Species identification by melting analysis of secondary structure of single stranded nucleic acids
Methods of identifying the type of a cell are provided, the methods comprising determining the T m profile of a sample rRNA or fragment thereof from the cell using a double stranded nucleic acid-specific dye, wherein a match between the determined T m profile and the T m profile of a corresponding rRNA or fragment thereof of a cell from a known cell type indicates that the sample rRNA is from the known cell type.
1. A method of identifying the type of a cell, said method comprising:
determining the T m profile of a sample rRNA or fragment thereof from the cell using a double stranded nucleic acid-specific dye by combining said sample rRNA with a double stranded nucleic acid-specific dye to form a detectable complex between said dye and one or more double strand secondary structures within said sample rRNA and measuring fluorescence emission of said double strand nucleic acid-specific dye while varying the temperature of said combination,
wherein a match between said determined T m profile and the T m profile of a corresponding rRNA or fragment thereof of a cell from a known cell type indicates that the sample rRNA is from the known cell type.
2. The method of claim 1 , wherein said temperature is varied at a rate of 0.01°-0.1° C./sec.
3. The methods of claim 1 , wherein the temperature range of said T m profile is between about 20° C. and about 100° C.
4. The method of claim 3 , wherein said lower limit of said temperature range is less than about 40° C.
5. The method of claim 4 , wherein said lower limit of said temperature range is less than about 35° C.
6. The method of claim 1 , wherein a change in fluorescence indicates a change in secondary structure of said sample rRNA.
7. The method of claim 1 , wherein said double stranded nucleic acid-specific dye is selected from the group consisting of SYBR® Green I, SYBR® Gold, ethidium bromide, propidium bromide, Pico Green, Hoechst 33258, YO-PRO-1 and YO-YO-1.
8. The method of claim 1 , wherein the double stranded nucleic acid-specific dye is a saturation dye.
9. The method of claim 1 , wherein said cell is a bacterial cell.
10. The method of claim 1 , wherein said cell is a plant cell.
11. A method of identifying the species type of a cell, said method comprising:
determining the T m profile of an amplified rRNA gene or fragment thereof from the cell using a double stranded nucleic acid-specific dye by combining said amplified rRNA gene or fragment thereof with a double stranded nucleic acid-specific dye to form a detectable complex between said dye and one or more double strand secondary structures within said amplified rRNA gene or fragment thereof and measuring fluorescence emission of said double strand nucleic acid-specific dye while varying the temperature of said combination,
wherein a match between said determined T m profile and the T m profile of a corresponding rRNA gene or fragment thereof of a cell of known species indicates that the rRNA is from the known species.
12. The method of claim 11 , wherein said amplified rRNA gene or fragment thereof is produced by polymerase chain reaction (PCR) amplification.
13. The method of claim 12 , wherein said PCR is asymmetrical PCR.
14. The method of claim 11 , wherein said amplified rRNA gene or fragment thereof is produced by an amplification reaction selected from the group consisting of strand displacement amplification (SDA), rolling circle amplification (RCA), nucleic acid sequence-based amplification (NASBA), transcription mediated amplification (TMA) and ligase chain reaction (LCR).
15. The method of claim 11 , wherein said temperature is varied at a rate of 0.01°-0.1° C./sec.
16. The method of claim 11 , wherein the double strand nucleic acid-specific dye is a saturation dye.
17. The method of claim 16 , wherein the dye is present during amplification of the rRNA gene or fragment thereof
18. The method of claim 16 , wherein the dye has a percent saturation of at least 90%.
19. The method of claim 11 , wherein the amplified rRNA gene or fragment thereof is selected from the group consisting of 5S, 16S, and 23S rRNA genes.