Identification of negative and positive regulatory elements in the rat alpha 1(I) collagen gene promoter

被引:7
作者
Dhalla, AK
Kandala, JC
Weber, KT
Guntaka, RV
机构
[1] UNIV MISSOURI,SCH MED,DEPT INTERNAL MED,DIV CARDIOL,COLUMBIA,MO 65212
[2] UNIV MISSOURI,SCH MED,DEPT MOL MICROBIOL & IMMUNOL,COLUMBIA,MO 65212
基金
英国医学研究理事会;
关键词
alpha 1(I)collagen gene; promoter; gene regulation; transcription;
D O I
10.1016/S1357-2725(96)00126-4
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
Type I collagen is the main constituent of extracellular matrix found in various organs including the heart. Under some pathological conditions accumulation of excess type I collagen in the interstitium leads to organ dysfunction. In order to identify the regulatory elements in the rat alpha 1(I) collagen gene promoter, deletions were made in the promoter region. Various plasmid constructs were transfected into different fibroblasts using LipofectAMINE. The results indicated a negative cis-element between nucleotides -310 to -440 in the rat alpha 1(I) collagen gene promoter. Presence of this sequence significantly diminished the reporter gene activity. In addition we have observed that the sequence between -220 to -330 contained a positively acting cis-element, which is highly active in rat fibroblasts. Analysis of the nuclear factors binding to the negative element by electrophoretic mobility shift assays indicated that similar or identical factors are present in different fibroblasts as well as human HeLa cells and that these factors appear to bind to a composite sequence within -325 to -400. Competition with different oligonucleotides suggested that two distinct but contiguous sequence motifs may constitute the negative regulatory element. Our results with the rat alpha 1(I) collagen promoter confirm the presence of a negative cis-element previously described for the mouse promoter and provided additional information on the bipartite nature of this element. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:143 / 151
页数:9
相关论文
共 24 条
[1]   REGULATION OF COLLAGEN GENE-EXPRESSION IN CUTANEOUS DISEASES WITH DERMAL FIBROSIS - EVIDENCE FOR PRETRANSLATIONAL CONTROL [J].
ABERGEL, RP ;
CHU, ML ;
BAUER, EA ;
UITTO, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1987, 88 (06) :727-731
[2]   ANALYSIS OF THE COLLAGEN ALPHA-1(I) PROMOTER [J].
BRENNER, DA ;
RIPPE, RA ;
VELOZ, L .
NUCLEIC ACIDS RESEARCH, 1989, 17 (15) :6055-6064
[3]   TYPE-I COLLAGEN GENE-REGULATION AND THE MOLECULAR PATHOGENESIS OF CIRRHOSIS [J].
BRENNER, DA ;
WESTWICK, J ;
BREINDL, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (04) :G589-G595
[4]  
BRENNER DA, 1994, J LAB CLIN MED, V124, P755
[5]   COLLAGEN-METABOLISM IN CULTURED ADULT-RAT CARDIAC FIBROBLASTS - RESPONSE TO ANGIOTENSIN-II AND ALDOSTERONE [J].
BRILLA, CG ;
ZHOU, GP ;
MATSUBARA, L ;
WEBER, KT .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (07) :809-820
[6]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[7]   RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051
[8]  
GUNTAKA RV, 1995, WOUND HEALING CARDIO, P281
[9]  
KARSENTY G, 1990, J BIOL CHEM, V265, P9934
[10]   DEVELOPMENTAL AND TISSUE-SPECIFIC EXPRESSION DIRECTED BY THE ALPHA-2 TYPE-I COLLAGEN PROMOTER IN TRANSGENIC MICE [J].
KHILLAN, JS ;
SCHMIDT, A ;
OVERBEEK, PA ;
DECROMBRUGGHE, B ;
WESTPHAL, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (03) :725-729