2. Academic Validation
  3. Asparagine 326 in the extremely C-terminal region of XRCC4 is essential for the cell survival after irradiation

Asparagine 326 in the extremely C-terminal region of XRCC4 is essential for the cell survival after irradiation

  • Biochem Biophys Res Commun. 2015 Feb 20;457(4):526-31. doi: 10.1016/j.bbrc.2015.01.015.
Rujira Wanotayan 1,  Mikoto Fukuchi 1,  Shoji Imamichi 1,  Mukesh Kumar Sharma 1,  Yoshihisa Matsumoto 2
Affiliations

Affiliations

  • 1 Research Laboratory for Nuclear Reactors and Department of Nuclear Engineering, Graduate School of Science and Engineering, Tokyo Institute of Technology, Tokyo 152-8550, Japan.
  • 2 Research Laboratory for Nuclear Reactors and Department of Nuclear Engineering, Graduate School of Science and Engineering, Tokyo Institute of Technology, Tokyo 152-8550, Japan. Electronic address: yoshim@nr.titech.ac.jp.
PMID: 25597996 DOI: 10.1016/j.bbrc.2015.01.015
Abstract

XRCC4 is one of the crucial proteins in the repair of DNA double-strand break (DSB) through non-homologous end-joining (NHEJ). As XRCC4 consists of 336 Amino acids, N-terminal 200 Amino acids include domains for dimerization and for association with DNA Ligase IV and XLF and shown to be essential for XRCC4 function in DSB repair and V(D)J recombination. On the other hand, the role of the remaining C-terminal region of XRCC4 is not well understood. In the present study, we noticed that a stretch of ∼20 Amino acids located at the extreme C-terminus of XRCC4 is highly conserved among vertebrate species. To explore its possible importance, series of mutants in this region were constructed and assessed for the functionality in terms of ability to rescue radiosensitivity of M10 cells lacking XRCC4. Among 13 mutants, M10 transfectant with N326L mutant (M10-XRCC4(N326L)) showed elevated radiosensitivity. N326L protein showed defective nuclear localization. N326L sequence matched the consensus sequence of nuclear export signal. Leptomycin B treatment accumulated XRCC4(N326L) in the nucleus but only partially rescued radiosensitivity of M10-XRCC4(N326L). These results collectively indicated that the functional defects of XRCC4(N326L) might be partially, but not solely, due to its exclusion from nucleus by synthetic nuclear export signal. Further mutation of XRCC4 Asn326 to other Amino acids, i.e., alanine, aspartic acid or glutamine did not affect the nuclear localization but still exhibited radiosensitivity. The present results indicated the importance of the extremely C-terminal region of XRCC4 and, especially, Asn326 therein.

Keywords

DNA double-strand break repair; Extremely C-terminal region; Leptomycin B; Non-homologous end-joining; Nuclear export signal; XRCC4.

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