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
[51]  
PERRELLA MA, 1994, J BIOL CHEM, V269, P14595
[52]   Suppression of interleukin-1 beta-induced nitric-oxide synthase promoter/enhancer activity by transforming growth factor-beta 1 in vascular smooth muscle cells - Evidence for mechanisms other than NF-kappa B [J].
Perrella, MA ;
Patterson, C ;
Tan, L ;
Yet, SF ;
Hsieh, CM ;
Yoshizumi, M ;
Lee, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (23) :13776-13780
[53]   Arrest of endotoxin-induced hypotension by transforming growth factor beta 1 [J].
Perrella, MA ;
Hsieh, CM ;
Lee, WS ;
Shieh, S ;
Tsai, JC ;
Patterson, C ;
Lowenstein, CJ ;
Long, NC ;
Haber, E ;
Shore, S ;
Lee, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (05) :2054-2059
[54]   High mobility group-I(Y) protein facilitates nuclear factor-κB binding and transactivation of the inducible nitric-oxide synthase promoter/enhancer [J].
Perrella, MA ;
Pellacani, A ;
Wiesel, P ;
Chin, MT ;
Foster, LC ;
Ibanez, M ;
Hsieh, CM ;
Reeves, R ;
Yet, SF ;
Lee, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :9045-9052
[55]   INTERLEUKIN-2-INDUCED LUNG INJURY - THE ROLE OF COMPLEMENT [J].
RABINOVICI, R ;
SOFRONSKI, MD ;
BORBOROGLU, P ;
SPIRIG, AM ;
HILLEGAS, LM ;
LEVINE, J ;
VERNICK, J ;
SCESNEY, SM ;
FEUERSTEIN, N ;
FEUERSTEIN, G .
CIRCULATION RESEARCH, 1994, 74 (02) :329-335
[56]  
REDINI F, 1993, ARTHRITIS RHEUM, V36, P44
[57]   HMGI/Y proteins: flexible regulators of transcription and chromatin structure [J].
Reeves, R ;
Beckerbauer, L .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2001, 1519 (1-2) :13-29
[58]   Binding of HMG-I(Y) imparts architectural specificity to a positioned nucleosome on the promoter of the human interleukin-2 receptor α gene [J].
Reeves, R ;
Leonard, WJ ;
Nissen, MS .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (13) :4666-4679
[59]  
REEVES R, 1990, J BIOL CHEM, V265, P8573
[60]   PHOSPHORYLATION OF THE DNA-BINDING DOMAIN OF NONHISTONE HIGH-MOBILITY GROUP-I PROTEIN BY CDC2 KINASE - REDUCTION OF BINDING-AFFINITY [J].
REEVES, R ;
LANGAN, TA ;
NISSEN, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1671-1675