A versatile in vivo footprinting technique using 1,10-phenanthroline-copper complex to study important cellular processes

被引:19
作者
Basak, S
Nagaraja, V [1 ]
机构
[1] Indian Inst Sci, Dept Microbiol & Cell Biol, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Jawaharlal Nehru Ctr Adv Sci Res, Bangalore 560012, Karnataka, India
关键词
D O I
10.1093/nar/29.21.e105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A number of reagents have been used to define the sequence-specific protein-DNA contacts by footprinting analysis. We report a new in vivo technique using the complex of 1,10-phenanthroline and copper [(OP2)Cu] as a probe to study various intracellular DNA-protein interactions in wholecells. The versatility of the protocol is demonstrated by applying the technique to address various processes. The protocol is applied to (i) detect structural alterations in DNA as a result of single base substitution, (ii) footprint site-specific DNA-binding proteins, (iii) analyze promoter occupancy by RNA polymerase and (iv) analyze molecular interactions during transcription initiation. The results demonstrate that in vivo (OP)(2)Cu probing is a useful tool in studying important cellular processes involving DNA-protein interactions and has potential applications in post-genomic research.
引用
收藏
页数:6
相关论文
共 31 条
[1]   FUNCTIONALLY DISTINCT RNA-POLYMERASE BINDING-SITES IN THE PHAGE MU MOM PROMOTER REGION [J].
BALKE, V ;
NAGARAJA, V ;
GINDLESPERGER, T ;
HATTMAN, S .
NUCLEIC ACIDS RESEARCH, 1992, 20 (11) :2777-2784
[2]   Intrinsic DNA distortion of the bacteriophage Mu momP1 promoter is a negative regulator of its transcription -: A novel mode of regulation of toxic gene expression [J].
Basak, S ;
Olsen, L ;
Hattman, S ;
Nagaraja, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :19836-19844
[3]   Inhibition of Mycobacterium smegmatis topoisomerase I by specific oligonucleotides [J].
Bhaduri, T ;
Basak, S ;
Sikder, D ;
Nagaraja, V .
FEBS LETTERS, 2000, 486 (02) :126-130
[4]   HIGH-RESOLUTION ANALYSIS OF LAC TRANSCRIPTION COMPLEXES INSIDE CELLS [J].
BOROWIEC, JA ;
GRALLA, JD .
BIOCHEMISTRY, 1986, 25 (18) :5051-5057
[5]   FACTOR INTERACTIONS AT SIMIAN VIRUS-40 GC-BOX PROMOTER ELEMENTS IN INTACT NUCLEI [J].
BUCHANAN, RL ;
GRALLA, JD .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (04) :1554-1558
[6]   Drunken-cell footprints: nuclease treatment of ethanol-permeabilized bacteria reveals an initiation-like nucleoprotein complex in stationary phase replication origins [J].
Cassler, MR ;
Grimwade, JE ;
McGarry, KC ;
Mott, RT ;
Leonard, AC .
NUCLEIC ACIDS RESEARCH, 1999, 27 (23) :4570-4576
[7]   Characterization of DNA binding activities of over-expressed KpnI restriction endonuclease and modification methylase [J].
Chandrashekaran, S ;
Babu, P ;
Nagaraja, V .
JOURNAL OF BIOSCIENCES, 1999, 24 (03) :269-277
[8]  
GALAZKA G, 1986, J BIOL CHEM, V261, P7093
[9]   IN-VITRO TRANSCRIPTIONAL ACTIVATION OF THE PHAGE-MU MOM PROMOTER BY C-PROTEIN [J].
GINDLESPERGER, TL ;
HATTMAN, S .
JOURNAL OF BACTERIOLOGY, 1994, 176 (10) :2885-2891
[10]   RAPID FOOTPRINTING ON SUPERCOILED DNA [J].
GRALLA, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (10) :3078-3081