This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zorin, B.
Right arrow Articles by Sizova, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zorin, B.
Right arrow Articles by Sizova, I.

 Previous Article  |  Next Article 

Eukaryotic Cell, July 2005, p. 1264-1272, Vol. 4, No. 7
1535-9778/05/$08.00+0     doi:10.1128/EC.4.7.1264-1272.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Nuclear-Gene Targeting by Using Single-Stranded DNA Avoids Illegitimate DNA Integration in Chlamydomonas reinhardtii{dagger}

Boris Zorin,{ddagger} Peter Hegemann, and Irina Sizova§*

Institut für Biologie, Experimentelle Biophysik, Humboldt-Universität zu Berlin, Invalidenstr.42, 10115 Berlin, Germany

Received 26 March 2005/ Accepted 3 May 2005

Homologous DNA recombination (HR) allows the deletion (knockout), repair (rescuing), and modification of a selected gene, thereby rendering a functional analysis of the gene product possible. However, targeting of nuclear genes has been an inefficient process in most eukaryotes, including algae, plants, and animals, due to the dominance of integration of the applied DNA into nonhomologous regions of the genome. We have shown for the green alga Chlamydomonas reinhardtii by repairing a previously introduced truncated aminoglycoside 3'-phosphotransferase gene, aphVIII, that single-stranded DNA can recombine with a homologous endogenous DNA region of interest. Nonhomologous DNA integration appeared to be more than 100-fold reduced compared with the use of double-stranded DNA, thus allowing isolation of the homologous recombinants. We propose that this method will be applicable to direct targeting of nuclear C. reinhardtii genes.


* Corresponding author. Mailing address: Institut für Biologie, Experimentelle Biophysik, Humboldt-Universität zu Berlin, Invalidenstr. 42, 10115 Berlin, Germany. Phone: 49 30 2093 8830. Fax: 49 30 2093 8585. E-mail: irinasiz{at}yahoo.com.

{dagger} This publication is dedicated to Karen Kindle, who convinced P.H. in 1994 that nuclear-gene targeting is possible in Chlamydomonas.

{ddagger} Present address: Division of Molecular and Radiation Biophysics, Petersburg Nuclear Physics Institute, Russian Academy of Sciences, Gatchina/St. Petersburg, 188350 Russia.

§ Present address: Biological Institute, St. Petersburg State University, Oranienbaumskoye sch, 2, St. Petersburg 198904, Russia.


Eukaryotic Cell, July 2005, p. 1264-1272, Vol. 4, No. 7
1535-9778/05/$08.00+0     doi:10.1128/EC.4.7.1264-1272.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Yang, C., Owen, H. A., Yang, P. (2008). Dimeric heat shock protein 40 binds radial spokes for generating coupled power strokes and recovery strokes of 9 + 2 flagella. JCB 180: 403-415 [Abstract] [Full Text]  
  • Glanz, S., Bunse, A., Wimbert, A., Balczun, C., Kuck, U. (2006). A nucleosome assembly protein-like polypeptide binds to chloroplast group II intron RNA in Chlamydomonas reinhardtii. Nucleic Acids Res 34: 5337-5351 [Abstract] [Full Text]