Tilson M D, Reilly J M, Brophy C M, Webster E L, Barnett T R
Department of Surgery, St. Luke's Roosevelt Hospital Center, New York, NY 10019.
J Vasc Surg. 1993 Aug;18(2):266-70.
The tissue inhibitors of metalloproteinases (TIMPs) are major inhibitors of several enzymes that are destructive to connective tissue, and TIMP-1 has been reported to be deficient in the wall of abdominal aortic aneurysms. This deficiency could represent failure of expression resulting from either local tissue conditions or mutation in the primary structure of the gene (or one of its regulatory elements).
Southern blotting techniques were used to examine the possibility of global deletions or inserts in the gene (14 patients); Northern blot techniques were performed to examine the expression of the mRNAs in cultured fibroblasts under basal conditions (six patients); and sequence analysis of the cDNA derived from fibroblast mRNAs was done after amplification by polymerase chain reaction (six patients).
The Southern blots revealed a normal distribution of the known alleles of the gene without unique restriction-length polymorphisms. Fibroblast expression of TIMP mRNA was normal under basal conditions. Sequence analysis of the cDNAs revealed an identical-point polymorphism in two of the six patients (a single base pair substitution of C-->T at the third position in codon 101), but the amino acid was conserved.
The studies reported here do not support the hypothesis that deficiency of TIMP-1 in specimens of aorta of patients with abdominal aortic aneurysms results from a primary genetic defect.
金属蛋白酶组织抑制剂(TIMPs)是几种对结缔组织有破坏作用的酶的主要抑制剂,据报道,腹主动脉瘤壁中TIMP - 1缺乏。这种缺乏可能是由于局部组织条件或基因一级结构(或其调控元件之一)的突变导致的表达失败。
采用Southern印迹技术检测基因中整体缺失或插入的可能性(14例患者);采用Northern印迹技术检测基础条件下培养的成纤维细胞中mRNA的表达(6例患者);通过聚合酶链反应扩增后,对成纤维细胞mRNA衍生的cDNA进行序列分析(6例患者)。
Southern印迹显示该基因已知等位基因分布正常,无独特的限制性片段长度多态性。基础条件下成纤维细胞TIMP mRNA表达正常。cDNA序列分析显示,6例患者中有2例存在同一位点多态性(密码子101第三位的单个碱基对由C突变为T),但氨基酸保守。
本研究报告不支持腹主动脉瘤患者主动脉标本中TIMP - 1缺乏是由原发性基因缺陷导致的假说。