Literature DB >> 30635825

Mosaicism of an ELANE Mutation in an Asymptomatic Mother.

Tomonari Shigemura1, Norimoto Kobayashi1, Kazunaga Agematsu2, Osamu Ohara3, Yozo Nakazawa4.   

Abstract

PURPOSE: We report normal neutrophil count in a mother, who carries the same ELANE mutation as her daughter with severe congenital neutropenia. We hypothesized that the mother possessed wild- and mutant-type clones and the wild-type clones could generate neutrophils, whereas the mutant clones could not.
METHODS: We confirmed mutant variant ratio by sequence signals and measured the frequency of the mutant allele by subcloning in various cell types. We established the ELANE-mutated and non-mutated induced pluripotent stem cells (iPSCs) from the mother's T cells and compared granulopoiesis between these iPSCs.
RESULTS: In the sequence analysis of isolated peripheral blood (PB), nail and hair, the mutant variant was detected in approximately 40-60% of lymphocytes, monocytes, hematopoietic progenitor cells, and hair as well as in a small percentage of nail, but in none of the neutrophils. In the subcloning analysis of extracted DNA from CD3+ and CD34+ cells, the mutant allele was identified in 37.5% and 38.1%, respectively. We reprogrammed the mother's PB cells and established the ELANE-mutated and non-mutated iPSCs. Granulopoiesis from mutated iPSCs revealed little sensitivity to granulocyte colony-stimulating factor in comparison with non-mutated iPSCs.
CONCLUSIONS: These observations strongly suggest that mutant-carrying neutrophils did not appear in the mother's PB because mutated clones could not differentiate into neutrophils. The mother's normal hematological phenotype could be explained by the perseverance of normal, non-mutated granulopoiesis.

Entities:  

Keywords:  ELANE gene; Severe congenital neutropenia; granulopoiesis; induced pluripotent stem cells; mosaicism

Mesh:

Substances:

Year:  2019        PMID: 30635825     DOI: 10.1007/s10875-018-0580-1

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  23 in total

1.  Novel ELANE gene mutation in a Korean girl with severe congenital neutropenia.

Authors:  Ye Jee Shim; Hee-Jin Kim; Jang Soo Suh; Kun Soo Lee
Journal:  J Korean Med Sci       Date:  2011-11-29       Impact factor: 2.153

2.  Dominantly inherited severe congenital neutropenia.

Authors:  G L Briars; H F Parry; B M Ansari
Journal:  J Infect       Date:  1996-09       Impact factor: 6.072

3.  Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes.

Authors:  Peter E Newburger; Talia N Pindyck; Zhiqing Zhu; Audrey Anna Bolyard; Andrew A G Aprikyan; David C Dale; Gary D Smith; Laurence A Boxer
Journal:  Pediatr Blood Cancer       Date:  2010-08       Impact factor: 3.167

4.  Pathogenesis of ELANE-mutant severe neutropenia revealed by induced pluripotent stem cells.

Authors:  Ramesh C Nayak; Lisa R Trump; Bruce J Aronow; Kasiani Myers; Parinda Mehta; Theodosia Kalfa; Ashley M Wellendorf; C Alexander Valencia; Patrick J Paddison; Marshall S Horwitz; H Leighton Grimes; Carolyn Lutzko; Jose A Cancelas
Journal:  J Clin Invest       Date:  2015-07-20       Impact factor: 14.808

5.  Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia patient-derived pluripotent stem cells.

Authors:  Takafumi Hiramoto; Yasuhiro Ebihara; Yoko Mizoguchi; Kazuhiro Nakamura; Kiyoshi Yamaguchi; Kazuko Ueno; Naoki Nariai; Shinji Mochizuki; Shohei Yamamoto; Masao Nagasaki; Yoichi Furukawa; Kenzaburo Tani; Hiromitsu Nakauchi; Masao Kobayashi; Kohichiro Tsuji
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

Review 6.  Pathophysiology and treatment of severe chronic neutropenia.

Authors:  K Welte; D Dale
Journal:  Ann Hematol       Date:  1996-04       Impact factor: 3.673

7.  Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia.

Authors:  Phil J Ancliff; Rosemary E Gale; Michael J Watts; Ri Liesner; Ian M Hann; Stephan Strobel; David C Linch
Journal:  Blood       Date:  2002-07-15       Impact factor: 22.113

8.  Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register.

Authors:  Christine Bellanné-Chantelot; Séverine Clauin; Thierry Leblanc; Bruno Cassinat; Fernando Rodrigues-Lima; Sandrine Beaufils; Christelle Vaury; Mohamed Barkaoui; Odile Fenneteau; Micheline Maier-Redelsperger; Christine Chomienne; Jean Donadieu
Journal:  Blood       Date:  2004-02-12       Impact factor: 22.113

Review 9.  A molecular classification of congenital neutropenia syndromes.

Authors:  Laurence A Boxer; Peter E Newburger
Journal:  Pediatr Blood Cancer       Date:  2007-10-15       Impact factor: 3.167

10.  Neutropenia-associated ELANE mutations disrupting translation initiation produce novel neutrophil elastase isoforms.

Authors:  Timothy Tidwell; Jeremy Wechsler; Ramesh C Nayak; Lisa Trump; Stephen J Salipante; Jerry C Cheng; Jean Donadieu; Taly Glaubach; Seth J Corey; H Leighton Grimes; Carolyn Lutzko; Jose A Cancelas; Marshall S Horwitz
Journal:  Blood       Date:  2013-11-01       Impact factor: 22.113

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  2 in total

Review 1.  Congenital neutropenia: disease models guiding new treatment strategies.

Authors:  Ivo P Touw
Journal:  Curr Opin Hematol       Date:  2022-01-01       Impact factor: 3.284

2.  Low frequency of treatable pediatric disease alleles in gnomAD: An opportunity for future genomic screening of newborns.

Authors:  Nina B Gold; Steven M Harrison; Jared H Rowe; Jessica Gold; Elissa Furutani; Alessandra Biffi; Christine N Duncan; Akiko Shimamura; Leslie E Lehmann; Robert C Green
Journal:  HGG Adv       Date:  2021-09-25
  2 in total

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