Functional analysis of the transcriptional activity of the mouse phospholipid transfer protein gene

被引:29
作者
Tu, AY [1 ]
Albers, JJ [1 ]
机构
[1] Univ Washington, Dept Med, NW Lipid Res Labs, Seattle, WA 98103 USA
关键词
mouse gene; phospholipid transfer protein; transcriptional regulation;
D O I
10.1006/bbrc.2001.5687
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
Phospholipid transfer protein (PLTP) plays an important role in the metabolism of plasma high density lipoprotein. The mouse gene encoding PLTP and its promoter region has been cloned in our laboratory. The present study was conducted to functionally analyze the transcriptional regulation of the mouse PLTP gene. The results indicated that DNA sequences between -245 and -69 were responsible for the full promoter activity and binding motifs for transcription factor Sp1 and AP-2 within this functional promoter region were synergistically essential for the basal transcription. The transcriptional activity of this gene was significantly increased by chenodeoxycholic acid and fenofibrate, suggesting that transcription factor farnesoid X-activated receptor (FXR) and peroxisome proliferator-activated receptor (PPAR) are likely involved in the transcriptional regulation. DNA sequence analysis suggests that DNA sequences from -407 to -395 and from -393 to -381 are homologous to the recognition motifs of FXR, and those from -859 to -847 and from -309 to -297 are similar to the potential binding motif for PPAR. These findings provide a molecular basis for further investigation of the physiological function and regulation of the PLTP gene in mice. (C) 2001 Academic Press.
引用
收藏
页码:921 / 926
页数:6
相关论文
共 25 条
[1]   Transgenic mice expressing human phospholipid transfer protein have increased HDL non-HDL cholesterol ratio [J].
Albers, JJ ;
Tu, AY ;
Paigen, B ;
Chen, H ;
Cheung, MC ;
Marcovina, SM .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1996, 26 (04) :262-267
[2]   FUNCTIONAL EXPRESSION OF HUMAN AND MOUSE PLASMA PHOSPHOLIPID TRANSFER PROTEIN - EFFECT OF RECOMBINANT AND PLASMA PLTP ON HDL SUBSPECIES [J].
ALBERS, JJ ;
WOLFBAUER, G ;
CHEUNG, MC ;
DAY, JR ;
CHING, AFT ;
LOK, S ;
TU, AY .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1995, 1258 (01) :27-34
[3]   Induction of the phospholipid transfer protein gene accounts for the high density lipoprotein enlargement in mice treated with fenofibrate [J].
Bouly, M ;
Masson, D ;
Gross, B ;
Jiang, XC ;
Fievet, C ;
Castro, G ;
Tall, AR ;
Fruchart, JC ;
Staels, B ;
Lagrost, L ;
Luc, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (28) :25841-25847
[4]  
Ehnholm S, 1998, J LIPID RES, V39, P1248
[5]   Plasma phospholipid transfer protein - Adenovirus-mediated overexpression in mice leads to decreased plasma high density lipoprotein (HDL) and enhanced hepatic uptake of phospholipids and cholesteryl esters from HDL [J].
Foger, B ;
SantamarinaFojo, S ;
Shamburek, RD ;
Parrot, CL ;
Talley, GD ;
Brewer, HB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :27393-27400
[6]   The impact of phospholipid transfer protein (PLTP) on HDL metabolism [J].
Huuskonen, J ;
Olkkonen, VM ;
Jauhiainen, M ;
Ehnholm, C .
ATHEROSCLEROSIS, 2001, 155 (02) :269-281
[7]   Targeted mutation of plasma phospholipid transfer protein gene markedly reduces high-density lipoprotein levels [J].
Jiang, XC ;
Bruce, C ;
Mar, J ;
Lin, M ;
Ji, Y ;
Francone, OL ;
Tall, AR .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (06) :907-914
[8]   Apolipoprotein B secretion and atherosclerosis are decreased in mice with phospholipid-transfer protein deficiency [J].
Jiang, XC ;
Qin, SC ;
Qiao, CP ;
Kawano, K ;
Lin, M ;
Skold, A ;
Xiao, X ;
Tall, AR .
NATURE MEDICINE, 2001, 7 (07) :847-852
[9]   Increased pre beta-high density lipoprotein, apolipoprotein AI, and phospholipid in mice expressing the human phospholipid transfer protein and human apolipoprotein AI transgenes [J].
Jiang, XC ;
Francone, OL ;
Bruce, C ;
Milne, R ;
Mar, J ;
Walsh, A ;
Breslow, JL ;
Tall, AR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (10) :2373-2380
[10]   Identification of the DNA binding specificity and potential target genes for the farnesoid X-activated receptor [J].
Laffitte, BA ;
Kast, HR ;
Nguyen, CM ;
Zavacki, AM ;
Moore, DD ;
Edwards, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) :10638-10647