Qian Chen, Huang Chaoyu, Luo Qinghui, Qin Kaili, Wu Yangyang, Liao Lin, Zhang Qian, Xiang Liqun, Yan Jie
Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, Guangxi Zhuang Autonomous Region, People's Republic of China.
Organizing Personnel Section, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region, People's Republic of China.
J Clin Lab Anal. 2024 Dec;38(24):e25123. doi: 10.1002/jcla.25123. Epub 2024 Dec 12.
Congenital hypofibrinogenemia, a quantitative fibrinogen disorder, is characterized by abnormally low levels of both functional and antigen fibrinogen. We identified a heterozygous nonsense mutation, p.Arg17Stop, in the fibrinogen Bβ chain of a three-month-old female infant.
Coagulation testing, gene analysis, in vitro plasmid construction, and functional analyses were conducted to investigate the underlying pathogenic mechanisms.
Plasma fibrinogen levels showed decrease in the proband. DNA sequencing of the proband revealed a heterozygous point mutation (c.139C>T) in exon 2 of the FGB gene causing Arg → Stop substitution. Human Arg17 was found to be highly conserved. In vitro expression analyses indicated that the mutation impacts both the transcription and translation of the FGB gene, subsequently affecting the synthesis and secretion of fibrinogen.
The p.Arg17Stop mutation in the fibrinogen Bβ chain disrupts fibrinogen production and secretion, contributing to hypofibrinogenemia.
先天性低纤维蛋白原血症是一种纤维蛋白原定量紊乱疾病,其特征是功能性和抗原性纤维蛋白原水平均异常降低。我们在一名三个月大的女婴的纤维蛋白原Bβ链中鉴定出一个杂合性无义突变,即p.Arg17Stop。
进行凝血检测、基因分析、体外质粒构建和功能分析以研究潜在的致病机制。
先证者的血浆纤维蛋白原水平降低。对先证者的DNA测序显示,FGB基因第2外显子存在一个杂合点突变(c.139C>T),导致精氨酸被替换为终止密码子。发现人类的第17位精氨酸高度保守。体外表达分析表明,该突变影响FGB基因的转录和翻译,进而影响纤维蛋白原的合成和分泌。
纤维蛋白原Bβ链中的p.Arg17Stop突变破坏了纤维蛋白原的产生和分泌,导致低纤维蛋白原血症。