James H L, Kim D J, Zheng D Q, Girolami A
Department of Biochemistry, University of Texas Health Center at Tyler 75710.
Blood Coagul Fibrinolysis. 1994 Oct;5(5):841-4. doi: 10.1097/00001721-199410000-00025.
An individual and an affected brother previously identified as having the variant prothrombin Padua I were studied in order to identify underlying genetic defects. A heterozygous mutation in the prothrombin gene exon 8 was identified as substitution of A for G at nucleotide position 7,312 (Arg271 (CGT) to His (CAT)). An abolished RsaI restriction site was used to confirm heterozygosity for the defect. Lack of the requisite cleavage of the His271-Thr272 bond in prothrombin Padua I could prevent release of fragment 2 and block the conversion of the intermediate meizothrombin des fragment 1 to alpha-thrombin, providing an explanation of reduced potential for clotting activity and for the observed mild bleeding tendency.
为了确定潜在的基因缺陷,对一名个体及其先前被鉴定为具有凝血酶原帕多瓦I变体的患病兄弟进行了研究。在凝血酶原基因外显子8中鉴定出一个杂合突变,即核苷酸位置7312处的A被G取代(Arg271(CGT)变为His(CAT))。利用一个被消除的RsaI限制性酶切位点来确认该缺陷的杂合性。凝血酶原帕多瓦I中His271-Thr272键缺乏必要的裂解可能会阻止片段2的释放,并阻断中间产物去片段1的中凝血酶向α-凝血酶的转化,这为凝血活性降低和观察到的轻度出血倾向提供了解释。