Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

被引:188
作者
Albers, Cornelis A. [1 ,2 ]
Cvejic, Ana [1 ,2 ]
Favier, Remi [3 ,4 ]
Bouwmans, Evelien E. [2 ]
Alessi, Marie-Christine [5 ]
Bertone, Paul [6 ]
Jordan, Gregory [6 ]
Kettleborough, Ross N. W. [1 ]
Kiddle, Graham [2 ]
Kostadima, Myrto [6 ]
Read, Randy J. [7 ]
Sipos, Botond [6 ]
Sivapalaratnam, Suthesh [8 ]
Smethurst, Peter A. [2 ]
Stephens, Jonathan [2 ]
Voss, Katrin [2 ]
Nurden, Alan [9 ]
Rendon, Augusto [2 ,10 ]
Nurden, Paquita [9 ]
Ouwehand, Willem H. [1 ,2 ]
机构
[1] Wellcome Trust Sanger Inst, Cambridge, England
[2] NHS Blood & Transplant, Cambridge, England
[3] Hop Armand Trousseau, AP HP, Dept Hematol, Ctr Reference Pathol Plaquettaires, Paris, France
[4] INSERM, U1009, Villejuif, France
[5] INSERM, U626, Fac Med, F-13258 Marseille, France
[6] European Bioinformat Inst, European Mol Biol Lab, Cambridge, England
[7] Univ Cambridge, Dept Haematol, Cambridge Inst Med Res, Cambridge, England
[8] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
[9] Hop Xavier Arnozan, Ctr Reference Pathol Plaquettaires, Hematol Lab, Pessac, France
[10] Inst Publ Hlth, Med Res Council Biostat Unit, Cambridge, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
CHEDIAK-HIGASHI-SYNDROME;
D O I
10.1038/ng.885
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gray platelet syndrome (GPS) is a predominantly recessive platelet disorder that is characterized by mild thrombocytopenia with large platelets and a paucity of alpha-granules; these abnormalities cause mostly moderate but in rare cases severe bleeding. We sequenced the exomes of four unrelated individuals and identified NBEAL2 as the causative gene; it has no previously known function but is a member of a gene family that is involved in granule development. Silencing of nbeal2 in zebrafish abrogated thrombocyte formation.
引用
收藏
页码:735 / 737
页数:3
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