کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5513621 1541218 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The DNA fibre technique - tracking helicases at work
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
The DNA fibre technique - tracking helicases at work
چکیده انگلیسی


- Detailed description of the DNA fibre technique and overview of different experimental setups.
- The DNA fibre technique allows for qualitative and quantitative in vivo analysis of the DNA replication programme.
- Useful assay to analyse helicase function in DNA replication and maintenance of genome stability at a single molecule level.

Faithful duplication of genetic material during every cell division is essential to ensure accurate transmission of genetic information to daughter cells. DNA helicases play a crucial role in promoting this process by facilitating almost all transactions occurring on DNA, including DNA replication and repair. They are responsible not only for DNA double helix unwinding ahead of progressing replication forks but also for resolution of secondary structures like G4 quadruplexes, HJ branch migration, double HJ dissolution, protein displacement, strand annealing and many more. Their importance in maintaining genome stability is underscored by the fact that many human disorders, including cancer, are associated with mutations in helicase genes. Here we outline how DNA fibre fluorography, a straightforward and inexpensive approach, can be employed to study the in vivo function of helicases in DNA replication and the maintenance of genome stability at a single molecule level. This approach directly visualizes the progression of individual replication forks within living cells and hence provides quantitative information on various aspects of DNA synthesis, such as replication fork processivity (replication speed), fork stalling, origin usage and fork termination.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Methods - Volume 108, 1 October 2016, Pages 92-98
نویسندگان
, , ,