A nomenclature for fungal PCR primers with examples from intron-containing SSU rDNA
- 1 September 1996
- journal article
- research article
- Published by Taylor & Francis in Mycologia
- Vol. 88 (5) , 745-748
- https://doi.org/10.1080/00275514.1996.12026712
Abstract
We present a compilation of polymerase chain reaction primers (oligonucleotides) used to amplify and sequence the small subunit of nuclear ribosomal DNA. To simplify use of these primers we designed a nomenclature that defines the location of each relative to Saccharomyces cerevisiae. With these primers we have developed strategies for selectively amplifying the diverse ribosomal DNA repeat types found in lichens; either between symbionts or between ribosomal DNA repeats (often the product of optional group I introns) within an individual fungus. A diversity of primers allows a choice of which small subunit ribosomal DNA repeat is amplified or sequenced from a complex extract such as that derived from lichens.Keywords
This publication has 7 references indexed in Scilit:
- Multiple Origins of Lichen Symbioses in Fungi Suggested by SSU rDNA PhylogenyScience, 1995
- Small subunit rDNA variation in a population of lichen fungi due to optional group-I intronsGene, 1993
- Numerous group I introns with variable distributions in the ribosomal DNA of a lichen fungusJournal of Molecular Biology, 1992
- Polymerase Chain Reaction (PCR) Primers for Amplifying and Sequencing Nuclear 18s rDNA from Lichenized FungiMycologia, 1992
- Identification of ten additional nucleotides in the primary structure of yeast 18S rRNAGene, 1986
- Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses.Proceedings of the National Academy of Sciences, 1985
- The structure of the yeast ribosomal RNA genes. I. The complete nucleotide sequence of the 18S ribosomal RNA gene from Saccharomyces cerevisiaeNucleic Acids Research, 1980