Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractVariations in the emissions of volatile organic compounds from the toner for a specific photocopier    Next AbstractThe primary structure of aphrodisin »

Dev Growth Differ


Title:Targeted disruption of the murine Plag1 proto-oncogene causes growth retardation and reduced fertility
Author(s):Hensen K; Braem C; Declercq J; Van Dyck F; Dewerchin M; Fiette L; Denef C; Van de Ven WJ;
Address:"Laboratory for Molecular Oncology, Department of Human Genetics, University of Leuven and Flanders Interuniversity Institute for Biotechnology (VIB), Herestraat 49, B-3000 Leuven, Belgium"
Journal Title:Dev Growth Differ
Year:2004
Volume:46
Issue:5
Page Number:459 - 470
DOI: 10.1111/j.1440-169x.2004.00762.x
ISSN/ISBN:0012-1592 (Print) 0012-1592 (Linking)
Abstract:"The pleomorphic adenoma gene 1 (Plag1) proto-oncogene encodes a transcription factor and is implicated in human tumorigenesis via ectopic overexpression. No information is available about its developmental role. To address this, a Plag1-/- mouse strain was generated and it appears that Plag1-deficient mice are viable. No anatomical differences are obvious at birth, except that the weight of Plag1-/- mice is significantly lower in comparison to control litter mates. This early growth retardation is maintained throughout adult life with proportionally smaller organs except for the disproportionally small seminal vesicles and ventral prostate; however, plasma testosterone levels in males were not affected. Furthermore, fertility of both male and female Plag1-/- is reduced. Northern blot analysis revealed that Plag1 is developmentally regulated with high overall fetal expression levels, which drop after birth. Furthermore, Plag1 is differentially expressed and is readily detectable in the reproductive organs and pituitary. Expression of growth regulatory Igf2, a known target gene of Plag1 in tumorigenesis, was not affected in Plag1-/- embryos and pups. The general morphology and histology of the size-reduced pituitaries was not affected. Our results establish that Plag1 disruption in mouse differentially affects pre- and postnatal growth and development of organs, with reproductive repercussions"
Keywords:"Animals Base Sequence Blotting, Northern DNA Primers DNA-Binding Proteins/genetics/*physiology Embryonic Development/genetics Fertility/*genetics Growth/*genetics Immunohistochemistry Insulin-Like Growth Factor II/genetics Mice Mice, Knockout Pituitary Gl;"
Notes:"MedlineHensen, Karen Braem, Caroline Declercq, Jeroen Van Dyck, Frederik Dewerchin, Mieke Fiette, Laurence Denef, Carl Van de Ven, Wim J M eng Research Support, Non-U.S. Gov't Japan 2004/12/21 Dev Growth Differ. 2004 Oct; 46(5):459-70. doi: 10.1111/j.1440-169x.2004.00762.x"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 23-11-2024