Source:http://linkedlifedata.com/resource/pubmed/id/14631120
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0025936,
umls-concept:C0033371,
umls-concept:C0035696,
umls-concept:C0037663,
umls-concept:C0344315,
umls-concept:C0392762,
umls-concept:C0444706,
umls-concept:C0547070,
umls-concept:C0599894,
umls-concept:C1511790,
umls-concept:C1521840,
umls-concept:C1708248,
umls-concept:C2599577
|
pubmed:issue |
6 Pt 2
|
pubmed:dateCreated |
2003-11-21
|
pubmed:abstractText |
We previously reported that transgenic ablation of gonadotrophs results in impaired development of cells immunostainable for prolactin (PRL) but not of cells immunostainable for growth hormone (GH) or pro-opiomelanocortin (POMC) in pituitary of newborn mice. The question remained whether this reduction in PRL protein is a reflection of reduced PRL mRNA expression, or whether this regulation is only situated at the translational level. We therefore generated a new series of transgenic mice in which gonadotrophs were ablated by diphtheria toxin A targeting, and analyzed hormone mRNA levels instead of hormone protein around the day of birth. Pituitary mRNA expression levels of luteinizing hormone-beta (LHbeta), PRL and GH were quantified using real-time TaqMan RT-PCR. Of the 13 transgenic mice obtained, 8 showed a clear-cut reduction (ranging from 62 to 98%) in LHbeta mRNA levels. PRL mRNA values were significantly reduced in the transgenic mice (p = 0.0034), while GH mRNA expression was unaffected (p = 0.93). An additional observation was that female newborn mice produce 5 times more LHbeta mRNA than male mice whereas no sex difference was observed for expression levels of PRL and GH mRNA. Moreover, in the wild-type mice, LHbeta mRNA expression was 20-fold higher than GH mRNA expression which in turn was 500- to 1,000-fold higher than PRL mRNA expression, suggesting a low expression level of the PRL gene at birth. In conclusion, the present data support the hypothesis that embryonic development of PRL gene expression is stimulated by gonadotrophs.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
1021-7770
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright 2003 National Science Council, ROC and S. Karger AG, Basel
|
pubmed:issnType |
Print
|
pubmed:volume |
10
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
805-12
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:14631120-Animals,
pubmed-meshheading:14631120-DNA Primers,
pubmed-meshheading:14631120-Female,
pubmed-meshheading:14631120-Gene Expression Regulation, Developmental,
pubmed-meshheading:14631120-Growth Hormone,
pubmed-meshheading:14631120-Luteinizing Hormone,
pubmed-meshheading:14631120-Male,
pubmed-meshheading:14631120-Mice,
pubmed-meshheading:14631120-Mice, Transgenic,
pubmed-meshheading:14631120-Paracrine Communication,
pubmed-meshheading:14631120-Pituitary Gland, Anterior,
pubmed-meshheading:14631120-Prolactin,
pubmed-meshheading:14631120-Reverse Transcriptase Polymerase Chain Reaction
|
pubmed:articleTitle |
Targeted ablation of gonadotrophs in transgenic mice depresses prolactin but not growth hormone gene expression at birth as measured by quantitative mRNA detection.
|
pubmed:affiliation |
Department of Molecular Cell Biology, Laboratory of Cell Pharmacology, University of Leuven (K.U. Leuven), Medical School, Campus Gasthuisberg (O & N), BE-3000 Leuven, Belgium. Hugo.Vankelecom@med.kuleuven.ac.be
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|