DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions

Author:

Buscarlet Manuel1ORCID,Provost Sylvie2,Zada Yassamin Feroz2,Barhdadi Amina2,Bourgoin Vincent1,Lépine Guylaine1,Mollica Luigina134,Szuber Natasha34,Dubé Marie-Pierre24ORCID,Busque Lambert134ORCID

Affiliation:

1. Research Centre Centre Intégré Universitaire de Santé et de Services Sociaux (CIUSSS) de l’Est-de-l’île de Montréal, Installation Hôpital Maisonneuve-Rosemont, Montreal, QC, Canada;

2. Beaulieu-Saucier Pharmacogenomics Centre, Montreal Heart Institute Research Centre, Montreal, QC, Canada;

3. Hematology Division, CIUSSS de l’Est-de-l’île de Montréal, Installation Hôpital Maisonneuve-Rosemont, Montreal, QC, Canada; and

4. Université de Montréal, Montreal, QC, Canada

Abstract

Key Points Somatic mutations driving clonal hematopoiesis occur mainly in DNMT3A and TET2 and have no significant impact on hematological phenotypes. There is a familial predisposition to acquire TET2 mutation.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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