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TRAF6 mediates human DNA2 polyubiquitination and nuclear localization to maintain nuclear genome integrity
Author(s) -
Yuan Meng,
Changwei Liu,
Lei Shen,
Mian Zhou,
Wenpeng Liu,
Claudia Kowolik,
Judith L. Campbell,
Li Zheng,
Binghui Shen
Publication year - 2019
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkz537
Subject(s) - biology , nuclear localization sequence , microbiology and biotechnology , helicase , nuclease , dna repair , ubiquitin , ubiquitin ligase , dna replication , dna damage , nuclear export signal , genetics , cell nucleus , dna , nucleus , gene , rna
The multifunctional human DNA2 (hDNA2) nuclease/helicase is required to process DNA ends for homology-directed recombination repair (HDR) and to counteract replication stress. To participate in these processes, hDNA2 must localize to the nucleus and be recruited to the replication or repair sites. However, because hDNA2 lacks the nuclear localization signal that is found in its yeast homolog, it is unclear how its migration into the nucleus is regulated during replication or in response to DNA damage. Here, we report that the E3 ligase TRAF6 binds to and mediates the K63-linked polyubiquitination of hDNA2, increasing the stability of hDNA2 and promoting its nuclear localization. Inhibiting TRAF6-mediated polyubiquitination abolishes the nuclear localization of hDNA2, consequently impairing DNA end resection and HDR. Thus, the current study reveals a mechanism for the regulation of hDNA2 localization and establishes that TRAF6-mediated hDNA2 ubiquitination activates DNA repair pathways to maintain nuclear genome integrity.

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