Sticky DNA, a long GAA•GAA•TTC triplex that is formed intramolecularly, in the sequence of intron 1 of the frataxin gene

被引:55
作者
Vetcher, AA
Napierala, M
Iyer, RR
Chastain, PD
Griffith, JD
Wells, RD
机构
[1] Texas A&M Univ, Inst Biosci & Technol, Ctr Genome Res, Med Ctr, Houston, TX 77030 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
关键词
D O I
10.1074/jbc.M205209200
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
Friedreich's ataxia is caused by the massive expansion of GAA.TTC repeats in intron I of the frataxin-(X25) gene. Our prior investigations showed that long GAA.TTC repeats formed very stable triplex structures which caused two repeat tracts to adhere to each other (sticky DNA). This process was dependent on negative supercoiling and the presence of divalent metal ions. Herein, we have investigated the formation of sticky DNA from plasmid monomers and dimers; sticky DNA is formed only when two tracts of sufficiently long (GAA.TTC)(n) (n = 59-270) are present in a single plasmid DNA and are in the direct repeat orientation. If the inserts are in the indirect (inverted) repeat orientation, no sticky DNA was observed. Furthermore, kinetic studies support the intramolecular nature of sticky DNA formation. Electron microscopy investigations also provide strong data for sticky DNA as a single long triplex. Hence, these results give new insights into our understanding of the capacity of sticky DNA to inhibit transcription and thereby reduce the level of frataxin protein as related to the etiology of Friedreich's ataxia.
引用
收藏
页码:39217 / 39227
页数:11
相关论文
共 52 条
[1]  
[Anonymous], 1983, COLD SPRING HARBOR L
[2]   The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure [J].
Bidichandani, SI ;
Ashizawa, T ;
Patel, PI .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (01) :111-121
[3]  
Bidichandani SI, 1997, AM J HUM GENET, V60, P1251
[4]   USE OF SITE-SPECIFIC RECOMBINATION AS A PROBE OF DNA-STRUCTURE AND METABOLISM INVIVO [J].
BLISKA, JB ;
COZZARELLI, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 194 (02) :205-218
[5]   STRUCTURE OF PLECTONEMICALLY SUPERCOILED DNA [J].
BOLES, TC ;
WHITE, JH ;
COZZARELLI, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 213 (04) :931-951
[6]   Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion [J].
Campuzano, V ;
Montermini, L ;
Molto, MD ;
Pianese, L ;
Cossee, M ;
Cavalcanti, F ;
Monros, E ;
Rodius, F ;
Duclos, F ;
Monticelli, A ;
Zara, F ;
Canizares, J ;
Koutnikova, H ;
Bidichandani, SI ;
Gellera, C ;
Brice, A ;
Trouillas, P ;
DeMichele, G ;
Filla, A ;
DeFrutos, R ;
Palau, F ;
Patel, PI ;
DiDonato, S ;
Mandel, JL ;
Cocozza, S ;
Koenig, M ;
Pandolfo, M .
SCIENCE, 1996, 271 (5254) :1423-1427
[7]   Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes [J].
Campuzano, V ;
Montermini, L ;
Lutz, Y ;
Cova, L ;
Hindelang, C ;
Jiralerspong, S ;
Trottier, Y ;
Kish, SJ ;
Faucheux, B ;
Trouillas, P ;
Authier, FJ ;
Durr, A ;
Mandel, JL ;
Vescovi, A ;
Pandolfo, M ;
Koenig, M .
HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1771-1780
[8]   Frataxin fracas [J].
Cossee, M ;
Campuzano, V ;
Koutnikova, H ;
Fischbeck, K ;
Mandel, JL ;
Koenig, M ;
Bidichandani, SI ;
Patel, PI ;
Molte, MD ;
Canizares, J ;
DeFrutos, R ;
Pianese, L ;
Cavalcanti, F ;
Monticelli, A ;
Cocozza, S ;
Montermini, L ;
Pandolfo, M .
NATURE GENETICS, 1997, 15 (04) :337-338
[9]   Clinical and genetic abnormalities in patients with Friedreich's ataxia [J].
Durr, A ;
Cossee, M ;
Agid, Y ;
Campuzano, V ;
Mignard, C ;
Penet, C ;
Mandel, JL ;
Brice, A ;
Koenig, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (16) :1169-1175
[10]  
Filla A, 1996, AM J HUM GENET, V59, P554