Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1993-2-26
pubmed:abstractText
Examination of the regulation of prodynorphin (pro-DYN) promoter activity is limited by the absence of a good cell model. The discovery of pro-DYN mRNA and derived peptides in the reproductive tract led us to examine the cellular localization and hormonal regulation of ovarian pro-DYN expression and to evaluate normal granulosa cells as a model for studying pro-DYN gene regulation. Ovarian pro-DYN mRNA levels were significantly elevated in PMSG-primed immature rats 12-24 h after receiving an ovulatory dose of hCG. Levels peaked 2 days after hCG, remained elevated throughout the ensuing pseudopregnancy, and rose again at the end of pseudopregnancy. In situ hybridization localized pro-DYN expression predominantly to granulosa and luteal cells. Transfection of primary cultures of granulosa cells revealed that the activity of the rat pro-DYN promoter [-1858 to 133 base pairs (bp)] was increased 18- to 19-fold by hCG and human FSH treatments and 7-fold by cAMP analog treatment. Deletion analysis identified a 358 bp fragment as the primary hormone-responsive sequence (-1858 to -1500 bp; containing three potential cAMP-responsive elements); its deletion resulted in severely reduced FSH responsiveness, and its ligation to hormone-unresponsive basal promoter sequences completely restored FSH responsiveness. This is an unusually distal position for cAMP-responsive elements compared to other cAMP-regulated genes. These data demonstrate specific expression of pro-DYN in granulosa and luteal cells, which is under sensitive gonadotropin regulation, and identify a distal hormone-responsive sequence within the promoter.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0888-8809
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2244-56
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:1337148-Animals, pubmed-meshheading:1337148-Base Sequence, pubmed-meshheading:1337148-Cells, Cultured, pubmed-meshheading:1337148-Chorionic Gonadotropin, pubmed-meshheading:1337148-Cyclic AMP, pubmed-meshheading:1337148-DNA, pubmed-meshheading:1337148-Enkephalins, pubmed-meshheading:1337148-Female, pubmed-meshheading:1337148-Follicle Stimulating Hormone, pubmed-meshheading:1337148-Gene Expression Regulation, pubmed-meshheading:1337148-Gonadotropins, Equine, pubmed-meshheading:1337148-Granulosa Cells, pubmed-meshheading:1337148-In Situ Hybridization, pubmed-meshheading:1337148-Molecular Sequence Data, pubmed-meshheading:1337148-Ovary, pubmed-meshheading:1337148-Ovulation Induction, pubmed-meshheading:1337148-Promoter Regions, Genetic, pubmed-meshheading:1337148-Protein Precursors, pubmed-meshheading:1337148-Rats, pubmed-meshheading:1337148-Rats, Sprague-Dawley, pubmed-meshheading:1337148-Recombinant Fusion Proteins, pubmed-meshheading:1337148-Regulatory Sequences, Nucleic Acid, pubmed-meshheading:1337148-Sequence Homology, Nucleic Acid, pubmed-meshheading:1337148-Transfection
pubmed:year
1992
pubmed:articleTitle
Regulation of prodynorphin gene expression in the ovary: distal DNA regulatory elements confer gonadotropin regulation of promoter activity.
pubmed:affiliation
Division of Reproductive Biology, Oregon Regional Primate Research Center, Beaverton 97006.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.