Dissection of affinity captured LINE-1 macromolecular complexes

Author:

Taylor Martin S1ORCID,Altukhov Ilya2ORCID,Molloy Kelly R3,Mita Paolo4ORCID,Jiang Hua5,Adney Emily M46,Wudzinska Aleksandra6,Badri Sana7,Ischenko Dmitry2,Eng George1,Burns Kathleen H58ORCID,Fenyö David4ORCID,Chait Brian T3,Alexeev Dmitry9ORCID,Rout Michael P5,Boeke Jef D4ORCID,LaCava John45ORCID

Affiliation:

1. Department of Pathology, Massachusetts General Hospital, Boston, United States

2. Moscow Institute of Physics and Technology, Dolgoprudny, Russia

3. Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, United States

4. Department of Biochemistry and Molecular Pharmacology, Institute for Systems Genetics, NYU Langone Health, New York, United States

5. Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, United States

6. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, United States

7. Department of Pathology, NYU Langone Health, New York, United States

8. Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, United States

9. Novosibirsk State University, Novosibirsk, Russia

Abstract

Long Interspersed Nuclear Element-1 (LINE-1, L1) is a mobile genetic element active in human genomes. L1-encoded ORF1 and ORF2 proteins bind L1 RNAs, forming ribonucleoproteins (RNPs). These RNPs interact with diverse host proteins, some repressive and others required for the L1 lifecycle. Using differential affinity purifications, quantitative mass spectrometry, and next generation RNA sequencing, we have characterized the proteins and nucleic acids associated with distinctive, enzymatically active L1 macromolecular complexes. Among them, we describe a cytoplasmic intermediate that we hypothesize to be the canonical ORF1p/ORF2p/L1-RNA-containing RNP, and we describe a nuclear population containing ORF2p, but lacking ORF1p, which likely contains host factors participating in target-primed reverse transcription.

Funder

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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