Cyclic Neutropenia From a Novel Mutation Ala57Asp of ELANE: Phenotypic Variability in Neutropenia From Mutated Ala57 Residue

被引:3
作者
Park, Chang-Hun [1 ,5 ]
Park, Silvia [2 ,4 ]
Kim, Yae-Jean [3 ]
Kim, Sun-Hee [1 ]
Kim, Hee-Jin [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Lab Med & Genet, Sch Med, 81 Irwon Ro, Seoul 06351, South Korea
[2] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Sch Med, Seoul, South Korea
[3] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pediat, Sch Med, Seoul, South Korea
[4] Catholic Univ Korea, Dept Hematol, Catholic Hematol Hosp, Seoul St Marys Hosp,Coll Med, Seoul, Seoul, South Korea
[5] Sungkyunkwan Univ, Sch Med, Dept Lab Med & Genet, Samsung Changwon Hosp, Chang Won, South Korea
关键词
ELANE-related neutropenia; cyclic neutropenia; Ala57Asp; mutation; SEVERE CONGENITAL NEUTROPENIA; ELASTASE; GENE;
D O I
10.1097/MPH.0000000000001353
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ELANE-related neutropenia includes severe congenital neutropenia and cyclic neutropenia. Both are clinically characterized by recurrent fever, skin and oropharyngeal inflammation. We report a novel mutation in ELANE in a 20-year-old man with a history of self-limiting febrile episodes and neutropenia with a cyclic pattern since 7 years of age. Direct sequencing analysis of ELANE revealed he was heterozygous for a novel missense mutation (p.Ala57Asp). The Ala57 residue is a mutation hotspot, and all previously reported missense mutations (Ala57Ser/Thr/Val) were observed in severe congenital neutropenia cases. Thus, the present case demonstrates a phenotypic variability in ELANE-related neutropenia from mutated Ala57.
引用
收藏
页码:E231 / E234
页数:4
相关论文
共 16 条
  • [1] Mutations in the ELA2 gene correlate with more severe expression of neutropenia:: a study of 81 patients from the French Neutropenia Register
    Bellanné-Chantelot, C
    Clauin, S
    Leblanc, T
    Cassinat, B
    Rodrigues-Lima, F
    Beaufils, S
    Vaury, C
    Barkaoui, M
    Fenneteau, O
    Maier-Redelsperger, M
    Chomienne, C
    Donadieu, J
    [J]. BLOOD, 2004, 103 (11) : 4119 - 4125
  • [2] A molecular classification of congenital neutropenia syndromes
    Boxer, Laurence A.
    Newburger, Peter E.
    [J]. PEDIATRIC BLOOD & CANCER, 2007, 49 (05) : 609 - 614
  • [3] Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
    Dale, DC
    Person, RE
    Bolyard, AA
    Aprikyan, AG
    Bos, C
    Bonilla, MA
    Boxer, LA
    Kannourakis, G
    Zeidler, C
    Welte, K
    Benson, KF
    Horwitz, M
    [J]. BLOOD, 2000, 96 (07) : 2317 - 2322
  • [4] Dale DC, 2011, ELANE RELATED NEUTRO
  • [5] Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis
    Grenda, David S.
    Murakami, Mark
    Ghatak, Jhuma
    Xia, Jun
    Boxer, Laurence A.
    Dale, David
    Dinauer, Mary C.
    Link, Daniel C.
    [J]. BLOOD, 2007, 110 (13) : 4179 - 4187
  • [6] SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling
    Guex, N
    Peitsch, MC
    [J]. ELECTROPHORESIS, 1997, 18 (15) : 2714 - 2723
  • [7] Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis
    Horwitz, M
    Benson, KF
    Person, RE
    Aprikyan, AG
    Dale, DC
    [J]. NATURE GENETICS, 1999, 23 (04) : 433 - 436
  • [8] IMPROVED METHODS FOR BUILDING PROTEIN MODELS IN ELECTRON-DENSITY MAPS AND THE LOCATION OF ERRORS IN THESE MODELS
    JONES, TA
    ZOU, JY
    COWAN, SW
    KJELDGAARD, M
    [J]. ACTA CRYSTALLOGRAPHICA SECTION A, 1991, 47 : 110 - 119
  • [9] A lack of secretory leukocyte protease inhibitor (SLPI) causes defects in granulocytic differentiation
    Klimenkova, Olga
    Ellerbeck, Wienke
    Klimiankou, Maksim
    Uenalan, Murat
    Kandabarau, Siarhei
    Gigina, Anna
    Hussein, Kais
    Zeidler, Cornelia
    Welte, Karl
    Skokowa, Julia
    [J]. BLOOD, 2014, 123 (08) : 1239 - 1249
  • [10] Mutations in neutrophil elastase causing congenital neutropenia lead to cytoplasmic protein accumulation and induction of the unfolded protein response
    Koellner, Inga
    Socleik, Beate
    Schreek, Sabine
    Heyn, Holger
    von Neuhoff, Nils
    Germeshausen, Manuela
    Zeidler, Cornelia
    Krueger, Martin
    Schlegelberger, Brigitte
    Welte, Karl
    Beger, Carmela
    [J]. BLOOD, 2006, 108 (02) : 493 - 500