Abstract
To understand the mechanism and biological effect of viral or foreign DNA insertions, characterization of DNA sequences which contain the integrant-host junction (IHJ) becomes important. The PCR-based strategy to amplify unknown DNA sequences that flank a known integrant has the advantage of simplicity and alacrity. In general, PCR requires a pair of primers both of which are constructed from a known sequence. This is, however, not applicable to study the integration site of a virus or transposable element since only the DNA sequence of the integrant will be known in advance. To circumvent this problem, a variety of PCR-based techniques have been developed. We attempt in this chapter to summarize these methods and discuss the limitation of each.
| Original language | English |
|---|---|
| Title of host publication | PCR Technology |
| Subtitle of host publication | Current Innovations, Second Edition |
| Publisher | CRC Press |
| Pages | 313-322 |
| Number of pages | 10 |
| ISBN (Electronic) | 9781420040654 |
| ISBN (Print) | 9780849311840 |
| State | Published - 01 01 2003 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2004 by CRC Press LLC.