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Citation Luo S, Kleemann GA, Ashraf JM, Shaw WM, Murphy CT. TGF- and insulin signaling regulate reproductive aging via oocyte and germline quality maintenance. Cell, 2010.
PubMed ID 20946987
Short Description TGF- and insulin signaling regulate reproductive aging via oocyte and germline quality maintenance.
GEO Record: GSE23446 GSE23447 GSE23448 GSE23509 Platform: GPL7727
Download gene-centric, log2 transformed data: WBPaper00037682.ce.mr.csv
# of Conditions 17
Full Description 1316625150_help Reproductive cessation is perhaps the earliest aging phenotype that humans experience. Similarly, reproduction of Caenorhabditis elegans ceases in mid-adulthood. Although somatic aging has been studied in both worms and humans, mechanisms regulating reproductive aging are not yet understood. Here, we show that TGF- Sma/Mab and Insulin/IGF-1 signaling regulate C. elegans reproductive aging by modulating multiple aspects of the reproductive process, including embryo integrity, oocyte fertilizability, chromosome segregation fidelity, DNA damage resistance, and oocyte and germline morphology. TGF- activity regulates reproductive span and germline/oocyte quality noncell-autonomously and is temporally and transcriptionally separable from its regulation of growth. Chromosome segregation, cell cycle, and DNA damage response genes are upregulated in TGF- mutant oocytes, decline in aged mammalian oocytes, and are critical for oocyte quality maintenance. Our data suggest that C. elegans and humans share many aspects of reproductive aging, including the correlation between reproductive aging and declining oocyte quality and mechanisms determining oocyte quality.
Experimental Details:
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep1_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep2_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep3_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep4_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep5_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep6_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep8_SL2.6.09
WBPaper00037682:sma-2;fem-1_oocyte_D8_vs_fem-1_oocyte_D8_rep9_SL2.6.09
WBPaper00037682:sma-2x3_L4_vs_N2_L4_rep1_WS_4.6.07
WBPaper00037682:N2_L4_vs_sma-2x3_L4_rep2_DF_WS_4.6.07
WBPaper00037682:sma-2x3_L4_vs_N2_L4_rep3_WS_4.6.07
WBPaper00037682:sma-4(e729)_L4_vs_N2_L4_rep1_WS_4.10.7
WBPaper00037682:fem-1_oocyte_D3_vs_fem-1_oocyte_D8_rep3_SL9.13.08
WBPaper00037682:fem-1_oocyte_D3_vs_fem-1_oocyte_D8_rep5_SL12.02.08
WBPaper00037682:fem-1_oocyte_D3_vs_fem-1_oocyte_D8_rep6_SL12.02.08
WBPaper00037682:fem-1_oocyte_D3_vs_fem-1_oocyte_D8_rep7_SL12.02.08
WBPaper00037682:fem-1_oocyte_D3_vs_fem-1_oocyte_D8_rep8_SL12.02.08.
Tags 1316625150_help
Method: microarray, Species: Caenorhabditis elegans, Tissue Specific: germline, Topic: aging