Interaction networks of the molecular machines that decode, replicate, and maintain the integrity of the human genome

被引:15
作者
Coulombe, B [1 ]
Jeronimo, C [1 ]
Langelier, MF [1 ]
Cojocaru, M [1 ]
Bergeron, D [1 ]
机构
[1] Inst Rech Clin Montreal, Lab Gene Transcript, Montreal, PQ H2W 1R7, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1074/mcp.R400009-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The interaction of many proteins with genomic DNA is required for the expression, replication, and maintenance of the integrity of mammalian genomes. These proteins participate in processes as diverse as gene transcription and mRNA processing, as well as in DNA replication, recombination, and repair. This intricate system, where the various nuclear machineries interact with one another and bind to either common or distinct DNA regions to create an impressive network of protein-protein and protein-DNA interactions, is made even more complex by the need for a very stringent control in order to ensure normal cell growth and differentiation. A general methodology based on the in vivo pull-down of tagged components of nuclear machines and regulatory proteins was used to study genome-wide protein-protein and protein-DNA interactions in mammalian cells. In particular, this approach has been used in defining the interaction networks ( or "interactome") formed by RNA polymerase II, a molecular machine that decodes the human genome. In addition, because this methodology allows for the purification of variant forms of tagged complexes having site-directed mutations in key elements, it can also be used for deciphering the relationship between the structure and the function of the molecular machines, such as RNA polymerase II, that by binding DNA play a central role in the pathway from the genome to the organism.
引用
收藏
页码:851 / 856
页数:6
相关论文
共 33 条
[1]   FCP1, the RAP74-interacting subunit of a human protein phosphatase that dephosphorylates the carboxyl-terminal domain of RNA polymerase IIO [J].
Archambault, J ;
Pan, GH ;
Dahmus, GK ;
Cartier, M ;
Marshall, N ;
Zhang, S ;
Dahmus, ME ;
Greenblatt, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) :27593-27601
[2]  
BUSHNELL DA, 2003, P NATL ACAD SCI US
[3]  
CAREY M, 2000, TRANSCRIPTIONAL REGU
[4]   DNA bending and wrapping around RNA polymerase: A "revolutionary" model describing transcriptional mechanisms [J].
Coulombre, B ;
Burton, ZF .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1999, 63 (02) :457-+
[5]   Bridging structural biology and genomics: assessing protein interaction data with known complexes [J].
Edwards, AM ;
Kus, B ;
Jansen, R ;
Greenbaum, D ;
Greenblatt, J ;
Gerstein, M .
TRENDS IN GENETICS, 2002, 18 (10) :529-536
[6]   A NOVEL GENETIC SYSTEM TO DETECT PROTEIN PROTEIN INTERACTIONS [J].
FIELDS, S ;
SONG, OK .
NATURE, 1989, 340 (6230) :245-246
[7]   RAP74 induces promoter contacts by RNA polymerase II upstream and downstream of a DNA bend centered on the TATA box [J].
Forget, D ;
Robert, F ;
Grondin, G ;
Burton, ZF ;
Greenblatt, J ;
Coulombe, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7150-7155
[8]   Photo-cross-linking of a purified preinitiation complex reveals central roles for the RNA polymerase II mobile clamp and TFIIE in initiation mechanisms [J].
Forget, D ;
Langelier, MF ;
Thérien, C ;
Trinh, V ;
Coulombe, B .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (03) :1122-1131
[9]   Functional organization of the yeast proteome by systematic analysis of protein complexes [J].
Gavin, AC ;
Bösche, M ;
Krause, R ;
Grandi, P ;
Marzioch, M ;
Bauer, A ;
Schultz, J ;
Rick, JM ;
Michon, AM ;
Cruciat, CM ;
Remor, M ;
Höfert, C ;
Schelder, M ;
Brajenovic, M ;
Ruffner, H ;
Merino, A ;
Klein, K ;
Hudak, M ;
Dickson, D ;
Rudi, T ;
Gnau, V ;
Bauch, A ;
Bastuck, S ;
Huhse, B ;
Leutwein, C ;
Heurtier, MA ;
Copley, RR ;
Edelmann, A ;
Querfurth, E ;
Rybin, V ;
Drewes, G ;
Raida, M ;
Bouwmeester, T ;
Bork, P ;
Seraphin, B ;
Kuster, B ;
Neubauer, G ;
Superti-Furga, G .
NATURE, 2002, 415 (6868) :141-147
[10]   Structural basis of transcription:: An RNA polymerase II elongation complex at 3.3 Å resolution [J].
Gnatt, AL ;
Cramer, P ;
Fu, JH ;
Bushnell, DA ;
Kornberg, RD .
SCIENCE, 2001, 292 (5523) :1876-1882