Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (128K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Mamedov, I.
Right arrow Articles by Sverdlov, E. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mamedov, I.
Right arrow Articles by Sverdlov, E. D.
Related Collections
Right arrow Genomics
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2002, Vol. 30, No. 14 e71
© 2002 Oxford University Press

Genome-wide comparison of differences in the integration sites of interspersed repeats between closely related genomes

Ilgar Mamedov*, Anastasia Batrak, Anton Buzdin, Elena Arzumanyan, Yuri Lebedev and Eugene D. Sverdlov

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya Street, 117997 Moscow, Russia

*To whom correspondence should be addressed. Tel: +7 95 330 69 92; Fax: +7 95 330 65 38; Email: imam{at}humgen.siobc.ras.ru

A technique for genome-wide detection of differences in the integration site positions of interspersed repeats in related genomes (DiffIR) is described. The technique is based on a whole- genome selective PCR amplification of the repeats’ flanking regions followed by a differential hybridization screening of the arrayed library of the selected amplicons. The technique was successfully applied to the comparison of the integration sites in the human and chimpanzee genomes, allowing us to discover 11 new human-specific integrations of human endogenous retrovirus, K family (HML-2) long terminal repeats.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
T. Takabatake, H. Ishihara, Y. Ohmachi, I. Tanaka, M. M. Nakamura, K. Fujikawa, T. Hirouchi, S. Kakinuma, Y. Shimada, Y. Oghiso, et al.
Microarray-based global mapping of integration sites for the retrotransposon, intracisternal A-particle, in the mouse genome
Nucleic Acids Res., June 1, 2008; 36(10): e59 - e59.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
A. Buzdin, E. Kovalskaya-Alexandrova, E. Gogvadze, and E. Sverdlov
At Least 50% of Human-Specific HERV-K (HML-2) Long Terminal Repeats Serve In Vivo as Active Promoters for Host Nonrepetitive DNA Transcription.
J. Virol., November 1, 2006; 80(21): 10752 - 10762.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
I. Z. Mamedov, E. S. Arzumanyan, A. L. Amosova, Y. B. Lebedev, and E. D. Sverdlov
Whole-genome experimental identification of insertion/deletion polymorphisms of interspersed repeats by a new general approach
Nucleic Acids Res., January 26, 2005; 33(2): e16 - e16.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
I. Z. Mamedov, Y. B. Lebedev, and E. D. Sverdlov
Unusually long target site duplications flanking some of the long terminal repeats of human endogenous retrovirus K in the human genome
J. Gen. Virol., June 1, 2004; 85(6): 1485 - 1488.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.