Structural insights into the duplex DNA processing of TREX2. Issue 22 (24th October 2018)

• Record Type: Journal Article
• Authors: Cheng, Hiu-Lo; Lin, Chun-Ting; Huang, Kuan-Wei; Wang, Shuying; Lin, Yeh-Tung; Toh, Shu-Ing; Hsiao, Yu-Yuan
• Is Part Of: Nucleic acids research. Volume 46:Issue 22(2018)
• Page Start: 12166
• Page End: 12176
• Publication Date: 2018-10-24
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gky970
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: The t hree prime r epair ex onuclease 2 (TREX2) is an essential 3′-to-5′ exonuclease that functions in cell proliferation, genome integrity and skin homeostasis maintenance. The abnormal expression level of TREX2 can result in broken chromosome, increased susceptibility to skin carcinogenesis and Psoriasis. However, the molecular mechanisms of how TREX2 binds and processes its natural substrates, dsDNA or chromosomal DNA, to maintain genome stability remain unclear. In this study, we present four new crystal structures: apo-TREX2, TREX2 in complex with two different dsDNA substrates, and TREX2 in complex with a processed dsDNA product. Analysis of the structures reveals that TREX2 stacks with the 5′-terminal of dsDNA by a Leu20-Pro21-Asn22 cluster for precisely trimming the 3′-overhang. In addition, TREX2 specifically interacts with the non-scissile strand of dsDNA by an α-helix-loop region. The unique interaction patterns of the TREX2–dsDNA complex highlight the requirement of long double-stranded region for TREX2 binding and provide evidence of the functional role of TREX2 in processing chromosomal DNA. Moreover, the non-processive property of TREX2 is elucidated by the structure of TREX2–product complex. Our work discloses the first structural basis of the molecular interactions between TREX2 and its substrates and unravels the mechanistic actions of TREX2.