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

被引:150
作者
Ahmed, Sara [1 ]
Brickner, Donna G. [1 ]
Light, William H. [1 ]
Cajigas, Ivelisse [1 ]
McDonough, Michele [2 ]
Froyshteter, Alexander B. [1 ]
Volpe, Tom [2 ]
Brickner, Jason H. [1 ]
机构
[1] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Evanston, IL 60208 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Cell & Mol Biol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
UNFOLDED PROTEIN RESPONSE; SACCHAROMYCES-CEREVISIAE; REVERSE RECRUITMENT; ACTIVE GENES; PORE; EXPRESSION; TRANSCRIPTION; LOCALIZATION; ORGANIZATION; ASSOCIATION;
D O I
10.1038/ncb2011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:111 / U43
页数:28
相关论文
共 40 条
[1]   3′-end formation signals modulate the association of genes with the nuclear periphery as well as mRNP dot formation [J].
Abruzzi, Katharine C. ;
Belostotsky, Dmitry A. ;
Chekanova, Julia A. ;
Dower, Ken ;
Rosbash, Michael .
EMBO JOURNAL, 2006, 25 (18) :4253-4262
[2]   Regulation and epigenetic control of transcription at the nuclear periphery [J].
Ahmed, Sara ;
Brickner, Jason H. .
TRENDS IN GENETICS, 2007, 23 (08) :396-402
[3]   The nuclear envelope and transcriptional control [J].
Akhtar, Asifa ;
Gasser, Susan M. .
NATURE REVIEWS GENETICS, 2007, 8 (07) :507-517
[4]   The molecular architecture of the nuclear pore complex [J].
Alber, Frank ;
Dokudovskaya, Svetlana ;
Veenhoff, Liesbeth M. ;
Zhang, Wenzhu ;
Kipper, Julia ;
Devos, Damien ;
Suprapto, Adisetyantari ;
Karni-Schmidt, Orit ;
Williams, Rosemary ;
Chait, Brian T. ;
Sali, Andrej ;
Rout, Michael P. .
NATURE, 2007, 450 (7170) :695-701
[5]   H2A.z-mediated localization of genes at the nuclear periphery confers epigenetic memory of previous transcriptional state [J].
Brickner, Donna Garvey ;
Cajigas, Ivelisse ;
Fondufe-Mittendorf, Yvonne ;
Ahmed, Sara ;
Lee, Pei-Chih ;
Widom, Jonathan ;
Brickner, Jason H. .
PLOS BIOLOGY, 2007, 5 (04) :704-716
[6]  
Brickner Jason H, 2004, PLoS Biol, V2, pe342
[7]   SAGA interacting factors confine sub-diffusion of transcribed genes to the nuclear envelope [J].
Cabal, Ghislain G. ;
Genovesio, Auguste ;
Rodriguez-Navarro, Susana ;
Zimmer, Christophe ;
Gadal, Olivier ;
Lesne, Annick ;
Buc, Henri ;
Feuerbach-Fournier, Frank ;
Olivo-Marin, Jean-Christophe ;
Hurt, Eduard C. ;
Nehrbass, Ulf .
NATURE, 2006, 441 (7094) :770-773
[8]   GENECODIS: a web-based tool for finding significant concurrent annotations in gene lists [J].
Carmona-Saez, Pedro ;
Chagoyen, Monica ;
Tirado, Francisco ;
Carazo, Jose M. ;
Pascual-Montano, Alberto .
GENOME BIOLOGY, 2007, 8 (01)
[9]   Developmentally induced changes in transcriptional program alter spatial organization across chromosomes [J].
Casolari, JM ;
Brown, CR ;
Drubin, DA ;
Rando, OJ ;
Silver, PA .
GENES & DEVELOPMENT, 2005, 19 (10) :1188-1198
[10]   Genome-wide localization of the nuclear transport machinery couples transcriptional status and nuclear organization [J].
Casolari, JM ;
Brown, CR ;
Komili, S ;
West, J ;
Hieronymus, H ;
Silver, PA .
CELL, 2004, 117 (04) :427-439