Jump to: Page Content, Section Navigation, Site Navigation, Site Search, Account Information, or Site Tools.
|
|
Supplementary MaterialSupplemental Figure 1. TAF 105-/- ovaries are significantly smaller than matched TAF 105+/- ovaries. Ovaries from heterozygous and homozygous-null 12-week-old siblings were dissected and viewed concurrently by light microscopy with an Olympus SZH10 microscope.
Medium version | Full size version
Supplemental Figure 2. Comprehensive results of microarray data indicating genes that were designated decreased or increased twofold or greater in the TAFII105 mutant ovaries. Of over 13,000 probe sets tested on Affymetrix murine 11K arrays, only 309 genes fit such criteria. 132 genes are designated D or MD for decrease or marginally decrease, respectively. In addition, 177 genes are designated I or MI for increase or marginally increase, respectively. Probe sets represent Genbank accesion numbers or Msa numbers designated by Affymetrix. All data analysis was completed using microarray suite version 4.0 from Affymetrix.
Supplemental Figure 3. Model of TAFII105-mediated transcriptional activation in the ovary. Granulosa cell activator proteins (labeled G.C. Act.) expressed in granulosa cells of the developing follicle recruit TFIID to the core promoter of selective target genes. We postulate that this is accomplished through specific protein-protein interactions between activators (shown in yellow) and the TAFII105 (shown in red) subunit of TFIID. Activation of the specific pathways and genes that have previously been implicated in folliculogenesis (shown by the arrows) requires TAFII105 (see text). In the absence of TAFII105, transcription of these select target genes is compromised leading to an arrest of folliculogenesis and female sterility in the TAFII105-null mice.
Medium version | Full size version
|
Science. ISSN 0036-8075 (print), 1095-9203 (online)