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Characterization of human Collagen XVIII promoter 2: Interaction of Sp1, Sp3 and YY1 with the regulatory region and a SNP that increases transcription in hepatocytes
被引:10
作者:
Armelin-Correa, LM
Lin, CJ
Barbosa, A
Bagatini, K
Winnischofer, SMB
Sogayar, MC
Passos-Bueno, MR
机构:
[1] Univ Sao Paulo, Biosci Inst, Dept Genet & Evolut Biol, Sao Paulo, Brazil
[2] Univ Sao Paulo, FMUSP, Hosp Clin, Dept Pathol, Sao Paulo, Brazil
[3] Univ Sao Paulo, FMUSP, Hosp Clin, Div Endocrinol, Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Chem, Dept Biochem, Sao Paulo, Brazil
基金:
巴西圣保罗研究基金会;
关键词:
Collagen XVIII;
transcriptional regulation;
functional SNP;
Sp1;
Sp3;
YY1;
D O I:
10.1016/j.matbio.2005.08.003
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:
Different levels of Collagen XVIII expression have been associated with several pathological processes such as cancer, liver fibrosis, diabetic retinopathy and Alzheimer's disease. Understanding the transcriptional regulation of Collagen XVIII might elucidate some pathways related to the progression of these diseases. The promoter 2 of COL18A1 gene is poorly understood and is responsible for the transcription of this gene in several adult tissues such as liver, eyes and brain. This study focused upon characterization of cis-regulatory elements interacting with human COL18A1 promoter 2 and identification of SNPs in this region in different ethnic groups. Our results show that there are five conserved regions (I to V) between human and mouse promoter 2 and that the human COL18A1 core promoter is located between nucleotides -186 and -21. Sp1 and Sp3 bind to conserved regions I and V, while Sp3 and YY1 interact with region II. We have verified that the SNP at position -700 (T > G) is embedded in two common haplotypes, which have different frequencies between European and African descendents. The allele -700G increases transcription and binding for a still unknown transcription factor. SNP -700 affects Sp3 and YY1 interaction with this region, even though it is not part of these transcription factors' predicted binding sites. Therefore, our results show for the first time that Sp3 and YY1 interact with human COL18A1 promoter 2, and that nucleotide -700 is part of a binding motif for a still unknown TF that is involved in the expression of this gene in hepatocytes. In addition, we also confirm the involvement of Sp1 in the regulation of this gene. (c) 2005 Elsevier B.V./International Society of Matrix Biology. All rights reserved.
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页码:550 / 559
页数:10
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