Research on the structure and functions of human FTZ-F1β gene
Research on the structure and functions of human FTZ-F1β gene
批准号:
10671039
负责人:
YANASE Toshihiko
金额:
$2.5万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 2000
中文摘要
FTZ-F1β被认为是Ad4BP的对应物,主要在肝脏和胰腺中表达。我们确定了人FTZ-F1β基因的结构。我们确定了外显子序列,包括外显子/内含子边界和5'侧区域的序列。该基因至少50 Kb长,分为8个外显子,包括一个非编码外显子1。人类FTZ-F1β基因的整体结构组织与人类Ad4BP/SF-1基因非常相似,表明两者均来源于共同祖先基因。此外,通过对人FTZ-F1β基因5'侧区域的一系列缺失分析,对人FTZ-F1β基因在Hep G2细胞中的转录调控进行了初步研究,发现转录位点上游-1743至-1040 bp的区域对人FTZ-F1β基因在Hep G2细胞中的基础转录至关重要。
英文摘要
FTZ-F1β had been implicated to be a counterpart of Ad4BP and mainly expressed in liver and pancreas. We elucidated the structure of the human FTZ-F1β gene. We determined the exonic sequences including the exon/intron baundaries and the sequences at the 5'-flanking region. The gene is at least 50 Kb long and is split into 8 exons including a non-coding exon 1. The overall structural organization of human FTZ-F1β gene was very similar to that of human Ad4BP/SF-1 gene, suggesting that both genes are derived from common ancestor gene. In addition, a preliminary study of transcriptional regulation of human FTZ-F1β gene in Hep G2 cells using a series of deletion analysies of the 5'-flanking region of human FTZ-F1β gene revealed a upstream region of -1743 to -1040 bp from the transcriptional statsite to be essential for the basal transcription of the human FTZ-F1β gene in Hep G2 cells.
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Nawata, H., Yanase, T.et al.: "Human Ad4BP/SF-1 and its related nuclear receptor"J Steroid Biochem Molec. 69. 323-328 (1999)
Nawata, H., Yanase, T.等人:“人类 Ad4BP/SF-1 及其相关核受体”J Steroid Biochem Molec。
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通讯作者:
Oba K,Yanase T et al.: "Transcriptional regulation of human FTZ-F1 gene encoding Ad4BP/SF-1"J Biochem. 128. 517-528 (2000)
Oba K,Yanase T 等人:“编码 Ad4BP/SF-1 的人 FTZ-F1 基因的转录调控”J Biochem。
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通讯作者:
Nawata H, Yanase T et al.: "Human Ad4BP/SF-1 and its velated nuclear receptor" J. Steroid Biochiem Molec. 印刷中. (1999)
Nawata H、Yanase T 等人:“人类 Ad4BP/SF-1 及其相关核受体”J. Steroid Biochiem Molec 出版(1999 年)。
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Hirase N,Yanase T, et al.: "Thiazolidinedione suppresses the expression of erythroid phenotype in erythroleukemia cell line K562."Leukemia Research. 24. 393-400 (2000)
Hirase N、Yanase T 等人:“噻唑烷二酮抑制红白血病细胞系 K562 中红系表型的表达。”白血病研究。
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通讯作者:
Oba K, Yanase T et al.: "Transcriptional regulation of hurman FTZ-F1 gene encoding Ad4BP/SF-1"J Biochem. 128. 517-528 (2000)
Oba K、Yanase T 等人:“编码 Ad4BP/SF-1 的 hurman FTZ-F1 基因的转录调控”J Biochem。
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共 14 条
Research on a novel selective androgen receptor modulator, S42 for the development of life-related drug.
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批准号:23390248
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.31万
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财政年份:2011
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负责人:YANASE Toshihiko
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依托单位:
Basic and clinical research on abnormalities of sexual differentiation associated with synthesis and action of sex steroids
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批准号:16086207
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项目类别:Grant-in-Aid for Scientific Research on Priority Areas
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资助金额:$53.12万
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财政年份:2004
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负责人:YANASE Toshihiko
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依托单位:
Research on the transcriptional regulation of human Ad4BP gene and its related diseases
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批准号:08671171
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.34万
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财政年份:1996
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负责人:YANASE Toshihiko
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依托单位:
海外基金