期刊文献+

F9基因Arg327Ile新突变导致血友病B的分子发病机制研究 被引量:1

Studies on the molecular mechanism of haemophilia B caused by the Arg327Ile novel mutation in F9 gene
下载PDF
导出
摘要 目的探讨F9基因Arg327Ile(R327I)突变导致血友病B的分子发病机制研究。方法对1名血友病B患者作实验室和基因诊断,定点突变法构建F9基因R327I突变的表达质粒;瞬时转染HEK293细胞,一期法检测细胞上清液中凝血因子Ⅸ活性(FⅨ∶C),ELISA法检测细胞上清液和裂解中FⅨ抗原(FⅨ∶Ag),Western blotting检测R327I突变蛋白的分子量及表达量;免疫荧光共定位染色法检测突变蛋白在内质网和高尔基体内分布。结果瞬时表达显示该患者突变细胞标本上清液中R327I突变型FⅨ∶C为野生型的4.49%,明显降低;细胞上清液和裂解液FⅨ∶Ag分别为野生型的31%和129%,为交叉反应物质减低型(CRMR)。Western blotting显示细胞上清液中R327I突变蛋白分子量与野生型相同,但含量比野生型明显降低;免疫荧光共定位染色显示R327I突变蛋白在内质网中分布较野生型多,而在高尔基体中较野生型少。结论 F9基因R327I突变影响蛋白质合成和分泌,突变蛋白较野生型表达量偏低,同时R327I突变蛋白存在凝血功能缺陷从而导致血友病B。 Objective To investigate the molecular mechanism of haemophilia B caused by a novel mutation of Arg327Ile(R327I) in F9 gene.Methods Laboratory and genetic analysis were performed in a haemophilia B patient.The R327I mutation expression plasmid was constructed with site-directed mutagenesis method based on the wild-type(WT) FⅨ expression plasmid.After the HEK293 cell was transiently transfected,the activity of FⅨ(FⅨ:C) was assayed by one stage method in the conditioned medium,while the FⅨ:Ag was measured by ELISA in both the conditioned media and the cell lysates.The molecular weight and the quantity of expressed FⅨ were analyzed by Western blot.Immunofluorescence co-localization analysis was used to examine the synthesis and secretion of the mutant protein.Results FⅨ:C of the R327I mutant protein was 4.49% of the WT in the conditioned medium,and the FⅨ:Ag of the R327I mutant protein in the conditioned medium and the cell lysates was 31% and 129% respectively,compared to the WT.The mutation was characterized as cross-reaction material reduced(CRMR).Western blot analysis showed that the molecular weight of R327I protein was the same as the WT,but the amount was much less compared with WT in the conditioned medium.Immunofluorescence co-localization assays showed that there was much R327I protein in ER and less in Golgi compared with WT,implying abnormal secretion from ER to Golgi.Conclusion The abnormal synthesis and secretion as well as the abnormal function of the R327I mutant protein caused haemophilia B.
出处 《中国输血杂志》 CAS CSCD 北大核心 2011年第5期372-376,共5页 Chinese Journal of Blood Transfusion
基金 国家自然科学基金面上项目(30770904) 上海市教委科研创新项目(07zz39)
关键词 血友病B 凝血因子Ⅸ F9基因 基因突变 发病机制 Haemophilia B Coagulation factor Ⅸ F9 gene Gene mutation Pathogenesy
  • 相关文献

参考文献11

  • 1Amy E. Schmidt and S. Paul Bajaj. Structure Function Relation- ships in Factor IX and Factor IX a. Trends Cardinvasc Meal,2003, 13( 1 ) :3945. 被引量:1
  • 2Chen SH, Yoshitake S,Chance PF, et al. An intragenic deletion of the iactor IX gene in a tamily with hemophilia B. J Clin Invest, 1985,76:2161-2164. 被引量:1
  • 3戴菁,刘湘帆,王学锋,傅启华,王文斌,丁秋兰,王鸿利.中国汉族血友病B家系五种新的FⅨ基因突变的研究[J].中华检验医学杂志,2005,28(11):1117-1119. 被引量:10
  • 4戴菁,丁秋兰,王学锋,王鸿利.两种新突变导致血友病B的分子发病机制研究[J].中华检验医学杂志,2010,33(9):878-883. 被引量:4
  • 5Ljung R,Petrini P,Tengborn L, et al. Haemophilia B mutations in Sweden :a population-based study of mutational heterogeneity. Brit J Haemat. 2001,113 ( 1 ) : 81-86. 被引量:1
  • 6Lin SW,Shen MC. Genetic basis and carrier detection of hemophil-ia B of Chinese origin. Thromb Haemost, 1993,69 (3) :247-252. 被引量:1
  • 7Bottema CD, Ketterling RP, Ii S, et al. Missense mutations and evo- lutionary conservation of amino acids:evidence that many of the a- mino acids in factor IX function as " spacer" elements. Am J Hum Genet, 1991,49(4) :820-838. 被引量:1
  • 8Costa JM, Ernault P, Vidaud D, et al. Fast and efficient mutation detection method using multiplex PCR and cycle sequencing-appli- cation to haemophilia B. Thromb Haemost ,2000,83 (2) :244-247. 被引量:1
  • 9Kolkman JA, Lenting P J, Mertens K. Regions 301-303 and 333-339 in the catalytic domain of blood coagulation factor Ⅸ are factor Ⅵ- Ⅱ-interactive sites involved in stimulation of enzyme activity. Bio- chem J,1999,339 ( Pt 2) :217-221. 被引量:1
  • 10Bajaj SP, Rapaport SI, Maki SL. A rnonoelonal antibody to factor Ⅸ that inhibits the factor Ⅷ :Ca potentiation of factor Ⅹ activation. J Biol Chem, 1985,260 (21) : 11574-11580. 被引量:1

