J. Smith at Baylor has shown that when poly(A)+ RNA derived from human diploid fibroblasts at late passage is microinjected into the same cell type at early passage, the growth of the early passage cells is halted. A functionally identical activity derived from rat liver (by K. McClung and J. Smith) has a single molecular weight peak of activity on sucrose gradients. These data suggest that a single messenger RNA has the ability to shut off cell growth, and dilution experiments suggest that the message is abundant (1/100-1/1000 of total message). We are attempting to clone this mRNA by two different methods: 1) hybrid selection screening of a cDNA library, and 2) construction of a cDNA library in a T7 vector that should permit us to make synthetic mRNAs that can be tested directly by microinjection.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Intramural Research (Z01)
Project #
1Z01AG000705-04
Application #
3817649
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Aging
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Sharov, Alexei A; Falco, Geppino; Piao, Yulan et al. (2008) Effects of aging and calorie restriction on the global gene expression profiles of mouse testis and ovary. BMC Biol 6:24
Zahn, Jacob M; Poosala, Suresh; Owen, Art B et al. (2007) AGEMAP: a gene expression database for aging in mice. PLoS Genet 3:e201