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Catalog of mRNA expression patterns for DNA methylating and demethylating genes in developing mouse lower urinary tract
Institution:1. Research Unit, Biomedical Research and Innovation Institute of Cádiz (INiBICA), Puerta del Mar University Hospital, University of Cádiz, Cádiz, Spain;2. Department of Cardiology, Cruz Roja Central Hospital, Madrid, Spain;3. Alfonso X University (UAX), Madrid, Spain;4. Department of Cardiology, Puerta del Mar Universitary Hospital, Cádiz, Spain;5. Department of Pediatric Cardiology, Sant Joan de Déu Hospital, Barcelona, Spain;6. Department of Cardiology, Virgen del Rocio Universitary Hospital, Sevilla, Spain;7. Institute of Biomedical Research of Barcelona (IIBB) - Spanish National Research Council (CSIC), Barcelona, Spain;8. Biomedical Research Institute Sant Pau (IIB Sant Pau), Barcelona, Spain;9. CIBERCV, Institute of Health Carlos III, Madrid, Spain;10. Department of Internal Medicine, Puerta del Mar Universitary Hospital, Cádiz, Spain;11. Department of Medicine, School of Medicine, University of Cádiz, Cádiz, Spain
Abstract:The mouse prostate develops from a component of the lower urinary tract (LUT) known as the urogenital sinus (UGS). This process requires androgens and signaling between mesenchyme and epithelium. Little is known about DNA methylation during prostate development, including which factors are expressed, whether their expression changes over time, and if DNA methylation contributes to androgen signaling or influences signaling between mesenchyme and epithelium. We used in situ hybridization to evaluate the spatial and temporal expression pattern of mRNAs which encode proteins responsible for establishing, maintaining or remodeling DNA methylation. These include DNA methyltrasferases, DNA deaminases, DNA glycosylases, base excision repair and mismatch repair pathway members. The mRNA expression patterns were compared between male and female LUT prior to prostatic bud formation (14.5 days post coitus (dpc)), during prostatic bud formation (17.5 dpc) and during prostatic branching morphogenesis (postnatal day (P) 5). We found dramatic changes in the patterns of these mRNAs over the course of prostate development and identified examples of sexually dimorphic mRNA expression. Future investigation into how DNA methylation patterns are established, maintained and remodeled during the course of embryonic prostatic bud formation may provide insight into prostate morphogenesis and disease.
Keywords:Urogenital sinus  Lower urinary tract  Prostate  Epigenetics  DNA methylation  DNA demethylation  LUT"}  {"#name":"keyword"  "$":{"id":"k0040"}  "$$":[{"#name":"text"  "_":"lower urinary tract  UGS"}  {"#name":"keyword"  "$":{"id":"k0050"}  "$$":[{"#name":"text"  "_":"urogenital sinus  dpc"}  {"#name":"keyword"  "$":{"id":"k0060"}  "$$":[{"#name":"text"  "_":"days post coitus  P"}  {"#name":"keyword"  "$":{"id":"k0070"}  "$$":[{"#name":"text"  "_":"postnatal day  AR"}  {"#name":"keyword"  "$":{"id":"k0080"}  "$$":[{"#name":"text"  "_":"androgen receptor  ISH"}  {"#name":"keyword"  "$":{"id":"k0090"}  "$$":[{"#name":"text"  "$$":[{"#name":"italic"  "_":"in situ"}  {"#name":"__text__"  "_":" hybridization  IHC"}  {"#name":"keyword"  "$":{"id":"k0100"}  "$$":[{"#name":"text"  "_":"immunohistochemistry
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