DDX41: exploring the roles of a versatile helicase

被引:2
作者
Winstone, Lacey [1 ]
Jung, Yohan [1 ]
Wu, Yuliang [1 ]
机构
[1] Univ Saskatchewan, Dept Biochem Microbiol & Immunol, Saskatoon, SK S7N 5E5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ACUTE MYELOID-LEUKEMIA; I IFN PRODUCTION; CYCLIC-DI-AMP; FUNCTIONAL-CHARACTERIZATION; R-LOOP; FAMILY; MUTATIONS; VARIANTS; SENSOR; EXPRESSION;
D O I
10.1042/BST20230725
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DDX41 is a DEAD-box helicase and is conserved across species. Mutations in DDX41 have been associated with myeloid neoplasms, including myelodysplastic syndrome and acute myeloid leukemia. Though its pathogenesis is not completely known, DDX41 has been shown to have many cellular roles, including in pre-mRNA splicing, innate immune sensing, ribosome biogenesis, translational regulation, and R -loop metabolism. In this review, we will summarize the latest understandings regarding the various roles of DDX41, as well as highlight challenges associated with drug development to target DDX41. Overall, understanding the molecular and cellular mechanisms of DDX41 could help develop novel therapeutic options for DDX41 mutation-related hematologic malignancies.
引用
收藏
页码:395 / 405
页数:11
相关论文
共 50 条
  • [31] Clinical features of DDX41 mutation-related diseases: a systematic review with individual patient data
    Wan, Ziqi
    Han, Bing
    THERAPEUTIC ADVANCES IN HEMATOLOGY, 2021, 12
  • [32] The DEAD-box RNA helicase DDX41 is a novel repressor of p21WAF1/CIP1 mRNA translation
    Peters, Dominik
    Radine, Claudia
    Reese, Alina
    Budach, Wilfried
    Sohn, Dennis
    Jaenicke, Reiner U.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2017, 292 (20) : 8331 - 8341
  • [33] Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia
    Cardoso, S. R.
    Ryan, G.
    Walne, A. J.
    Ellison, A.
    Lowe, R.
    Tummala, H.
    Rio-Machin, A.
    Collopy, L.
    Al Seraihi, A.
    Wallis, Y.
    Page, P.
    Akiki, S.
    Fitzgibbon, J.
    Vulliamy, T.
    Dokal, I.
    LEUKEMIA, 2016, 30 (10) : 2083 - 2086
  • [34] Grouper DDX41 exerts antiviral activity against fish iridovirus and nodavirus infection
    Liu, Jiaxin
    Huang, Youhua
    Huang, Xiaohong
    Li, Chen
    Ni, Song Wei
    Yu, Yepin
    Qin, Qiwei
    FISH & SHELLFISH IMMUNOLOGY, 2019, 91 : 40 - 49
  • [35] Clinical and molecular correlates of somatic and germline DDX41 variants in patients and families with myeloid neoplasms
    Badar, Talha
    Nanaa, Ahmad
    Foran, James M.
    Viswanatha, David
    Al-Kali, Aref
    Lasho, Terra
    Finke, Christy
    Alkhateeb, Hassan B.
    He, Rong
    Gangat, Naseema
    Shah, Mithun
    Tefferi, Ayalew
    Mangaonkar, Abhishek A.
    Litzow, Mark R.
    Ongie, Laura J.
    Chlon, Timothy
    Ferrer, Alejandro
    Patnaik, Mrinal M.
    HAEMATOLOGICA, 2023, 108 (11) : 3033 - 3043
  • [36] Germline DDX41 mutations define a significant entity within adult MDS/AML patients
    Sebert, Marie
    Passet, Marie
    Raimbault, Anna
    Rahme, Ramy
    Raffoux, Emmanuel
    de Fontbrune, Flore Sicre
    Cerrano, Marco
    Quentin, Samuel
    Vasquez, Nadia
    Da Costa, Melanie
    Boissel, Nicolas
    Dombret, Herve
    de Latour, Regis Peffault
    Socie, Gerard
    Itzykson, Raphael
    Fenaux, Pierre
    Soulier, Jean
    Ades, Lionel
    Clappier, Emmanuelle
    BLOOD, 2019, 134 (17) : 1441 - 1444
  • [37] Multifunctional role of DEAD-box helicase 41 in innate immunity, hematopoiesis and disease
    Ma, Jing
    Ross, Susan R.
    FRONTIERS IN IMMUNOLOGY, 2024, 15
  • [38] The helicase DDX41 recognizes the bacterial secondary messengers cyclic di-GMP and cyclic di-AMP to activate a type I interferon immune response
    Parvatiyar, Kislay
    Zhang, Zhiqiang
    Teles, Rosane M.
    Ouyang, Songying
    Jiang, Yan
    Iyer, Shankar S.
    Zaver, Shivam A.
    Schenk, Mirjam
    Zeng, Shang
    Zhong, Wenwan
    Liu, Zhi-Jie
    Modlin, Robert L.
    Liu, Yong-jun
    Cheng, Genhong
    NATURE IMMUNOLOGY, 2012, 13 (12) : 1155 - +
  • [39] DDX41 mutations in myeloid neoplasms are associated with male gender, TP53 mutations and high-risk disease
    Quesada, Andres E.
    Routbort, Mark J.
    DiNardo, Courtney D.
    Bueso-Ramos, Carlos E.
    Kanagal-Shamanna, Rashmi
    Khoury, Joseph D.
    Thakral, Beenu
    Zuo, Zhuang
    Yin, C. Cameron
    Loghavi, Sanam
    Ok, Chi Y.
    Wang, Sa A.
    Tang, Zhenya
    Bannon, Sarah A.
    Benton, Christopher B.
    Garcia-Manero, Guillermo
    Kantarjian, Hagop
    Luthra, Rajyalakshmi
    Medeiros, L. Jeffrey
    Patel, Keyur P.
    AMERICAN JOURNAL OF HEMATOLOGY, 2019, 94 (07) : 757 - 766
  • [40] Novel germline missense DDX41 variant in a patient with an adult-onset myeloid neoplasm with excess blasts without dysplasia
    Pinto e Vairo, Filippo
    Ferrer, Alejandro
    Cathcart-Rake, Elizabeth
    King, Rebecca L.
    Howard, Matthew T.
    Viswanatha, David S.
    Klee, Eric W.
    Mangaonkar, Abhishek A.
    Patnaik, Mrinal M.
    LEUKEMIA & LYMPHOMA, 2019, 60 (05) : 1337 - 1339