Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms. Academic Article uri icon

Overview

abstract

  • Most cases of adult myeloid neoplasms are routinely assumed to be sporadic. Here, we describe an adult familial acute myeloid leukemia (AML) syndrome caused by germline mutations in the DEAD/H-box helicase gene DDX41. DDX41 was also found to be affected by somatic mutations in sporadic cases of myeloid neoplasms as well as in a biallelic fashion in 50% of patients with germline DDX41 mutations. Moreover, corresponding deletions on 5q35.3 present in 6% of cases led to haploinsufficient DDX41 expression. DDX41 lesions caused altered pre-mRNA splicing and RNA processing. DDX41 is exemplary of other RNA helicase genes also affected by somatic mutations, suggesting that they constitute a family of tumor suppressor genes.

authors

  • Polprasert, Chantana
  • Schulze, Isabell
  • Sekeres, Mikkael A
  • Makishima, Hideki
  • Przychodzen, Bartlomiej
  • Hosono, Naoko
  • Singh, Jarnail
  • Padgett, Richard A
  • Gu, Xiaorong
  • Phillips, James G
  • Clemente, Michael
  • Parker, Yvonne
  • Lindner, Daniel
  • Dienes, Brittney
  • Jankowsky, Eckhard
  • Saunthararajah, Yogen
  • Du, Yang
  • Oakley, Kevin
  • Nguyen, Nhu
  • Mukherjee, Sudipto
  • Pabst, Caroline
  • Godley, Lucy A
  • Churpek, Jane E
  • Pollyea, Daniel A
  • Krug, Utz
  • Berdel, Wolfgang E
  • Klein, Hans-Ulrich
  • Dugas, Martin
  • Shiraishi, Yuichi
  • Chiba, Kenichi
  • Tanaka, Hiroko
  • Miyano, Satoru
  • Yoshida, Kenichi
  • Ogawa, Seishi
  • Müller-Tidow, Carsten
  • Maciejewski, Jaroslaw P

publication date

  • April 23, 2015

Research

keywords

  • DEAD-box RNA Helicases
  • Germ-Line Mutation
  • Leukemia, Myeloid, Acute

Identity

PubMed Central ID

  • PMC8713504

Scopus Document Identifier

  • 84929167143

Digital Object Identifier (DOI)

  • 10.1016/j.ccell.2015.03.017

PubMed ID

  • 25920683

Additional Document Info

volume

  • 27

issue

  • 5