200,000 (Direct Cost: ¥4,200,000)
Fiscal Year 1996: ¥3,800,000 (Direct Cost: ¥3,800,000)
|
|---|
| Keywords | cardiac defects / exon trapping / genome sequencing / cDNA screening / transcription factor / morphogenesis / autoimmune disease / immune tolerance / ダウン症候群 / コスミドクローン / SIM2遺伝子 / トランスジェニックマウス / BACクローン / 猫目症候群 |
|---|
| Research Abstract |
To isolate novel genes involved in the morphogenesis of heart, we performed exon trapping and genomic sequencing of the DNA contigs of human chromosomes 21 and 22. We also employed cDNA screening of heart cDNA library. We have isolated several novel genes from chromosome 21 including SIM (single-minded), MNB (minibrain), KNP (keio novel protein)1, KNP3, KNP4 and so on. In collaboration with Professor Antonarakis, we found two SIM genes, SIM1 and SIM2, and determined their genomic structures and tissue expresseion patterns. The SIM genes are thought to be functioning as trascription factors during the brain development. We found a cDNA clone which is expressed only in the heart of embryos but its entire structure is not yet unveiled. In collaboration with Professor McDermid, we detected a new gene which is a human homolog of mouse Bid2 gene which is believed to regulate certain cell types during the morphogenesis of heart. Thus, we have made a good progress for the past two years. Moreover, we were able to isolate another new gene AIRE which is responsible for the pathogenesis of an autoimmune disease APECED.The AIRE gene produces a pathogenesis of an autoimmune disease APECED.The AIRE gene produces a transcription factor which seems to play a role in regulating the maturation process of immune response. this finding was made in collaboration with Professors Antonarakis and Krohn. We had a mini-symposium on the autoimune disease by inviting these two professors and their research fellows to exchange ideas together with 70 audiences. During their stay, we had fruitful discussion and determined future directions of our collaboration.
|
