pubmed-article:2480959 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0008377 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0034721 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0034693 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0018207 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0010092 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C1330957 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0010762 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0006556 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0085862 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C1299583 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0002518 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C1524075 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0596311 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0439596 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C1608386 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C1549571 | lld:lifeskim |
pubmed-article:2480959 | lifeskim:mentions | umls-concept:C0337112 | lld:lifeskim |
pubmed-article:2480959 | pubmed:issue | 36 | lld:pubmed |
pubmed-article:2480959 | pubmed:dateCreated | 1990-2-1 | lld:pubmed |
pubmed-article:2480959 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:abstractText | We report the isolating and sequencing of three cDNA clones encoding rat P-450scc, the nucleotide and protein sequences of which are highly homologous to those of bovine and human P-450scc, especially in the putative heme and steroid binding domains. We document that different molecular mechanisms regulate P-450scc in granulosa cells of preovulatory (PO) follicles prior to and after luteinization. Luteinizing hormone/human chorionic gonadotropin (LH/hCG) and cAMP are obligatory to induce P-450scc mRNA in PO granulosa cells in vivo and in vitro. Once P-450scc mRNA is induced as a consequence of the LH/hCG surge it is constitutively maintained by luteinized cells in vivo (0-4 days) and in vitro (0-9 days) in the absence of gonadotropins, is susceptible to modulation by prolactin and is no longer regulated by cAMP. Exposure to elevated concentrations of hCG in vivo for 5-7 h was required for PO granulosa cells to undergo a functional transition establishing the stable luteal cell phenotype. Transient exposure of PO + hCG (7 h) follicles in vitro to the RNA synthesis inhibitor actinomycin D (1 microgram/ml) or the protein synthesis inhibitor cycloheximide (10 micrograms/ml), for 1-5 h prior to culturing the granulosa cells failed to disrupt the induction of P-450scc mRNA, progesterone biosynthesis, and appearance of the luteal cell morphology. Inhibitors of protein kinase A (Rp-cAMPS; 1-500 microM and N-[2-(methylamino)ethyl]-5-isoquinolinesulfonamide dihydrochloride (H8); 1-200 microM) added directly to the luteinized cell cultures also failed to alter P-450scc mRNA in these cells, although the cells contain in vivo amounts of mRNA for RII beta, RI alpha, and C alpha, the primary subunits of protein kinase A found in the rat ovary. These data suggest that expression of the P-450scc gene in rat ovarian follicular cells is regulated in a sequential manner by cAMP-dependent and cAMP-independent mechanisms associated with granulosa cells and luteal cells, respectively. | lld:pubmed |
pubmed-article:2480959 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:language | eng | lld:pubmed |
pubmed-article:2480959 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2480959 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2480959 | pubmed:month | Dec | lld:pubmed |
pubmed-article:2480959 | pubmed:issn | 0021-9258 | lld:pubmed |
pubmed-article:2480959 | pubmed:author | pubmed-author:RichardsJ SJS | lld:pubmed |
pubmed-article:2480959 | pubmed:author | pubmed-author:BeattieW GWG | lld:pubmed |
pubmed-article:2480959 | pubmed:author | pubmed-author:KrasnowJ SJS | lld:pubmed |
pubmed-article:2480959 | pubmed:author | pubmed-author:OonkR BRB | lld:pubmed |
pubmed-article:2480959 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2480959 | pubmed:day | 25 | lld:pubmed |
pubmed-article:2480959 | pubmed:volume | 264 | lld:pubmed |
pubmed-article:2480959 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2480959 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2480959 | pubmed:pagination | 21934-42 | lld:pubmed |
pubmed-article:2480959 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:meshHeading | pubmed-meshheading:2480959-... | lld:pubmed |
pubmed-article:2480959 | pubmed:year | 1989 | lld:pubmed |
pubmed-article:2480959 | pubmed:articleTitle | Cyclic AMP-dependent and -independent regulation of cholesterol side chain cleavage cytochrome P-450 (P-450scc) in rat ovarian granulosa cells and corpora lutea. cDNA and deduced amino acid sequence of rat P-450scc. | lld:pubmed |
pubmed-article:2480959 | pubmed:affiliation | Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030. | lld:pubmed |
pubmed-article:2480959 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2480959 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:2480959 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
entrez-gene:29680 | entrezgene:pubmed | pubmed-article:2480959 | lld:entrezgene |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2480959 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2480959 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2480959 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2480959 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2480959 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2480959 | lld:pubmed |