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Genetics, Vol. 172, 2157-2167, April 2006, Copyright © 2006
doi:10.1534/genetics.105.054072
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,1
* Laboratory of Developmental Genetics, Wadsworth Center, Albany, New York 12201-2002 and
Department of Biomedical Sciences, University at Albany School of Public Health, Albany, New York 12201-0509
1 Corresponding author: Center for Medical Sciences, Wadsworth Center, P.O. Box 22002, Albany, NY 12201-2002.
E-mail: curcio{at}wadsworth.org
or set3
mutants, transposition of endogenous Ty1 elements into the upstream regions of tRNAGly genes was substantially decreased. Furthermore, when equivalent numbers of Ty1HIS3 mobility events launched from a pGAL1:Ty1his3AI plasmid were analyzed, only one-quarter to one-half as many were found upstream of tRNAGly genes in a hos2
or set3
mutant than in a wild-type strain. Chromatin immunoprecipitation analysis revealed that Hos2 is physically associated with tRNA genes. Taken together, our results support the hypothesis that Hos2 and Set3 function at tRNA genes to promote Ty1 integration. This article has been cited by other articles:
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