Effect of HIV integrase inhibitors on the RAG1/2 recombinase

被引:46
作者
Melek, M
Jones, JM
O'Dea, MH
Pais, G
Burke, TR
Pommier, Y
Neamati, N
Gellert, M
机构
[1] NIDDKD, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[2] NCI, Canc Res Ctr, Med Chem Lab, Frederick, MD 21702 USA
[3] NCI, Mol Pharmacol Lab, Div Basic Sci, Bethesda, MD 20892 USA
关键词
V(D)J recombination; transposition; immune development;
D O I
10.1073/pnas.012610699
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Assembly of functional Ig and T cell receptor genes by V(D)J recombination depends on site-specific cleavage of chromosomal DNA by the RAG1/2 recombinase. As RAG1/2 action has mechanistic similarities to DNA transposases and integrases such as HIV-1 integrase, we sought to determine how integrase inhibitors of the diketo acid type would affect the various activities of RAG1/2. Both of the inhibitors we tested interfered with DNA cleavage and disintegration activities of RAG1/2, apparently by disrupting interaction with the DNA motifs bound specifically by the recombinase. The inhibitors did not ablate RAG1/2's transposition activity or capture of nonspecific transpositional target DNA, suggesting this DNA occupies a site on the recombinase different from that used for specific binding. These results further underscore the similarities between RAG1/2 and integrase and suggest that certain integrase inhibitors may have the potential to interfere with aspects of B and T cell development.
引用
收藏
页码:134 / 137
页数:4
相关论文
共 21 条
[1]   Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system [J].
Agrawal, A ;
Eastman, QM ;
Schatz, DG .
NATURE, 1998, 394 (6695) :744-751
[2]   RAG1 and RAG2 form a stable postcleavage synaptic complex with DNA containing signal ends in V(D)J recombination [J].
Agrawal, A ;
Schatz, DG .
CELL, 1997, 89 (01) :43-53
[3]   REVERSAL OF INTEGRATION AND DNA SPLICING MEDIATED BY INTEGRASE OF HUMAN-IMMUNODEFICIENCY-VIRUS [J].
CHOW, SA ;
VINCENT, KA ;
ELLISON, V ;
BROWN, PO .
SCIENCE, 1992, 255 (5045) :723-726
[4]   HIV integrase, a brief overview from chemistry to therapeutics [J].
Craigie, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :23213-23216
[5]   A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis [J].
Gao, YJ ;
Sun, Y ;
Frank, KM ;
Dikkes, P ;
Fujiwara, Y ;
Seidl, KJ ;
Sekiguchi, JM ;
Rathbun, GA ;
Swat, W ;
Wang, JY ;
Bronson, RT ;
Malynn, BA ;
Bryans, M ;
Zhu, CM ;
Chaudhuri, J ;
Davidson, L ;
Ferrini, R ;
Stamato, T ;
Orkin, SH ;
Greenberg, ME ;
Alt, FW .
CELL, 1998, 95 (07) :891-902
[6]  
Gellert M, 1997, ADV IMMUNOL, V64, P39, DOI 10.1016/S0065-2776(08)60886-X
[7]   Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: A platform for antiviral drug design [J].
Goldgur, Y ;
Craigie, R ;
Cohen, GH ;
Fujiwara, T ;
Yoshinaga, T ;
Fujishita, T ;
Sugimoto, H ;
Endo, T ;
Murai, H ;
Davies, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13040-13043
[8]   Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells [J].
Hazuda, DJ ;
Felock, P ;
Witmer, M ;
Wolfe, A ;
Stillmock, K ;
Grobler, JA ;
Espeseth, A ;
Gabryelski, L ;
Schleif, W ;
Blau, C ;
Miller, MD .
SCIENCE, 2000, 287 (5453) :646-650
[9]   DNA transposition by the RAG1 and RAG2 proteins: A possible source of oncogenic translocations [J].
Hiom, K ;
Melek, M ;
Gellert, M .
CELL, 1998, 94 (04) :463-470
[10]   Assembly of a 12/23 paired signal complex: A critical control point in V(D)J recombination [J].
Hiom, K ;
Gellert, M .
MOLECULAR CELL, 1998, 1 (07) :1011-1019