Levavasseur F, Liétard J, Ogawa K, Théret N, Burbelo P D, Yamada Y, Guillouzo A, Clément B
Institut National de la Santé et de la Recherche Médicale, Unité de Recherches Hépatologiques U-49, CHRU Pontchaillou, Rennes, France.
Biochem J. 1996 Feb 1;313 ( Pt 3)(Pt 3):745-52. doi: 10.1042/bj3130745.
Laminin gamma 1 chain is present in all basement membranes and is expressed at high levels in various diseases, such as hepatic fibrosis. We have identified cis- and trans-acting elements involved in the regulation of this gene in normal rat liver, as well as in hepatocyte primary cultures and hepatoma cell lines. Northern-blot analyses showed that laminin gamma 1 mRNA was barely detectable in freshly isolated hepatocytes and expressed at high levels in hepatocyte primary cultures, as early as 4 h after liver dissociation. Actinomycin D and cycloheximide treatment in vivo and in vitro indicated that laminin gamma 1 overexpression in cultured hepatocytes was under the control of transcriptional mechanisms. Transfection of deletion mutants of the 5' flanking region of murine LAMC1 gene in hepatoma cells that constitutively express laminin gamma 1 indicated that regulatory elements were located between -594 bp and -94 bp. This segment included GC- and CTC-containing motifs. Gel-shift analyses showed that two complexes were resolved with different affinity for the CTC sequence depending on the location of the GC box. The pattern of complex formation with nuclear factors from freshly isolated and cultured hepatocytes was different from that obtained with total liver and similar to that with hepatoma cells. Southwestern analysis indicated that several polypeptides bound the CTC-rich sequence. Affinity chromatography demonstrated that A M(r) 60,000 polypeptide was a major protein binding to the CTC motif. This polypeptide is probably involved in the transcriptional activation of various proto-oncogenes and extracellular matrix genes that are expressed at high levels in both hepatoma cells and early hepatocyte cultures.
层粘连蛋白γ1链存在于所有基底膜中,并且在各种疾病(如肝纤维化)中高水平表达。我们已经在正常大鼠肝脏、肝细胞原代培养物和肝癌细胞系中鉴定出参与该基因调控的顺式和反式作用元件。Northern印迹分析表明,在新鲜分离的肝细胞中层粘连蛋白γ1 mRNA几乎检测不到,而在肝细胞原代培养物中,早在肝脏解离后4小时就高水平表达。体内和体外的放线菌素D和环己酰亚胺处理表明,培养的肝细胞中层粘连蛋白γ1的过表达受转录机制的控制。将小鼠LAMC1基因5'侧翼区缺失突变体转染到组成性表达层粘连蛋白γ1的肝癌细胞中,表明调控元件位于-594 bp和-94 bp之间。该片段包含含GC和含CTC的基序。凝胶迁移分析表明,根据GC框的位置,两种复合物对CTC序列具有不同的亲和力。新鲜分离的和培养的肝细胞中核因子形成复合物的模式与全肝不同,与肝癌细胞相似。蛋白质印迹分析表明,几种多肽与富含CTC的序列结合。亲和层析表明,一种分子量为60,000的多肽是与CTC基序结合的主要蛋白质。这种多肽可能参与了在肝癌细胞和早期肝细胞培养物中高水平表达的各种原癌基因和细胞外基质基因的转录激活。