Candidate DNA replication initiation regions at human trinucleotide repeat disease loci

被引:28
作者
Nenguke, T
Aladjem, MI
Gusella, JF
Wexler, NS
Arnheim, N [1 ]
机构
[1] Univ So Calif, Program Mol & Computat Biol, Los Angeles, CA 90089 USA
[2] NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA
[3] Massachusetts Gen Hosp, Dept Psychiat, Mol Neurogenet Unit, Charlestown, MA 02129 USA
[4] Columbia Univ Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[5] Hereditary Dis Fdn, New York, NY 10032 USA
关键词
D O I
10.1093/hmg/ddg111
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
The positions of DNA replication initiation regions (IRs) at three human trinucleotide repeat (TNR) disease loci were examined in order to characterize the role played by IRs in explaining the known locus-specific variation in TNR instability levels. Using three different normal cell lines, candidate IRs were identified at the HD, SCA-7 and SBMA loci. At each locus the IR is less than 3.6 kb from the CAG/CTG repeat tract. Preliminary studies with a cell line homozygous for an HD disease mutation indicated no change in the position of the candidate IR in spite of the mutation. Comparison with experimental results from model systems suggests that a complex relationship may exist between instability and the proximity and/or orientation of the repeats with respect to an IR.
引用
收藏
页码:1021 / 1028
页数:8
相关论文
共 50 条
[1]   Start sites of bidirectional DNA synthesis at the human lamin B2 origin [J].
Abdurashidova, G ;
Deganuto, M ;
Klima, R ;
Riva, S ;
Biamonti, G ;
Giacca, M ;
Falaschi, A .
SCIENCE, 2000, 287 (5460) :2023-2026
[2]   Replication initiation patterns in the β-globin loci of totipotent and differentiated murine cells:: Evidence for multiple initiation regions [J].
Aladjem, MI ;
Rodewald, LW ;
Lin, CM ;
Bowman, S ;
Cimbora, DA ;
Brody, LL ;
Epner, EM ;
Groudine, M ;
Wahl, GM .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (02) :442-452
[3]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[4]   CpG islands as genomic footprints of promoters that are associated with replication origins [J].
Antequera, F ;
Bird, A .
CURRENT BIOLOGY, 1999, 9 (17) :R661-R667
[5]   Identification of initiation sites for DNA replication in the human dnmt1 (DNA-methyltransferase) locus [J].
Araujo, FD ;
Knox, JD ;
Ramchandani, S ;
Pelletier, R ;
Bigey, P ;
Price, G ;
Szyf, M ;
Zannis-Hadjopoulos, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (14) :9335-9341
[6]   Trinucleotide repeat expansion and human disease [J].
Ashley, CT ;
Warren, ST .
ANNUAL REVIEW OF GENETICS, 1995, 29 :703-728
[7]   Methylation-induced repression - Belts, braces, and chromatin [J].
Bird, AP ;
Wolffe, AP .
CELL, 1999, 99 (05) :451-454
[8]  
Bogan JA, 2000, J CELL PHYSIOL, V184, P139, DOI 10.1002/1097-4652(200008)184:2<139::AID-JCP1>3.0.CO
[9]  
2-8
[10]   Cis-acting modifiers of expanded CAG CTG triplet repeat expandability:: associations with flanking GC content and proximity to CpG islands [J].
Brock, GJR ;
Anderson, NH ;
Monckton, DG .
HUMAN MOLECULAR GENETICS, 1999, 8 (06) :1061-1067