Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Gene expression differences between TAF4b-KO, Het and WT ovaries at 3 weeks of age


ABSTRACT: The rapid decline of ovarian function in TAF4b-null mice begins in early postnatal life and follicle depletion is completed by sixteen weeks. To uncover differences in gene expression that may underlie accelerated ovarian aging, we compared genome-wide expression profiles of three week old, pre-pubescent TAF4b-null and wild-type ovaries. Total RNA from 9, 3-week-old mice (3 wild-type, 3 TAF4b-heterozygous, 3 TAF4b-null) was obtained as described as above. RNA quality was checked using a Bioanalyzer, and concentration determined using a Nanodrop. 300 ng of each RNA sample was used in the Affymetrix Whole-transcript Sense Target Labeling Assay (Rev 3) followed by hybridization to a GeneChip® Mouse Gene 1.0 ST Array. 9 GeneChips were used to provide biological triplicates of each genotype. The Affymetrix Expression Console (v 1.1) was used to normalize data and determine signal intensity (RMA-Sketch).

ORGANISM(S): Mus musculus

SUBMITTER: Lindsay Lovasco 

PROVIDER: E-GEOD-15228 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Accelerated ovarian aging in the absence of the transcription regulator TAF4B in mice.

Lovasco Lindsay A LA   Seymour Kimberly A KA   Zafra Kathleen K   O'Brien Colin W CW   Schorl Christoph C   Freiman Richard N RN  

Biology of reproduction 20090814 1


The mammalian ovary is unique in that its reproductive life span is limited by oocyte quantity and quality. Oocytes are recruited from a finite pool of primordial follicles that are usually exhausted from the ovary during midadult life. If regulation of this pool is perturbed, the reproductive capacity of the ovary is compromised. TAF4B is a gonad-enriched subunit of the TFIID complex required for female fertility in mice. Previous characterization of TAF4B-deficient ovaries revealed several rep  ...[more]

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