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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">mouse</item><item key="factors"><item><item key="GSM468776"><item key="GENOTYPE">Wild-type</item></item></item><item><item key="GSM468776"><item key="GENOTYPE">Wild-type</item></item></item><item><item key="GSM468778"><item key="GENOTYPE">Cnot3 heterozygotes</item></item></item><item><item key="GSM468778"><item key="GENOTYPE">Cnot3 heterozygotes</item></item></item></item><item key="id">5887</item><item key="pop_total">0</item><item key="platform">6</item><item key="summary_wrapped">Decay of mRNAs initiates with shortening of the poly(A) tail. Although the CCR4-NOT complex participates in deadenylation, how it becomes...</item><item key="geo_gse_id">E-GEOD-18924</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">4</item><item key="tags"><item>glucose</item><item>lipid</item><item>liver</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-18924_A-AFFY-45</item><item key="slug">expression-data-from-the-liver-of-wild-type-and-cn</item><item key="geo_gds_id"/><item key="name">Expression data from the liver of wild-type and Cnot3+/- mice: Fasted</item><item key="created">Nov.11, 2014</item><item key="summary">Decay of mRNAs initiates with shortening of the poly(A) tail. Although the CCR4-NOT complex participates in deadenylation, how it becomes activates remain obscure. We show that complete deficiency in CNOT3, subunit 3 of this complex, is lethal in mice, but that heterozygotes survive as lean mice with hepatic and adipose tissues containing reduced lipid levels. Cnot3+/- mice have enhanced metabolic rates and remain lean on high-fat diets. To examine the underlying mechanisms by which CNOT3 is involved in the control of metabolic balance, we compared the gene expression profiles of wild-type and Cnot3+/- mice using Affymetrix microarray technology. We chose to analyze the liver because the CNOT3 level in the liver was affected by the feeding condition and because the liver plays a major role in glucose and lipid metabolism. The livers were isolated from 12-week-old wild-type and Cnot3+/- mice (n = 2 for each genotype).</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-18924</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-18924/samples/</item></data></biogps>
