Literature DB >> 22972950

Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia.

Maartje Nielsen1, Clementien L Vermont, Emmelien Aten, Claudia A L Ruivenkamp, Femke van Herrewegen, Gijs W E Santen, Martijn H Breuning.   

Abstract

BACKGROUND: Gene-targeting studies in mice have revealed a key role for EVI1 protein in the maintenance of haematopoiesis, and argue in favour of a gene dosage requirement for EVI1 in the regulation of haematopoietic stem cells. Furthermore, a fusion transcript of MDS1 and EVI1 has been shown to play a critical role in maintaining long-term haematopoietic stem cell function. Inappropriate activation of EVI1, usually due to a translocation, is a well known and unfavourable change in several myeloid malignancies. It is not known whether haploinsufficiency of any of these genes leads to disease in humans.
METHODS: SNP array analysis in a patient with in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia RESULTS AND
CONCLUSIONS: We report for the first time a constitutional deletion encompassing the EVI1 and MDS1 genes in a human, and argue that the deletion causes congenital bone marrow failure in this patient.

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Year:  2012        PMID: 22972950     DOI: 10.1136/jmedgenet-2012-100990

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 in total

1.  Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3' MECOM.

Authors:  Lars T van der Veken; Merel C Maiburg; Floris Groenendaal; Mariëlle E van Gijn; Andries C Bloem; Claudia Erpelinck; Stefan Gröschel; Mathijs A Sanders; Ruud Delwel; Marc B Bierings; Arjan Buijs
Journal:  Haematologica       Date:  2018-02-08       Impact factor: 9.941

2.  Expanding the phenotypic and genetic spectrum of radioulnar synostosis associated hematological disease.

Authors:  Amanda Walne; Hemanth Tummala; Alicia Ellison; Shirleny Cardoso; Jasmin Sidhu; Gabriela Sciuccati; Tom Vulliamy; Inderjeet Dokal
Journal:  Haematologica       Date:  2018-03-08       Impact factor: 9.941

3.  MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies.

Authors:  Tim Ripperger; Winfried Hofmann; Jan C Koch; Katayoon Shirneshan; Detlef Haase; Gerald Wulf; Peter R Issing; Matthias Karnebogen; Gunnar Schmidt; Bernd Auber; Brigitte Schlegelberger; Thomas Illig; Birgit Zirn; Doris Steinemann
Journal:  Haematologica       Date:  2017-11-02       Impact factor: 9.941

Review 4.  Hematopoietic transcription factor mutations: important players in inherited platelet defects.

Authors:  Natthapol Songdej; A Koneti Rao
Journal:  Blood       Date:  2017-04-17       Impact factor: 22.113

5.  MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.

Authors:  Manuela Germeshausen; Phil Ancliff; Jaime Estrada; Markus Metzler; Eva Ponstingl; Horst Rütschle; Dirk Schwabe; Richard H Scott; Sule Unal; Angela Wawer; Bernward Zeller; Matthias Ballmaier
Journal:  Blood Adv       Date:  2018-03-27

6.  A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome.

Authors:  Miriam Coelho Molck; Milena Simioni; Társis Paiva Vieira; Fabíola Paoli Monteiro; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2018-06-08

7.  Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.

Authors:  Tetsuya Niihori; Meri Ouchi-Uchiyama; Yoji Sasahara; Takashi Kaneko; Yoshiko Hashii; Masahiro Irie; Atsushi Sato; Yuka Saito-Nanjo; Ryo Funayama; Takeshi Nagashima; Shin-Ichi Inoue; Keiko Nakayama; Keiichi Ozono; Shigeo Kure; Yoichi Matsubara; Masue Imaizumi; Yoko Aoki
Journal:  Am J Hum Genet       Date:  2015-11-12       Impact factor: 11.025

Review 8.  Overview of inherited bone marrow failure syndromes.

Authors:  Meerim Park
Journal:  Blood Res       Date:  2022-04-30
  8 in total

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