Research Topics
| David J GarfinkelSummaryAffiliation: National Cancer Institute Country: USA Publications
| Collaborators
|
Detail Information
Publications
Functional profiling of the Saccharomyces cerevisiae genomeGuri Giaever
Stanford Genome Technology Center, Stanford University, Palo Alto, California 94304, USA
Nature 418:387-91. 2002..Our results validate the yeast gene-deletion collection as a valuable resource for functional genomics...
Post-transcriptional cosuppression of Ty1 retrotranspositionDavid J Garfinkel
Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute, Frederick, Maryland 21702 1201, USA
Genetics 165:83-99. 2003..Furthermore, a decrease in the synthesis of Ty1 cDNA is strongly associated with Ty1 CNC. Together our results suggest that Ty1 cosuppression can occur post-transcriptionally, either prior to or during reverse transcription...
Ty1 copy number dynamics in SaccharomycesDavid J Garfinkel
Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland 21701 1201, USA
Genetics 169:1845-57. 2005..Ty1 gain/loss ratios obtained under different conditions suggest that copy number oscillates over time by altering the rate of retrotransposition, resulting in the diverse copy numbers observed in Saccharomyces...
Retrotransposon suicide: formation of Ty1 circles and autointegration via a central DNA flapDavid J Garfinkel
National Cancer Institute, P O Box B, Frederick, MD 21702 1201, USA
J Virol 80:11920-34. 2006..These results suggest that Ty1-specific mechanisms minimize copy number and raise the possibility that special DNA structures are a targeting determinant...
Chromatin-associated genes protect the yeast genome from Ty1 insertional mutagenesisKatherine M Nyswaner
Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, Science Applications International Corporation, National Cancer Institute, Frederick, Maryland 21702 1201, USA
Genetics 178:197-214. 2008..Our results indicate that multiple pathways restrict Ty1 mobility and histone modifications may protect coding regions from insertional mutagenesis...
P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particlesMary Ann Checkley
Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute Frederick, P O Box B, Frederick, MD 21702 1201, USA
Mol Cell Biol 30:382-98. 2010..Therefore, Kem1p may prevent the aggregation of Ty1 antisense and mRNAs. Overall, our results suggest that P-body components enhance the formation of retrotransposition-competent Ty1 VLPs...
Posttranslational interference of Ty1 retrotransposition by antisense RNAsEmiko Matsuda
Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702 1201, USA
Proc Natl Acad Sci U S A 106:15657-62. 2009..Thus, Ty1AS RNAs are part of an intrinsic mechanism that limits retrotransposition by reducing the level of proteins required for replication and integration...
Exploring Ty1 retrotransposon RNA structure within virus-like particlesKatarzyna J Purzycka
RT Biochemistry Section, HIV Drug Resistance Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA
Nucleic Acids Res 41:463-73. 2013..Our results support the idea that antisense RNAs inhibit retrotransposition by targeting Ty1 protein function rather than annealing with the RNA genome...
BUD22 affects Ty1 retrotransposition and ribosome biogenesis in Saccharomyces cerevisiaeArun Dakshinamurthy
Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland 21702, USA
Genetics 185:1193-205. 2010..Together our results suggest that BUD22 is involved in a step in ribosome biogenesis that not only affects general translation, but also may alter the frameshifting efficiency of ribosomes, an event central to Ty1 retrotransposition...
Functional analysis of N-terminal residues of ty1 integraseSharon P Moore
Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland 21702, USA
J Virol 83:9502-11. 2009..Our results suggest that the histidine/cysteine residues are important for steps in transposition prior to integration, while the hydrophobic residues function in IN multimerization...
Ty1 gag enhances the stability and nuclear export of Ty1 mRNAMary Ann Checkley
Gene Regulation and Chromosome Biology Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA
Traffic 14:57-69. 2013..Endogenously expressed Gag also localized to the nuclear periphery independent of RNA export. These results suggest that Gag is required for Ty1 mRNA stability, efficient nuclear export and localization into cytoplasmic foci...
Sensitive phenotypic detection of minor drug-resistant human immunodeficiency virus type 1 reverse transcriptase variantsDwight V Nissley
Basic Research Program, SAIC Frederick, NCI Frederick, P O Box B, Frederick, MD 21702, USA
J Clin Microbiol 43:5696-704. 2005....
Analysis of a Ty1-less variant of Saccharomyces paradoxus: the gain and loss of Ty1 elementsSharon P Moore
Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute, PO Box B, Frederick, MD 21702 1201, USA
Yeast 21:649-60. 2004..The results indicate that Ty1 retrotransposition occurs at a much higher rate than elimination, suggesting that copy-number-dependent co-factors or environmental conditions contribute to the loss of Ty elements in this genome...
The Rad27 (Fen-1) nuclease inhibits Ty1 mobility in Saccharomyces cerevisiaeAnuradha Sundararajan
Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute, Frederick, Maryland 21702, USA
Genetics 163:55-67. 2003..Our results suggest that Rad27 inhibits Ty1 mobility by destabilizing unincorporated Ty1 cDNA and preventing the formation of Ty1 multimers...
S-phase checkpoint pathways stimulate the mobility of the retrovirus-like transposon Ty1M Joan Curcio
Laboratory of Developmental Genetics, Wadsworth Center, Albany, New York 12201, USA
Mol Cell Biol 27:8874-85. 2007..We propose that DNA lesions created in the absence of Rtt/genome caretakers trigger S-phase checkpoint pathways to stimulate Ty1 reverse transcriptase activity...
Survival strategies for transposons and genomesSandra L Martin
Department of Cellular and Structural Biology, University of Colorado School of Medicine, Box B111, 4200 E, Ninth Avenue, Denver, CO 80262, USA
Genome Biol 4:313. 2003..A report on the Keystone Symposium "Transposition and other genome rearrangements", Santa Fe, USA, 8-14 February 2003...
