Strand-specificity in the transformation of yeast with synthetic oligonucleotides
- PMID: 1325385
- PMCID: PMC1205094
- DOI: 10.1093/genetics/131.4.811
Strand-specificity in the transformation of yeast with synthetic oligonucleotides
Abstract
Cyc1 mutants of the yeast Saccharomyces cerevisiae were directly transformed with both sense and antisense oligonucleotides to examine the involvement of the two genomic DNA strands in transformation. Sense oligonucleotides yielded approximately 20-fold more transformants than antisense oligonucleotides. This differential effect was observed with oligonucleotides designed to make alterations at six different sites along the gene and was independent of the oligonucleotide sequence and length, number of mismatches and the host strain. Competition studies showed that antisense oligonucleotides did not inhibit transformation. Although the mechanism for this strand specificity is unknown, this difference was maintained even when CYC1 transcription was diminished to approximately 2% of the normal level.
Similar articles
-
Parameters affecting the frequencies of transformation and co-transformation with synthetic oligonucleotides in yeast.Yeast. 1992 Nov;8(11):935-48. doi: 10.1002/yea.320081104. Yeast. 1992. PMID: 1336288
-
Transformation of yeast with synthetic oligonucleotides.Proc Natl Acad Sci U S A. 1988 Jan;85(2):524-8. doi: 10.1073/pnas.85.2.524. Proc Natl Acad Sci U S A. 1988. PMID: 2829192 Free PMC article.
-
Synthetic oligodeoxyribonucleotides as tools in molecular genetics: the characterization of the CYC1 (iso-1-cytochrome c encoding) locus of Saccharomyces cerevisiae.Biochimie. 1985 Jul-Aug;67(7-8):717-23. doi: 10.1016/s0300-9084(85)80159-0. Biochimie. 1985. PMID: 3002492
-
Transformation of yeast directly with synthetic oligonucleotides.Methods Enzymol. 1991;194:362-9. doi: 10.1016/0076-6879(91)94027-a. Methods Enzymol. 1991. PMID: 1848647 No abstract available.
-
The importance of mutation, then and now: studies with yeast cytochrome c.Mutat Res. 2005 Jan;589(1):1-16. doi: 10.1016/j.mrrev.2004.07.001. Mutat Res. 2005. PMID: 15652223 Review.
Cited by
-
Oligonucleotide-directed gene repair in wheat using a transient plasmid gene repair assay system.Plant Cell Rep. 2006 May;25(5):457-65. doi: 10.1007/s00299-005-0098-x. Epub 2006 Jan 11. Plant Cell Rep. 2006. PMID: 16404599
-
Genetic spell-checking: gene editing using single-stranded DNA oligonucleotides.Plant Biotechnol J. 2016 Feb;14(2):463-70. doi: 10.1111/pbi.12473. Epub 2015 Sep 24. Plant Biotechnol J. 2016. PMID: 26402400 Free PMC article. Review.
-
Full-length RecE enhances linear-linear homologous recombination and facilitates direct cloning for bioprospecting.Nat Biotechnol. 2012 May;30(5):440-6. doi: 10.1038/nbt.2183. Nat Biotechnol. 2012. PMID: 22544021
-
AAV recombineering with single strand oligonucleotides.PLoS One. 2009 Nov 2;4(11):e7705. doi: 10.1371/journal.pone.0007705. PLoS One. 2009. PMID: 19888330 Free PMC article.
-
Genetic re-engineering of Saccharomyces cerevisiae RAD51 leads to a significant increase in the frequency of gene repair in vivo.Nucleic Acids Res. 2004 Apr 15;32(7):2093-101. doi: 10.1093/nar/gkh506. Print 2004. Nucleic Acids Res. 2004. PMID: 15087488 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous