Differential assembly of Rous sarcoma virus tetrameric and octameric intasomes is regulated by the C-terminal domain and tail region of integrase

• Published in: The Journal of biological chemistry 2018-10, Vol.293 (42), p.16440-16452
• Main Authors: Bera, Sibes, Pandey, Krishan K., Aihara, Hideki, Grandgenett, Duane P.
• Format: Article
• Language: English
• Subjects: Animals; DNA enzyme; DNA, Viral - metabolism; DNA–protein interaction; Enzymology; HIV; human immunodeficiency virus (HIV); intasome; integrase; integrase tetrameric and octameric stable synaptic complex; Integrases - chemistry; Integrases - metabolism; Protein Multimerization; retrovirus; Rous sarcoma virus; Rous sarcoma virus - chemistry; strand-transfer complex; strand-transfer inhibitors; Terminal Repeat Sequences; viral integration; Virus Integration
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.RA118.004768

Retrovirus integrase (IN) catalyzes the concerted integration of linear viral DNA ends into chromosomes. The atomic structures of five different retrovirus IN–DNA complexes, termed intasomes, have revealed varying IN subunit compositions ranging from tetramers to octamers, dodecamers, and hexadecamers. Intasomes containing two IN-associated viral DNA ends capable of concerted integration are termed stable synaptic complexes (SSC), and those formed with a viral/target DNA substrate representing the product of strand-transfer reactions are strand-transfer complexes (STC). Here, we investigated the mechanisms associated with the assembly of the Rous sarcoma virus SSC and STC. C-terminal truncations of WT IN (286 residues) indicated a role of the last 18 residues (“tail” region) in assembly of the tetrameric and octameric SSC, physically stabilized by HIV-1 IN strand-transfer inhibitors. Fine mapping through C-terminal truncations and site-directed mutagenesis suggested that at least three residues (Asp-268–Thr-270) past the last β-strand in the C-terminal domain (CTD) are necessary for assembly of the octameric SSC. In contrast, the assembly of the octameric STC was independent of the last 18 residues of IN. Single-site substitutions in the CTD affected the assembly of the SSC, but not necessarily of the STC, suggesting that STC assembly may depend less on specific interactions of the CTD with viral DNA. Additionally, we demonstrate that trans-communication between IN dimer–DNA complexes facilitates the association of native long-terminal repeat (LTR) ends with partially defective LTR ends to produce a hybrid octameric SSC. The differential assembly of the tetrameric and octameric SSC improves our understanding of intasomes.