Literature DB >> 16105662

Global gene expression response to telomerase in bovine adrenocortical cells.

Steven D Perrault1, Peter J Hornsby, Dean H Betts.   

Abstract

The infinite proliferative capability of most immortalized cells is dependent upon the presence of the enzyme telomerase and its ability to maintain telomere length and structure. However, telomerase may be involved in a greater system than telomere length regulation, as recent evidence has shown it capable of increasing wound healing in vivo, and improving cellular proliferation rate and survival from apoptosis in vitro. Here, we describe the global gene expression response to ectopic telomerase expression in an in vitro bovine adrenocortical cell model. Telomerase-immortalized cells showed an increased ability for proliferation and survival in minimal essential medium above cells transgenic for GFP. cDNA microarray analyses revealed an altered cell state indicative of increased adrenocortical cell proliferation regulated by the IGF2 pathway and alterations in members of the TGF-B family. As well, we identified alterations in genes associated with development and wound healing that support a model that high telomerase expression induces a highly adaptable, progenitor-like state.

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Year:  2005        PMID: 16105662     DOI: 10.1016/j.bbrc.2005.07.156

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  24 in total

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Review 4.  Regulation of the human catalytic subunit of telomerase (hTERT).

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7.  Evidence of extra-telomeric effects of hTERT and its regulation involving a feedback loop.

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Journal:  Tumour Biol       Date:  2014-01-14

9.  Telomerase reverse transcriptase expression elevated by avian leukosis virus integration in B cell lymphomas.

Authors:  Feng Yang; Rena R Xian; Yingying Li; Tatjana S Polony; Karen L Beemon
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-16       Impact factor: 11.205

10.  Microenvironmental regulation of telomerase isoforms in human embryonic stem cells.

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