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* Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research and
Advanced Biomedical Computing Center, Science Applications International Corporation, National Cancer Institute, Frederick, Maryland 21702-1201
1 Corresponding author: National Cancer Institute, PO Box B, Frederick, MD 21702-1201.
E-mail: garfinke{at}ncifcrf.gov
and elf1
, suggesting that Ty1 integration may be more efficient in these strains. Insertion-site preference at the CAN1 locus requires Ty1 restriction genes involved in histone H2B ubiquitination by Paf complex subunit genes, as well as BRE1 and RAD6, histone H3 acetylation by RTT109 and ASF1, and transcription elongation by SPT5. Our results indicate that multiple pathways restrict Ty1 mobility and histone modifications may protect coding regions from insertional mutagenesis.
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