Time course gene expression in the one-carbon metabolism network using HepG2 cell line grown in folate-deficient medium

被引:17
作者
Chango, Abalo [1 ,2 ]
Nour, Afif Abdel [1 ]
Bousserouel, Souad [1 ]
Eveillard, Damien [3 ]
Anton, Pauline M. [1 ]
Gueant, Jean-Louis [2 ]
机构
[1] EGEAL, Inst Polytech LaSalle, F-60026 Beauvais, France
[2] INSERM, U724, F-54505 Vandoeuvre Les Nancy, France
[3] Univ Nantes, LINA, F-44322 Nantes, France
关键词
Folate; Gene expression; One-carbon metabolism; Nutrigenomics; METHIONINE SYNTHASE REDUCTASE; CPG ISLAND; COLORECTAL NEOPLASIA; THYMIDYLATE SYNTHASE; TRANSCRIPTION FACTOR; DNA METHYLATION; DIETARY-INTAKE; BREAST-CANCER; FOLIC-ACID; LIVER;
D O I
10.1016/j.jnutbio.2008.04.004
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 integrated view of the expression of genes involved in folate-dependent one-carbon metabolism (FOCM) under folate deficiency remains unknown. Dynamics of changes in the transcriptional expression of 28 genes involved in the FOCM network were evaluated at different time points (0, 2, 4, 6, 12, 24 and 48 h) in human hepatoma HepG2 cell line. Combined experimental and computational approaches were conducted for emphasizing characteristic patterns in the gene expression changes produced by cellular folate deficiency. Bivariate analysis showed that folate deficiency (0.3 nmol/L of folate vs. 2.27 mu mol/L in control medium) displayed rapid and coordinated regulation during the first 2 h with differential expression for hRfc1 (increased by 69%) and Ahcy (decreased by 437%). Density analysis through the time points gave evidence of differential expression for five genes (Ahcy, Cth, Gnmt, Mat1A, Mtrr and hRfc1). Differential expression of Ahcy, Gnmt, Mat1A and Mtrr was confirmed by time-series analysis gene expression. We also found a marked differential expression of Mtrr. Qualitative analysis of genes allowed identifying four clusters of gene that was coexpressed. Two of these clusters were consistent with specific metabolic functions as they associated genes involved in the remethylation (Mthfr and Mtrr) and in the transmethylation (Dnmt1 and Dnmt3B) pathways. The study shows a strong influence of folate status on Mtrr transcription in HepG2 cells. It suggests also that folate deficiency produces transcription changes that particularly involve the clusters of genes related with the remethylation and the transmethylation pathways. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:312 / 320
页数:9
相关论文
共 38 条
[1]   The impact of chromatin in human cancer: linking DNA methylation to gene silencing [J].
Ballestar, E ;
Esteller, M .
CARCINOGENESIS, 2002, 23 (07) :1103-1109
[2]  
Baylin Stephen B, 2004, Novartis Found Symp, V259, P226
[3]   ORAL FOLIC-ACID SUPPLEMENTATION FOR CERVICAL DYSPLASIA - A CLINICAL INTERVENTION TRIAL [J].
BUTTERWORTH, CE ;
HATCH, KD ;
SOONG, SJ ;
COLE, P ;
TAMURA, T ;
SAUBERLICH, HE ;
BORST, M ;
MACALUSO, M ;
BAKER, V .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 166 (03) :803-809
[4]  
Calvert Alan Hilary, 2004, Oncology (Williston Park), V18, P13
[5]   Folate status: Effects on pathways of colorectal carcinogenesis [J].
Choi, SW ;
Mason, JB .
JOURNAL OF NUTRITION, 2002, 132 (08) :2413S-2418S
[6]   CpG island methylation and expression of tumour-associated genes in lung carcinoma [J].
Dammann, R ;
Strunnikova, M ;
Schagdarsurengin, U ;
Rastetter, M ;
Papritz, M ;
Hattenhorst, UE ;
Hofmann, HS ;
Silber, RE ;
Burdach, S ;
Hansen, G .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (08) :1223-1236
[7]   Methyltransferase recruitment and DNA hypermethylation of target promoters by an oncogenic transcription factor [J].
Di Croce, L ;
Raker, VA ;
Corsaro, M ;
Fazi, F ;
Fanelli, M ;
Faretta, M ;
Fuks, F ;
Lo Coco, F ;
Kouzarides, T ;
Nervi, C ;
Minucci, S ;
Pelicci, PG .
SCIENCE, 2002, 295 (5557) :1079-1082
[8]   Folate, DNA stability and colo-rectal neoplasia [J].
Duthie, SJ ;
Narayanan, S ;
Sharp, L ;
Little, J ;
Basten, G ;
Powers, H .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2004, 63 (04) :571-578
[9]   Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductase [J].
Elmore, C. Lee ;
Wu, Xuchu ;
Leclerc, Daniel ;
Watson, Erica D. ;
Bottiglieri, Teodoro ;
Krupenko, Natalia I. ;
Krupenko, Sergey A. ;
Cross, James C. ;
Rozen, Rima ;
Gravel, Roy A. ;
Matthews, Rowena G. .
MOLECULAR GENETICS AND METABOLISM, 2007, 91 (01) :85-97
[10]   Polymorphisms in the MTHFR gene are associated with breast cancer [J].
Ergul, E ;
Sazci, A ;
Utkan, Z ;
Canturk, NZ .
TUMOR BIOLOGY, 2003, 24 (06) :286-290