The promyelocytic leukemia nuclear body: sites of activity?

被引:51
作者
Eskiw, CH [1 ]
Bazett-Jones, DP [1 ]
机构
[1] Hosp Sick Children, Cell Biol Program, Toronto, ON M5G 1X8, Canada
关键词
promyelocytic leukemia; nucleus; transcription; nuclear bodies;
D O I
10.1139/O02-079
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
The promyelocytic leukemia (PML) nuclear body is one of many subnuclear domains in the eukaryotic cell nucleus. It has received much attention in the past few years because it accumulates the promyelocytic leukemia protein called PML. This protein is implicated in many nuclear events and is found as a fusion with the retinoic acid receptor RARalpha in leukemic cells. The importance of PML bodies in cell differentiation and growth is implicated in acute promyelocitic leukemia cells, which do not contain PML bodies. Treatment of patients with drugs that reverse the disease phenotype also causes PML bodies to reform. In this review, we discuss the structure, composition, and dynamics that may provide insights into the function of PML bodies. We also discuss the repsonse of PML bodies to cellular stresses, such as virus infection and heat shock. We interpret the changes that occur as evidence for a role of these structures in gene transcription. We also examine the role of the posttranslational modification, SUMO-1 addition, in directing proteins to this nuclear body. Characterization of the mobility of PML body associated proteins further supports a role in specific nuclear events, rather than the bodies resulting from random accumulations of proteins.
引用
收藏
页码:301 / 310
页数:10
相关论文
共 125 条
[11]   The transcription coactivator CBP is a dynamic component of the promyelocytic leukemia nuclear body [J].
Boisvert, FM ;
Kruhlak, MJ ;
Box, AK ;
Hendzel, MJ ;
Bazett-Jones, DP .
JOURNAL OF CELL BIOLOGY, 2001, 152 (05) :1099-1106
[12]   An arenavirus RING (zinc-binding) protein binds the oncoprotein promyelocyte leukemia protein (PML) and relocates PML nuclear bodies to the cytoplasm [J].
Borden, KLB ;
Dwyer, EJC ;
Salvato, MS .
JOURNAL OF VIROLOGY, 1998, 72 (01) :758-766
[13]   In vivo and in vitro characterization of the B1 and B2 zinc-binding domains from the acute promyelocytic leukemia protooncoprotein PML [J].
Borden, KLB ;
Lally, JM ;
Martin, SR ;
OReilly, NJ ;
Solomon, E ;
Freemont, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1601-1606
[14]   THE SOLUTION STRUCTURE OF THE RING FINGER DOMAIN FROM THE ACUTE PROMYELOCYTIC LEUKEMIA PROTO-ONCOPROTEIN PML [J].
BORDEN, KLB ;
BODDY, MN ;
LALLY, J ;
OREILLY, NJ ;
MARTIN, S ;
HOWE, K ;
SOLOMON, E ;
FREEMONT, PS .
EMBO JOURNAL, 1995, 14 (07) :1532-1541
[15]   Two RING finger proteins, the oncoprotein PML and the arenavirus Z protein, colocalize with the nuclear fraction of the ribosomal P proteins [J].
Borden, KLB ;
Campbelldwyer, EJ ;
Carlile, GW ;
Djavani, M ;
Salvato, MS .
JOURNAL OF VIROLOGY, 1998, 72 (05) :3819-3826
[16]   NUCLEAR-BODIES (NBS) - A NEWLY REDISCOVERED ORGANELLE [J].
BRASCH, K ;
OCHS, RL .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (02) :211-223
[17]   Interactions of herpes simplex virus type 1 with ND10 and recruitment of PML to replication compartments [J].
Burkham, J ;
Coen, DM ;
Hwang, CBC ;
Weller, SK .
JOURNAL OF VIROLOGY, 2001, 75 (05) :2353-2367
[18]   TARGETING OF ADENOVIRUS E1A AND E4-ORF3 PROTEINS TO NUCLEAR MATRIX-ASSOCIATED PML BODIES [J].
CARVALHO, T ;
SEELER, JS ;
OHMAN, K ;
JORDAN, P ;
PETTERSSON, U ;
AKUSJARVI, G ;
CARMOFONSECA, M ;
DEJEAN, A .
JOURNAL OF CELL BIOLOGY, 1995, 131 (01) :45-56
[19]   Role of CBP/P300 in nuclear receptor signalling [J].
Chakravarti, D ;
LaMorte, VJ ;
Nelson, MC ;
Nakajima, T ;
Schulman, IG ;
Juguilon, H ;
Montminy, M ;
Evans, RM .
NATURE, 1996, 383 (6595) :99-103
[20]   THE PML GENE ENCODES A PHOSPHOPROTEIN ASSOCIATED WITH THE NUCLEAR MATRIX [J].
CHANG, KS ;
FAN, YH ;
ANDREEFF, M ;
LIU, JX ;
MU, ZM .
BLOOD, 1995, 85 (12) :3646-3653