E-MTAB-120 - Transcription profiling of mouse pancreatic islets on day 14.5 of pregnancy

Submitted on 26 June 2009, released on 5 August 2009, last updated on 3 May 2014
Mus musculus
Samples (8)
Array (1)
Protocols (7)
The inability of the beta-cell to meet the demand for insulin brought about by insulin resistance leads to type 2 diabetes. In adults, beta-cell replication is one of the mechanisms thought to cause the expansion of beta-cell mass. Efforts to treat diabetes require knowledge of the pathways that drive facultative beta-cell proliferation in vivo. A robust physiological stimulus of beta-cell expansion is pregnancy, and identifying the mechanisms underlying this stimulus may provide therapeutic leads for the treatment of type 2 diabetes. The peak in beta-cell proliferation during pregnancy occurs on day 14.5 of gestation in mice. Using advanced genomic approaches, we globally characterize the gene expression signature of pancreatic islets on day 14.5 of gestation during pregnancy. We identify a total of 1,907 genes as differentially expressed in the islet during pregnancy. We demonstrate that the islet's ability to compensate for relative insulin deficiency during metabolic stress is associated with the induction of both proliferative and survival pathways. A comparison of the genes induced in three different models of islet expansion suggests that diverse mechanisms can be recruited to expand islet mass. The identification of many novel genes involved in islet expansion during pregnancy provides an important resource for diabetes researchers to further investigate how these factors contribute to the maintenance of not only islet mass, but ultimately beta-cell mass.
Experiment types
transcription profiling by array, development or differentiation,co-expression
The Transcriptional Response of the Islet to Pregnancy in Mice. Rieck, Sebastian; White, Peter; Schug, Jonathan; Fox, Alan J.; Smirnova, Olga; Gao, Nan; Gupta, Rana K.; Wang, Zhao V.; Scherer, Philipp E.; Keller, Mark P.; Attie, Alan D.; Kaestner, Klaus H. , Europe PMC 19574445
Investigation descriptionE-MTAB-120.idf.txt
Sample and data relationshipE-MTAB-120.sdrf.txt
Raw data (1)E-MTAB-120.raw.1.zip
Processed data (2)E-MTAB-120.processed.1.zip, E-MTAB-120.processed.2.zip
Array designA-MEXP-724.adf.txt
R ExpressionSetE-MTAB-120.eSet.r