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鸡FTZ-F1相关孤儿受体的分子克隆

Molecular cloning of chicken FTZ-F1-related orphan receptors.

作者信息

Kudo T, Sutou S

机构信息

Central Research Institute, Itoham Foods Inc., Ibaraki, Japan.

出版信息

Gene. 1997 Sep 15;197(1-2):261-8. doi: 10.1016/s0378-1119(97)00270-9.

DOI:10.1016/s0378-1119(97)00270-9
PMID:9332374
Abstract

FTZ-F1 is a member of the orphan nuclear receptors, which belongs to the steroid hormone receptor superfamily, and plays a role in the blastoderm and nervous system development in Drosophila. Recently, several FTZ-F1 family genes have been cloned in several species. SF-1/Ad4BPs have been identified as master regulators controlling steroidogenic P-450 genes in mammals and are considered to be the mammalian homologues of FTZ-F1. Moreover, SF-1/Ad4BP plays a critical role in the sexual differentiation of gonads in mammals. In vertebrates, except for mammals, the functional homologue of SF-1/Ad4BP has not been identified before. Herein, we cloned two chicken cDNAs (OR2.0 and OR2.1), which encode putative FTZ-F1 family receptors, by reverse transcriptase-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE). OR2.1 consists of 3255 bp, is expressed in the adrenal glands and gonads, and is considered to be the chicken counterpart of mammalian SF-1/Ad4BP. However, OR2.0 consists of 2945 bp, is expressed in the livers and the adrenal glands, and is considered to be the chicken counterpart of mouse LRH-1, which is a member of the FTZ-F1 family in mammals.

摘要

FTZ - F1是孤儿核受体家族的成员,属于类固醇激素受体超家族,在果蝇的胚盘和神经系统发育中发挥作用。最近,在多个物种中克隆出了几个FTZ - F1家族基因。SF - 1/Ad4BPs已被确定为哺乳动物中控制类固醇生成性P - 450基因的主要调节因子,并被认为是FTZ - F1的哺乳动物同源物。此外,SF - 1/Ad4BP在哺乳动物性腺的性别分化中起关键作用。在脊椎动物中,除了哺乳动物外,此前尚未鉴定出SF - 1/Ad4BP的功能同源物。在此,我们通过逆转录聚合酶链反应(RT - PCR)和cDNA末端快速扩增(RACE)克隆了两个鸡的cDNA(OR2.0和OR2.1),它们编码推定的FTZ - F1家族受体。OR2.1由3255个碱基对组成,在肾上腺和性腺中表达,被认为是哺乳动物SF - 1/Ad4BP的鸡对应物。然而,OR2.0由2945个碱基对组成,在肝脏和肾上腺中表达,被认为是小鼠LRH - 1的鸡对应物,小鼠LRH - 1是哺乳动物FTZ - F1家族的成员。

相似文献

1
Molecular cloning of chicken FTZ-F1-related orphan receptors.鸡FTZ-F1相关孤儿受体的分子克隆
Gene. 1997 Sep 15;197(1-2):261-8. doi: 10.1016/s0378-1119(97)00270-9.
2
Molecular cloning and expression of the SF-1/Ad4BP gene in the frog, Rana rugosa.日本皱蛙中SF-1/Ad4BP基因的分子克隆与表达
Gene. 1998 Nov 19;222(2):169-76. doi: 10.1016/s0378-1119(98)00498-3.
3
Characterization of the shrimp eyestalk cDNA encoding a novel fushi tarazu-factor 1 (FTZ-F1).对编码一种新型分节基因因子1(FTZ-F1)的虾眼柄cDNA的表征。
FEBS Lett. 1999 Jul 2;454(1-2):109-14. doi: 10.1016/s0014-5793(99)00787-5.
4
cDNA cloning and mRNA expression of a FTZ-F1 homologue from the pituitary of the orange-spotted grouper, epinephelus coioides.斜带石斑鱼垂体中一种FTZ-F1同源物的cDNA克隆及mRNA表达
J Exp Zool A Comp Exp Biol. 2004 Aug 1;301(8):691-9. doi: 10.1002/jez.a.74.
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Transcriptional regulation of the human FTZ-F1 gene encoding Ad4BP/SF-1.编码Ad4BP/SF-1的人类FTZ-F1基因的转录调控
J Biochem. 2000 Sep;128(3):517-28. doi: 10.1093/oxfordjournals.jbchem.a022782.
6
cDNA cloning of a new member of the FTZ-F1 subfamily from a rainbow trout.从虹鳟鱼中克隆FTZ-F1亚家族一个新成员的cDNA
Biochim Biophys Acta. 1998 Feb 11;1395(3):271-4. doi: 10.1016/s0167-4781(97)00158-9.
7
FTZ-F1alpha is expressed in the developing gonad of frogs.FTZ-F1α 在青蛙发育中的性腺中表达。
Biochim Biophys Acta. 2000 Nov 15;1494(1-2):195-200. doi: 10.1016/s0167-4781(00)00201-3.
8
Structural characterization of the chicken SF-1/Ad4BP gene.
Gene. 1999 Apr 29;231(1-2):33-40. doi: 10.1016/s0378-1119(99)00097-9.
9
Ad4BP regulating steroidogenic P-450 gene is a member of steroid hormone receptor superfamily.调控类固醇生成性P-450基因的Ad4BP是类固醇激素受体超家族的成员。
J Biol Chem. 1993 Apr 5;268(10):7494-502.
10
An E box element is required for the expression of the ad4bp gene, a mammalian homologue of ftz-f1 gene, which is essential for adrenal and gonadal development.E盒元件是ad4bp基因表达所必需的,ad4bp基因是ftz-f1基因的哺乳动物同源物,对肾上腺和性腺发育至关重要。
J Biol Chem. 1995 Mar 31;270(13):7453-61. doi: 10.1074/jbc.270.13.7453.

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Mol Cell Biol. 2003 Oct;23(19):6713-24. doi: 10.1128/MCB.23.19.6713-6724.2003.
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Zebrafish ftz-f1 gene has two promoters, is alternatively spliced, and is expressed in digestive organs.斑马鱼ftz-f1基因有两个启动子,存在可变剪接,且在消化器官中表达。
Biochem J. 2000 Jun 1;348 Pt 2(Pt 2):439-46.