Abstract
The level of green fluorescent protein expression from an hsp-16.2-based transcriptional reporter predicts life span and thermotolerance in Caenorhabditis elegans. The initial report used a high-copy number reporter integrated into chromosome IV. There was concern that the life-span prediction power of this reporter was not attributable solely to hsp-16.2 output. Specifically, prediction power could stem from disruption of some critical piece of chromatin on chromosome IV by the gpIs1 insertion, a linked mutation from the process used to create the reporter, or from an artifact of transgene regulation (multicopy transgenes are subject to regulation by C elegans chromatin surveillance machinery). Here we determine if the ability to predict life span and thermotolerance is specific to the gpIs1 insertion or a general property of hsp-16.2-based reporters. New single-copy hsp-16.2-based reporters predict life span and thermotolerance. We conclude that prediction power of hsp-16.2-based transcriptional reporters is not an artifact of any specific transgene configuration or chromatin surveillance mechanism. © 2012 The Gerontological Society of America.
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Mendenhall, A. R., Tedesco, P. M., Taylor, L. D., Lowe, A., Cypser, J. R., & Johnson, T. E. (2012). Expression of a single-copy hsp-16.2 reporter predicts life span. Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 67 A(7), 726–733. https://doi.org/10.1093/gerona/glr225
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