High-mobility group-I/Y proteins: Potential role in the pathophysiology of critical illnesses

被引:17
作者
Carvajal, IM
Baron, RM
Perrella, MA
机构
[1] Brigham & Womens Hosp, Div Pulm & Crit Care, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
关键词
high-mobility group proteins; transcriptional regulation; nuclear protein-DNA complex; enhanceosome; inflammation; sepsis;
D O I
10.1097/00003246-200201001-00005
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
High-mobility group (HMG) proteins are architectural factors that have been shown to play a role in the transcriptional regulation of various mammalian genes. One family of HMG proteins, HMG-I/Y, is known to facilitate the initiation of gene transcription by modifying the conformation of DNA and recruiting transcription factors into an organized complex on transcriptional regulatory regions of specific genes. In many circumstances, the nuclear factor-kappaB family of transcription factors is involved in gene regulation that is mediated by HIVIG-I/Y. We will review the mechanisms by which HMG-I/Y proteins regulate gene transcription, give an overview of selected genes regulated by HMG-I/Y, summarize the potential roles of these genes in critical illnesses, and provide more detailed information about the role of HMG-I/Y in the regulation of nitric oxide synthase-2 during an inflammatory response, such as endotoxemia/sepsis.
引用
收藏
页码:S36 / S42
页数:7
相关论文
共 86 条
[31]   Hypoxia induces high-mobility-group protein I(Y) and transcription of the cyclooxygenase-2 gene in human vascular endothelium [J].
Ji, YS ;
Xu, Q ;
Schmedtje, JF .
CIRCULATION RESEARCH, 1998, 83 (03) :295-304
[32]  
JOHNSON KR, 1988, J BIOL CHEM, V263, P18338
[33]   THE NONHISTONE CHROMOSOMAL PROTEIN HMG-I(Y) CONTRIBUTES TO REPRESSION OF THE IMMUNOGLOBULIN HEAVY-CHAIN GERM-LINE EPSILON-RNA PROMOTER [J].
KIM, J ;
REEVES, R ;
ROTHMAN, P ;
BOOTHBY, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (03) :798-808
[34]   The mechanism of transcriptional synergy of an in vitro assembled interferon-β enhanceosome [J].
Kim, TK ;
Maniatis, T .
MOLECULAR CELL, 1997, 1 (01) :119-129
[35]  
Kirkeboen KA, 1999, ACTA ANAESTH SCAND, V43, P275
[36]   HMG I(Y) interferes with the DNA binding of NF-AT factors and the induction of the interleukin 4 promoter in T cells [J].
KleinHessling, S ;
Schneider, G ;
Heinfling, A ;
Chuvpilo, S ;
Serfling, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) :15311-15316
[37]   COOPERATIVITY BETWEEN 2 NF-KAPPA-B COMPLEXES, MEDIATED BY HIGH-MOBILITY-GROUP PROTEIN-I(Y), IS ESSENTIAL FOR CYTOKINE-INDUCED EXPRESSION OF THE E-SELECTIN PROMOTER [J].
LEWIS, H ;
KASZUBSKA, W ;
DELAMARTER, JF ;
WHELAN, J .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :5701-5709
[38]   MACROPHAGE NITRIC-OXIDE SYNTHASE GENE - 2 UPSTREAM REGIONS MEDIATE INDUCTION BY INTERFERON-GAMMA AND LIPOPOLYSACCHARIDE [J].
LOWENSTEIN, CJ ;
ALLEY, EW ;
RAVAL, P ;
SNOWMAN, AM ;
SNYDER, SH ;
RUSSELL, SW ;
MURPHY, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (20) :9730-9734
[39]   ALTERED RESPONSES TO BACTERIAL-INFECTION AND ENDOTOXIC-SHOCK IN MICE LACKING INDUCIBLE NITRIC-OXIDE SYNTHASE [J].
MACMICKING, JD ;
NATHAN, C ;
HOM, G ;
CHARTRAIN, N ;
FLETCHER, DS ;
TRUMBAUER, M ;
STEVENS, K ;
XIE, QW ;
SOKOL, K ;
HUTCHINSON, N ;
CHEN, H ;
MUDGETT, JS .
CELL, 1995, 81 (04) :641-650
[40]   Acetylation of HMG I(Y) by CBP turns off IFNβ expression by disrupting the enhanceosome [J].
Munshi, N ;
Merika, M ;
Yie, JM ;
Senger, K ;
Chen, GY ;
Thanos, D .
MOLECULAR CELL, 1998, 2 (04) :457-467