Somatic genetic rescue in Mendelian haematopoietic diseases

被引:77
|
作者
Revy, Patrick [1 ,2 ]
Kannengiesser, Caroline [3 ,4 ]
Fischer, Alain [2 ,5 ,6 ,7 ]
机构
[1] INSERM UMR 1163, Equipe Labellisee Ligue Canc, Lab Genome Dynam Immune Syst, F-1163 Paris, France
[2] Sorbonne Paris Cite Univ, Imagine Inst, Paris Descartes, Paris, France
[3] Hop Bichat Claude Bernard, AP HP, Serv Genet, Paris, France
[4] Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
[5] Coll France, Chaire Med Expt, Paris, France
[6] Hop Necker Enfants Malad, AP HP, Unite Immunol Hematol & Rhumatol Pediat, Paris, France
[7] INSERM UMR 1163, Imagine Inst, Paris, France
关键词
TERT PROMOTER MUTATIONS; SEVERE COMBINED IMMUNODEFICIENCY; WISKOTT-ALDRICH-SYNDROME; IN-VIVO REVERSION; DETECTABLE CLONAL MOSAICISM; SHWACHMAN-DIAMOND SYNDROME; FANCONI-ANEMIA PATIENT; BONE-MARROW FAILURE; T-CELL DEVELOPMENT; MATERNAL T;
D O I
10.1038/s41576-019-0139-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Somatic mutations occur spontaneously in normal individuals and accumulate throughout life. These genetic modifications contribute to progressive ageing phenotypes and are directly involved in cancer development. However, a growing number of studies of Mendelian haematopoietic disorders indicate that somatic genetic events can offset the pathogenic effect of germline mutations at the cellular level, leading to genetic mosaicism and, in some cases, resulting in a milder disease phenotype. Notably, spontaneous genetic events that confer a positive effect on cells do not always benefit the individual, for whom the effects can be neutral or even clinically detrimental. These somatic genetic rescue events have important diagnostic, therapeutic and clinical consequences and constitute valuable models for studying the differentiation and/or homeostasis of haematopoietic lineages.
引用
收藏
页码:582 / 598
页数:17
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