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Chromatin and DNA methylation dynamics of Helicobacter pylori-induced COX-2 activation
被引:33
|作者:
Pero, Raffaela
[2
,3
]
Peluso, Silvia
[2
,3
]
Angrisano, Tiziana
[2
,3
]
Tuccillo, Concetta
[2
,3
]
Sacchetti, Silvana
[2
,3
,4
]
Keller, Simona
[2
,3
]
Tomaiuolo, Rossella
[4
]
Bruni, Carmelo B.
[2
,3
]
Lembo, Francesca
[1
]
Chiariotti, Lorenzo
[1
,2
,3
]
机构:
[1] Univ Naples Federico II, Fac Farm, Dipartimento Chim Farmaceut & Tossicol, I-80131 Naples, Italy
[2] Fac Farm, Naples, Italy
[3] Fac Sci Biotecnol, Dipartimento Biol & Patol Cellulare & Mol L Calif, Naples, Italy
[4] CEINGE Biotecnol Avanzate, Dipartimento Biochim & Biotecnol Med, Naples, Italy
关键词:
Helicobacter pylori;
Chromatin modifications;
DNA methylation;
COX-2;
Gastric cells;
GASTRIC EPITHELIAL-CELLS;
INCREASED EXPRESSION;
CLINICAL-RELEVANCE;
INFECTION;
PROMOTER;
PROTEIN;
CANCER;
GENES;
D O I:
10.1016/j.ijmm.2010.06.009
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
COX-2 expression is altered in gastrointestinal diseases. Helicobacter pylori (Hp) infection may have a critical role in COX-2 disregulation. We undertook this study to investigate possible chromatin and DNA methylation changes occurring early during COX-2 gene activation as a direct consequence of Hp-gastric cells interaction. We show that Hp infection is followed by different expression, chromatin and DNA methylation changes including: (i) biphasic activation of COX-2 gene; (ii) rapid remodulation of HDACs expression and activity, increased acetylation and release of HDAC from COX-2 promoter; (iii) transient gradual increase of H3 acetylation and H3K4 dimethylation and decrease of H3K9 dimethylation; (iv) late and long-lasting increase of H3K27 trimethylation; (v) rapid cyclical DNA methylation/demethylation events at 8 specific CpG sites (-176, -136, +25, +36, +57, +82, +198, +231) surrounding the COX-2 gene transcriptional start site. Our data indicate that specific chromatin and DNA methylation changes occur at COX-2 gene in the first phases of Hp exposure in cultured gastric cells as a primary response to host-parasite interaction. (C) 2010 Elsevier GmbH. All rights reserved.
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页码:140 / 149
页数:10
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