The C-terminal Domain of piggyBac Transposase Is Not Required for DNA Transposition.


Journal

Journal of molecular biology
ISSN: 1089-8638
Titre abrégé: J Mol Biol
Pays: Netherlands
ID NLM: 2985088R

Informations de publication

Date de publication:
02 04 2021
Historique:
received: 26 11 2020
accepted: 29 12 2020
pubmed: 16 1 2021
medline: 17 6 2021
entrez: 15 1 2021
Statut: ppublish

Résumé

PiggyBac(PB)-like elements (pble) are members of a eukaryotic DNA transposon family. This family is of interest to evolutionary genomics because pble transposases have been domesticated at least 9 times in vertebrates. The amino acid sequence of pble transposases can be split into three regions: an acidic N-terminal domain (~100 aa), a central domain (~400 aa) containing a DD[D/E] catalytic triad, and a cysteine-rich domain (CRD; ~90 aa). Two recent reports suggested that a functional CRD is required for pble transposase activity. Here we found that two CRD-deficient pble transposases, a PB variant and an isoform encoded by the domesticated PB-derived vertebrate transposase gene 5 (pgbd5) trigger transposition of the Ifp2 pble. When overexpressed in HeLa cells, these CRD-deficient transposases can insert Ifp2 elements with proper and improper transposon ends, associated with deleterious effects on cells. Finally, we found that mouse CRD-deficient transposase Pgbd5, as well as PB, do not insert pbles at random into chromosomes. Transposition events occurred more often in genic regions, in the neighbourhood of the transcription start sites and were often found in genes predominantly expressed in the human central nervous system.

Identifiants

pubmed: 33450253
pii: S0022-2836(20)30730-0
doi: 10.1016/j.jmb.2020.166805
pmc: PMC8426422
mid: NIHMS1730013
pii:
doi:

Substances chimiques

DNA Transposable Elements 0
Nerve Tissue Proteins 0
PGBD1 protein, human 0
PGBD5 protein, human EC 2.7.7.-
Transposases EC 2.7.7.-

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

166805

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA214812
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

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Auteurs

Laura Helou (L)

PRC, UMR INRAE 0085, CNRS 7247, Centre INRAE Val de Loire, 37380 Nouzilly, France.

Linda Beauclair (L)

PRC, UMR INRAE 0085, CNRS 7247, Centre INRAE Val de Loire, 37380 Nouzilly, France.

Hugues Dardente (H)

PRC, UMR INRAE 0085, CNRS 7247, Centre INRAE Val de Loire, 37380 Nouzilly, France.

Peter Arensburger (P)

Biological Sciences Department, California State Polytechnic University, Pomona, CA 91768, USA.

Nicolas Buisine (N)

UMR CNRS 7221, Muséum National d'Histoire Naturelle, 75005 Paris, France.

Yan Jaszczyszyn (Y)

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.

Florian Guillou (F)

PRC, UMR INRAE 0085, CNRS 7247, Centre INRAE Val de Loire, 37380 Nouzilly, France.

Thierry Lecomte (T)

EA GICC 7501, CHRU de Tours, 37044 Tours Cedex 09, France.

Alex Kentsis (A)

Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Weill Cornell Medical College, Cornell University, New York, NY, USA; Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Yves Bigot (Y)

PRC, UMR INRAE 0085, CNRS 7247, Centre INRAE Val de Loire, 37380 Nouzilly, France. Electronic address: yves.bigot@inrae.fr.

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Classifications MeSH