Abstract: RNA interference (RNAi) provides defense against exogenous nucleic acids, such as viruses and transposons, in diverse organisms. The production of short interfering RNAs (siRNAs) antisense to the viral or transposon sequences is a hallmark of the RNAi response. The discovery of the endogenous antisense siRNAs (endo-siRNAs) matching thousands of protein coding sequences in C. elegans and identification of similar molecules in Drosophila and mammals poses a question about their function. Our recent microarray analysis of genes misregulated in the RNAi pathway mutants in C. elegans revealed preferential targeting by the RNAi components and endogenous short RNAs of genes whose inactivation is beneficial for stress resistance and lifespan extension, such as genes encoding translation factors. We propose that pools of endogenous short RNAs in C. elegans are subject to natural selection. Therefore, the composition of siRNAs in populations is adjusted in response to the environmental changes to achieve maximum fitness. The goal of this project is to test the above model. We will select populations of C. elegans resistant to specific environmental conditions and test these populations for the accumulation of endosiRNAs antisense to very specific genes whose inactivation allows survival under the tested condition. We already established a correlation between thermotolerance and accumulation of endo-siRNAs specific to translation initiation factors. In addition, natural selection for survival on the nematocidal drugs ivermectin and levamisole will be used to generate C. elegans strains resistant to drugs due to epigenetic endo-siRNA-based inactivation of specific genes. Proving the existence of a siRNA-based epigenetic natural selection would represent a fundamental breakthrough in basic science. Epigenetic RNAi-based mechanisms are not likely to be limited to lower organisms and may be involved in the immune escape and drug-resistance of malignant tumors and in other cases when cells evolve to escape the action of therapeutic agents. Public Health Relevance: This project is focused on revealing new mechanisms used by organisms for the adaptation to environment. If we confirm that composition of short RNA molecules in the nematode C. elegans is selected to maximize survival under specific conditions, this will open the doors for """"""""natural selection"""""""" experiments aimed at generation of cells with specific characteristics. For example, neuronal cells with enhanced ability to resist oxidative stress could be generated.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s New Innovator Awards (DP2)
Project #
1DP2OD006412-01
Application #
7840683
Study Section
Special Emphasis Panel (ZGM1-NDIA-O (02))
Program Officer
Basavappa, Ravi
Project Start
2009-09-30
Project End
2014-06-30
Budget Start
2009-09-30
Budget End
2014-06-30
Support Year
1
Fiscal Year
2009
Total Cost
$2,413,250
Indirect Cost
Name
Columbia University (N.Y.)
Department
Biochemistry
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Cecere, Germano; Hoersch, Sebastian; O'Keeffe, Sean et al. (2014) Global effects of the CSR-1 RNA interference pathway on the transcriptional landscape. Nat Struct Mol Biol 21:358-65
Kennedy, Lisa M; Grishok, Alla (2014) Neuronal migration is regulated by endogenous RNAi and chromatin-binding factor ZFP-1/AF10 in Caenorhabditis elegans. Genetics 197:207-20
Cecere, Germano; Grishok, Alla (2014) A nuclear perspective on RNAi pathways in metazoans. Biochim Biophys Acta 1839:223-33
Cecere, Germano; Grishok, Alla (2014) RNA Chromatin Immunoprecipitation (RNA-ChIP) in Caenorhabditis elegans. Bio Protoc 4:
Avgousti, Daphne C; Cecere, Germano; Grishok, Alla (2013) The conserved PHD1-PHD2 domain of ZFP-1/AF10 is a discrete functional module essential for viability in Caenorhabditis elegans. Mol Cell Biol 33:999-1015
Cecere, Germano; Hoersch, Sebastian; Jensen, Morten B et al. (2013) The ZFP-1(AF10)/DOT-1 complex opposes H2B ubiquitination to reduce Pol II transcription. Mol Cell 50:894-907
Cecere, Germano; Zheng, Grace X Y; Mansisidor, Andres R et al. (2012) Promoters recognized by forkhead proteins exist for individual 21U-RNAs. Mol Cell 47:734-45
Avgousti, Daphne C; Palani, Santhosh; Sherman, Yekaterina et al. (2012) CSR-1 RNAi pathway positively regulates histone expression in C. elegans. EMBO J 31:3821-32
Hayward, Douglas G; Wong, Jon W; Zhang, Kai et al. (2011) Multiresidue pesticide analysis in ginseng and spinach by nontargeted and targeted screening procedures. J AOAC Int 94:1741-51
Mansisidor, Andres R; Cecere, Germano; Hoersch, Sebastian et al. (2011) A conserved PHD finger protein and endogenous RNAi modulate insulin signaling in Caenorhabditis elegans. PLoS Genet 7:e1002299

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