Unique condensation patterns of triplex DNA: physical aspects and physiological implications

被引:27
作者
Goobes, R [1 ]
Cohen, O [1 ]
Minsky, A [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
基金
以色列科学基金会;
关键词
D O I
10.1093/nar/30.10.2154
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
Triple-stranded DNA structures can be formed in living cells, either by native DNA sequences or following the application of antigene strategies, in which triplex-forming oligonucleotides are targeted to the nucleus. Recent studies imply that triplex motifs may play a role in DNA transcription, recombination and condensation processes in vivo. Here we show that very short triple-stranded DNA motifs, but not double-stranded segments of a comparable length, self-assemble into highly condensed and ordered structures. The condensation process, studied by circular dichroism and polarized-light microscopy, occurs under conditions that mimic cellular environments in terms of ionic strength, ionic composition and crowding. We argue that the unique tendency of triplex DNA structures to self-assemble, a priori unexpected in light of the very short length and the large charge density of these motifs, reflects the presence of strong attractive interactions that result from enhanced ion correlations. The results provide, as such, a direct experimental link between charge density, attractive interactions between like-charge polymers and DNA packaging. Moreover, the observations strongly support the notion that triple-stranded DNA motifs may be involved in the regulation of chromosome organization in living cells.
引用
收藏
页码:2154 / 2161
页数:8
相关论文
共 61 条
[1]   Triplex DNA in the nucleus: Direct binding of triplex-specific antibodies and their effect on transcription, replication and cell growth [J].
Agazie, YM ;
Burkholder, GD ;
Lee, JS .
BIOCHEMICAL JOURNAL, 1996, 316 :461-466
[2]   Understanding oligonucleotide-mediated inhibition of gene expression in Xenopus laevis oocytes [J].
Bailey, C ;
Weeks, DL .
NUCLEIC ACIDS RESEARCH, 2000, 28 (05) :1154-1161
[3]   Unambiguous demonstration of triple-helix-directed gene modification [J].
Barre, FX ;
Ait-Si-Ali, S ;
Giovannangeli, C ;
Luis, R ;
Robin, P ;
Pritchard, LL ;
Hélène, C ;
Harel-Bellan, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3084-3088
[4]   CONDENSATION OF DNA BY MULTIVALENT CATIONS - CONSIDERATIONS ON MECHANISM [J].
BLOOMFIELD, VA .
BIOPOLYMERS, 1991, 31 (13) :1471-1481
[5]   DNA condensation [J].
Bloomfield, VA .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1996, 6 (03) :334-341
[6]   DNA triple-helix formation on nucleosome-bound poly(dA)•poly(dT) tracts [J].
Brown, PM ;
Fox, KR .
BIOCHEMICAL JOURNAL, 1998, 333 :259-267
[7]   IMMUNOFLUORESCENT LOCALIZATION OF TRIPLEX DNA IN POLYTENE CHROMOSOMES OF CHIRONOMUS AND DROSOPHILA [J].
BURKHOLDER, GD ;
LATIMER, LJP ;
LEE, JS .
CHROMOSOMA, 1991, 101 (01) :11-18
[8]   Inhibition of gene expression and cell proliferation by triple helix-forming oligonucleotides directed to the c-myc gene [J].
Catapano, CV ;
McGuffie, EM ;
Pacheco, D ;
Carbone, GMR .
BIOCHEMISTRY, 2000, 39 (17) :5126-5138
[9]   STRUCTURE AND STABILITY OF Z-STAR-DNA [J].
CHAIRES, JB ;
NORCUM, MT .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1988, 5 (06) :1187-1207
[10]   PRECIPITATION OF HIGHLY-CHARGED POLYELECTROLYTE SOLUTIONS IN THE PRESENCE OF MULTIVALENT SALTS [J].
DELACRUZ, MO ;
BELLONI, L ;
DELSANTI, M ;
DALBIEZ, JP ;
SPALLA, O ;
DRIFFORD, M .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (13) :5781-5791