二级参考文献25

  • 1戴菁,刘湘帆,王学锋,傅启华,王文斌,丁秋兰,王鸿利.中国汉族血友病B家系五种新的FⅨ基因突变的研究[J].中华检验医学杂志,2005,28(11):1117-1119. 被引量:10
  • 2Giannelli F,Green PM,High KA,et al.Haemophilia B:database of point mutations and short additions and deletions-third edition,1992.Nucleic Acids Res,1992,20:2027-2063. 被引量:1
  • 3Haemophilia B mutation database.Version 13[DB/OL].London:King's College,2004[2010-07].http://www.kcl.ac.uk/ip/petergreen/haemBdatabase.html. 被引量:1
  • 4Yoshitake S,Schach BG,Foster DC,et al.Nucleetide sequence of the gene for human factor Ⅸ (antihemophilic factor B).Biochemistry,1985,24:3736-3750. 被引量:1
  • 5Rao Z,Handford P,Mayhew M,et al.The structure of a Ca (2 +)-binding epidermal growth factor-like domain:its role in protein-protein interactions.Cell,1995,82:131-141. 被引量:1
  • 6Bode W,Brandstetter H,Mather T,et al.Comparative analysis of haemostatic proteinases:structural aspects of thrombin,factor Ⅹa,factor Ⅸa and protein C.Thromb Haemost,1997,78:501-511. 被引量:1
  • 7Celie PH,Lenting PJ,Mertens K.Hydrophobic contact between the two epidermal growth factor-like domains of blood coagulation factor Ⅸ contributes to enzymatic activity.J Biol Chem,2000,275:229-234. 被引量:1
  • 8Zhong D,Bajaj MS,Schmidt AE,et al.The N-terminal Epidermal Growth Factor-like Domain in Factor Ⅸ and Factor Ⅹ Represents an Important Recognition Motif for Binding to Tissue Factor.J Biol Chem,2002,277:3622-3631. 被引量:1
  • 9Watzke HH,Wallmark A,Hamaguchi N,et al.Factor Ⅹ Santo Domingo.Evidence that the severe clinical phenotype arises from a mutation blocking secretion.J Clin Invest,1991,88:1685-1689. 被引量:1
  • 10Sunnerhagen M,Olah GA,Stenflo J,et al.The relative orientation of Gla and EGF domains in coagulation factor Ⅹ is altered by Ca2 + binding to the first EGF domain.A combined NMR-small angle X-ray scattering study.Biochemistry,1996,35:11547-11559. 被引量:1

共引文献11

同被引文献12

  • 1王宁遂,邓兵,朱静.应用多聚酶链反应和双链DNA循环测序对FIX基因点突变的研究[J].中华血液学杂志,1995,16(5):227-228. 被引量:7
  • 2刘敬忠,向华,刘亮,周航,张纪平,石奇珍,陈怀华,曾淑燕,S.S.Sommer.应用基因扩增转录测序技术诊断乙型血友病[J].中华医学杂志,1995,75(10):599-601. 被引量:8
  • 3Mukherjee S,Mukhopadhyay A,Chaudhuri K. Analysis of haemophilia B database and strategies for identification of common point mutations in the factor Ⅸ gene[J].{H}HAEMOPHILIA,2003,(02):187-192. 被引量:1
  • 4Francisco V,Elisenda F,CarmeA. Factor Ⅸ gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B di-agnosis identification of two novelnutations[J].Br J Haematolo,2000,(02):549-551. 被引量:1
  • 5Ghosh K,Quadros L,Shetty S. Spectrum of factor Ⅸ gene mutations causing haemophilia B from India[J].{H}Blood Coagulation and Fibrinolysis,2009,(05):333-336. 被引量:1
  • 6Cooper DN,Ball EV,Stenson PD. Human Gene Mutation Database (HGMD)[OL].http:.//www.hgmd.of.ac.uk/ac/index.php,2013. 被引量:1
  • 7Belvini D,Salviato R,Radossi P. Molecular genotyping of the ltalian cohort of patients with hemophilia B[J].{H}HAEMATOLOGICA,2005,(05):635-642. 被引量:1
  • 8Mukherjee S,Mukhopadhyay A,Banerjee D. Molecular pathology of haemophilia B:identification of five novel mutations including a LINE 1 insertion in Indian patients[J].{H}HAEMOPHILIA,2004,(03):259-263. 被引量:1
  • 9Giannelli F,Green PM,Sommer SS. Haemophilia B:database of point mutations and short additions and deletions[J].{H}Nucleic Acids Research,1994,(17):3534-3546. 被引量:1
  • 10Chen SH,Zhang M,Lovrien EW. CG dinucleotide transitions in the factor Ⅸ gene account for about half of the point mutations in hemophilia B patients:a Seattle series[J].{H}Human Genetics,1991,(02):177-182. 被引量:1

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部