K562 cells implicate increased chromatin accessibility in Alu transcriptional activation

被引:35
作者
Li, TH
Kim, C
Rubin, CM
Schmid, CW [1 ]
机构
[1] Univ Calif Davis, Sect Mol & Cellular Biol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
关键词
D O I
10.1093/nar/28.16.3031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alu repeats in K562 cells are unusually hypomethylated and far more actively transcribed than those in other human cell lines and somatic tissues. Also, the level of Alu RNA in K562 cells is relatively insensitive to cell stresses, namely heat shock, adenovirus infection and treatment with cycloheximide, which increase the abundance of Alu RNA in HeLa and 293 cells. Recent advances in understanding the interactions between DNA methylation, transcriptional activation and chromatin conformation reveal reasons for the constitutively high level of Alu expression in K562 cells, Methylation represses transcription of transiently transfected Alu templates in all cell lines tested but cell stresses do not relieve this repression suggesting that they activate Alu transcription through another pathway, A relatively large fraction of the Alus within K562 chromatin is accessible to restriction enzyme cleavage and cell stresses increase the chromatin accessibility of Alus in HeLa and 293 cells, Cell stress evidently activates Alu transcription by rapidly remodeling chromatin to recruit additional templates.
引用
收藏
页码:3031 / 3039
页数:9
相关论文
共 59 条
[1]   TRANSCRIPTION INVIVO OF AN ALU FAMILY MEMBER UPSTREAM FROM THE HUMAN EPSILON-GLOBIN GENE [J].
ALLAN, M ;
PAUL, J .
NUCLEIC ACIDS RESEARCH, 1984, 12 (02) :1193-1200
[2]   DISPERSION AND INSERTION POLYMORPHISM IN 2 SMALL SUBFAMILIES OF RECENTLY AMPLIFIED HUMAN ALU REPEATS [J].
BATZER, MA ;
RUBIN, CM ;
HELLMANNBLUMBERG, U ;
ALEGRIAHARTMAN, M ;
LEEFLANG, EP ;
STERN, JD ;
BAZAN, HA ;
SHAIKH, TH ;
DEININGER, PL ;
SCHMID, CW .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 247 (03) :418-427
[3]  
BELLARD M, 1989, METHOD ENZYMOL, V170, P317
[4]   DNA METHYLATION INHIBITS TRANSCRIPTION BY RNA POLYMERASE-III OF A TRANSFER RNA-GENE, BUT NOT OF A 5S RIBOSOMAL-RNA-GENE [J].
BESSER, D ;
GOTZ, F ;
SCHULZEFORSTER, K ;
WAGNER, H ;
KROGER, H ;
SIMON, D .
FEBS LETTERS, 1990, 269 (02) :358-362
[5]   Gene silencing - Methylation meets acetylation [J].
Bestor, TH .
NATURE, 1998, 393 (6683) :311-312
[6]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8
[7]   GENE NUMBER, NOISE-REDUCTION AND BIOLOGICAL COMPLEXITY [J].
BIRD, AP .
TRENDS IN GENETICS, 1995, 11 (03) :94-100
[8]   SPECIFIC REGULATION OF XENOPUS CHROMOSOMAL 5S RIBOSOMAL-RNA GENE-TRANSCRIPTION IN-VIVO BY HISTONE H1 [J].
BOUVET, P ;
DIMITROV, S ;
WOLFFE, AP .
GENES & DEVELOPMENT, 1994, 8 (10) :1147-1159
[9]   INDUCTION OF SPECIFIC TRANSCRIPTION BY RNA POLYMERASE-III IN TRANSFORMED-CELLS [J].
CAREY, MF ;
SINGH, K ;
BOTCHAN, M ;
COZZARELLI, NR .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (09) :3068-3076
[10]   ENHANCED B2 TRANSCRIPTION IN SIMIAN VIRUS-40-TRANSFORMED CELLS IS MEDIATED THROUGH THE FORMATION OF RNA POLYMERASE-III TRANSCRIPTION COMPLEXES ON PREVIOUSLY INACTIVE GENES [J].
CAREY, MF ;
SINGH, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7059-7063