2. Academic Validation
  3. Pharmacological inhibition of neddylation impairs long interspersed element 1 retrotransposition

Pharmacological inhibition of neddylation impairs long interspersed element 1 retrotransposition

  • Cell Rep. 2024 Feb 27;43(2):113749. doi: 10.1016/j.celrep.2024.113749.
Yan Li 1,  Siyu Shen 2,  Haoran Guo 2,  Huili Li 2,  Lili Zhang 2,  Boyin Zhang 3,  Xiao-Fang Yu 4,  Wei Wei 5
Affiliations

Affiliations

  • 1 Key Laboratory of Organ Regeneration and Transplantation of Ministry of Education, Institute of Translational Medicine, First Hospital, Jilin University, Changchun, Jilin 130021, China; Department of Pathology, The First Bethune Hospital of Jilin University, Changchun, China.
  • 2 Key Laboratory of Organ Regeneration and Transplantation of Ministry of Education, Institute of Translational Medicine, First Hospital, Jilin University, Changchun, Jilin 130021, China.
  • 3 Department of Orthopedics Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
  • 4 Cancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310000, China; Cancer Center, Zhejiang University, Hangzhou, Zhejiang 310000, China.
  • 5 Key Laboratory of Organ Regeneration and Transplantation of Ministry of Education, Institute of Translational Medicine, First Hospital, Jilin University, Changchun, Jilin 130021, China; Institute of Virology and AIDS Research, First Hospital, Jilin University, Changchun, Jilin 130021, China. Electronic address: [email protected].
PMID: 38329876 DOI: 10.1016/j.celrep.2024.113749
Abstract

Aberrant long interspersed element 1 (LINE-1 or L1) activity can cause insertional mutagenesis and chromosomal rearrangements and has been detected in several types of cancers. Here, we show that neddylation, a post-translational modification process, is essential for L1 transposition. The antineoplastic drug MLN4924 is an L1 inhibitor that suppresses NEDD8-activating Enzyme activity. Neddylation inhibition by MLN4924 selectively impairs ORF2p-mediated L1 reverse transcription and blocks the generation of L1 cDNA. Consistent with these results, MLN4924 treatment suppresses the retrotransposition activity of the non-autonomous retrotransposons short interspersed nuclear element R/variable number of tandem repeat/Alu and Alu, which rely on the reverse transcription activity of L1 ORF2p. The E2 Enzyme UBE2M in the neddylation pathway, rather than UBE2F, is required for L1 ORF2p and retrotransposition. Interference with the functions of certain neddylation-dependent Cullin-really interesting new gene E3 Ligases disrupts L1 reverse transcription and transposition activity. Our findings provide insights into the regulation of L1 retrotransposition and the identification of therapeutic targets for L1 dysfunctions.

Keywords

CP: Molecular biology; LINE-1; MLN4924; UBE2M; neddylation; retrotransposition.

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