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DNA zip codes control an ancient mechanism for gene targeting to the nuclear periphery.


ABSTRACT: Many genes in Saccharomyces cerevisiae are recruited to the nuclear periphery after transcriptional activation. We have identified two gene recruitment sequences (GRS I and II) from the promoter of the INO1 gene that target the gene to the nuclear periphery. These GRSs function as DNA zip codes and are sufficient to target a nucleoplasmic locus to the nuclear periphery. Targeting requires components of the nuclear pore complex (NPC) and a GRS is sufficient to confer a physical interaction with the NPC. GRS I elements are enriched in promoters of genes that interact with the NPC, and genes that are induced by protein folding stress. Full transcriptional activation of INO1 and another GRS-containing gene requires GRS-mediated targeting of the promoter to the nuclear periphery. Finally, GRS I also functions as a DNA zip code in Schizosaccharomyces pombe, suggesting that this mechanism of targeting to the nuclear periphery has been conserved over approximately one billion years of evolution.

SUBMITTER: Ahmed S 

PROVIDER: S-EPMC2835469 | biostudies-literature | 2010 Feb

REPOSITORIES: biostudies-literature

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DNA zip codes control an ancient mechanism for gene targeting to the nuclear periphery.

Ahmed Sara S   Brickner Donna G DG   Light William H WH   Cajigas Ivelisse I   McDonough Michele M   Froyshteter Alexander B AB   Volpe Tom T   Brickner Jason H JH  

Nature cell biology 20100124 2


Many genes in Saccharomyces cerevisiae are recruited to the nuclear periphery after transcriptional activation. We have identified two gene recruitment sequences (GRS I and II) from the promoter of the INO1 gene that target the gene to the nuclear periphery. These GRSs function as DNA zip codes and are sufficient to target a nucleoplasmic locus to the nuclear periphery. Targeting requires components of the nuclear pore complex (NPC) and a GRS is sufficient to confer a physical interaction with t  ...[more]

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