Combing the genome for genomic instability

作者: Aaron Bensimon , Sandrine Caburet , Chiara Conti

DOI: 10.1016/S0167-7799(02)01990-X

关键词:

摘要: Genomic instability is one of the major features cancer cells. The clinical phenotypes associated with several human diseases have been linked to recurrent DNA rearrangements and dysfunction replication processes that involve unstable genomic regions. Analysis these rearrangements, which are frequently submicroscopic can lead loss or gain dosage-sensitive genes gene disruption, requires development sensitive, high-resolution techniques. This will a better understanding mechanisms underlying genome greater awareness role chromosomal in disease. A new technology involves molecular combing, method permits straightening aligning molecules DNA, should make possible detailed analysis events at level single molecules. Such molecule approach could help elucidate important properties masked bulk studies.

参考文章(66)
John Herrick, Aaron Bensimon, Imaging of single DNA molecule: applications to high-resolution genomic studies. Chromosome Research. ,vol. 7, pp. 409- 423 ,(1999) , 10.1023/A:1009276210892
R Karhu, A Palotie, E Hellsten, O P Kallioniemi, L Peltonen, M Heiskanen, High resolution mapping using fluorescence in situ hybridization to extended DNA fibers prepared from agarose-embedded cells. BioTechniques. ,vol. 17, pp. 928- 933 ,(1994)
J. Julian Blow, Eukaryotic DNA replication IRL Press at Oxford University Press. ,(1996)
Daniel Pinkel, Richard Segraves, Damir Sudar, Steven Clark, Ian Poole, David Kowbel, Colin Collins, Wen-Lin Kuo, Chira Chen, Ye Zhai, Shanaz H. Dairkee, Britt-marie Ljung, Joe W. Gray, Donna G. Albertson, High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays Nature Genetics. ,vol. 20, pp. 207- 211 ,(1998) , 10.1038/2524
Donna G. Albertson, Bauke Ylstra, Richard Segraves, Colin Collins, Shanaz H. Dairkee, David Kowbel, Wen-Lin Kuo, Joe W. Gray, Daniel Pinkel, Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene. Nature Genetics. ,vol. 25, pp. 144- 146 ,(2000) , 10.1038/75985
Kum Kum Khanna, Stephen P. Jackson, DNA double-strand breaks: signaling, repair and the cancer connection. Nature Genetics. ,vol. 27, pp. 247- 254 ,(2001) , 10.1038/85798
Georgia Bardi, Georgia Bardi, Nikos Pandis, Nikos Pandis, Manuel R. Teixeira, Johan A. Andersen, Severre Heim, Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer Cancer Research. ,vol. 56, pp. 855- 859 ,(1996)
Terry L. Orr-Weaver, Robert A. Weinberg, A checkpoint on the road to cancer Nature. ,vol. 392, pp. 223- 224 ,(1998) , 10.1038/32520
Narayana Battula, Lawrence A. Loeb, Clark F. Springgate, Errors in DNA Replication as a Basis of Malignant Changes Cancer Research. ,vol. 34, pp. 2311- 2321 ,(1974)
Susan Margaret Gasser, Christian Frei, RecQ-like helicases: the DNA replication checkpoint connection. Journal of Cell Science. ,vol. 113, pp. 2641- 2646 ,(2000)