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孕酮受体:修订间差异

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2014年6月28日 (六) 15:15的版本

Progesterone receptor
孕酮受体
PDB rendering based on 1a28.
有效结构
PDB 直系同源检索:PDBe, RCSB
标识
代号 PGR; NR3C3; PR
扩展标识 遗传学607311 鼠基因97567 同源基因713 IUPHAR:   ChEMBL: 208 GeneCards: PGR Gene
RNA表达模式
更多表达数据
直系同源体
物种 人类 小鼠
Entrez 5241 18667
Ensembl ENSG00000082175 ENSMUSG00000031870
UniProt P06401 n/a
mRNA序列 NM_000926 NM_008829
蛋白序列 NP_000917 NP_032855
基因位置 Chr 11:
100.9 – 101 Mb
Chr 9:
8.9 – 8.97 Mb
PubMed查询 [1] [2]

孕酮受体(英語:progesterone receptor,缩写PR,也被称为NR3C3 ,nuclear receptor subfamily 3, group C, member 3,即核受体第三亚族C组成员3)是一种细胞内蛋白质,由甾体激素孕酮激活。

In humans, PR is encoded by a single PGR gene residing on chromosome 11q22,[1][2][3] it has two main forms, A and B, that differ in their molecular weight.[4][5][6]

功能

Progesterone is necessary to induce the progesterone receptors. When no binding hormone is present the carboxyl terminal inhibits transcription. Binding to a hormone induces a structural change that removes the inhibitory action. Progesterone antagonists prevent the structural reconfiguration.

After progesterone binds to the receptor, restructuring with dimerization follows and the complex enters the nucleus and binds to DNA. There transcription takes place, resulting in formation of messenger RNA that is translated by ribosomes to produce specific proteins.

结构

Progesterone receptor, N-terminal
鑑定
標誌Progest_rcpt_N
PfamPF02161旧版
InterPro英语InterProIPR000128

In common with other steroid receptors, the progesterone receptor has a N-terminal regulatory domain, a DNA binding domain, a hinge section, and a C-terminal ligand binding domain. A special transcription activation function (TAF), called TAF-3, is present in the progesterone receptor-B, in a B-upstream segment (BUS) at the amino acid terminal. This segment is not present in the receptor-A.

互作

孕酮受体has been shown to interact with:

另见

参考文献

  1. ^ Misrahi M, Atger M, d'Auriol L, Loosfelt H, Meriel C, Fridlansky F, Guiochon-Mantel A, Galibert F, Milgrom E. Complete amino acid sequence of the human progesterone receptor deduced from cloned cDNA. Biochem. Biophys. Res. Commun. March 1987, 143 (2): 740–8. PMID 3551956. doi:10.1016/0006-291X(87)91416-1. 
  2. ^ Law ML, Kao FT, Wei Q, Hartz JA, Greene GL, Zarucki-Schulz T, Conneely OM, Jones C, Puck TT, O'Malley BW. The progesterone receptor gene maps to human chromosome band 11q13, the site of the mammary oncogene int-2. Proc. Natl. Acad. Sci. U.S.A. May 1987, 84 (9): 2877–81. PMC 304763可免费查阅. PMID 3472240. doi:10.1073/pnas.84.9.2877. 
  3. ^ ensembl.org, Gene: ESR1 (ENSG00000091831)
  4. ^ Gadkar-Sable S, Shah C, Rosario G, Sachdeva G, Puri C. Progesterone receptors: various forms and functions in reproductive tissues. Front. Biosci. 2005, 10: 2118–30. PMID 15970482. doi:10.2741/1685. 
  5. ^ Kase, Nathan G.; Speroff, Leon; Glass, Robert L. Clinical gynecologic endocrinology and infertility. Hagerstown, MD: Lippincott Williams & Wilkins. 1999. ISBN 0-683-30379-1. 
  6. ^ Fritz, Marc A.; Speroff, Leon. Clinical gynecologic endocrinology and infertility. Hagerstown, MD: Lippincott Williams & Wilkins. 2005. ISBN 0-7817-4795-3. 
  7. ^ Zhang XL, Zhang D, Michel FJ, Blum JL, Simmen FA, Simmen RC. Selective interactions of Kruppel-like factor 9/basic transcription element-binding protein with progesterone receptor isoforms A and B determine transcriptional activity of progesterone-responsive genes in endometrial epithelial cells. J. Biol. Chem. June 2003, 278 (24): 21474–82. PMID 12672823. doi:10.1074/jbc.M212098200. 
  8. ^ Giangrande PH, Kimbrel EA, Edwards DP, McDonnell DP. The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding. Mol. Cell. Biol. May 2000, 20 (9): 3102–15. PMC 85605可免费查阅. PMID 10757795. doi:10.1128/MCB.20.9.3102-3115.2000. 
  9. ^ Nawaz Z, Lonard DM, Smith CL, Lev-Lehman E, Tsai SY, Tsai MJ, O'Malley BW. The Angelman syndrome-associated protein, E6-AP, is a coactivator for the nuclear hormone receptor superfamily. Mol. Cell. Biol. February 1999, 19 (2): 1182–9. PMC 116047可免费查阅. PMID 9891052. 

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外部链接

此条目包含有源于Pfam以及InterPro的属于公有领域的文本 IPR000342