2014 年 55 巻 6 号 p. 425-430
A novel application for reverse transcription loop-mediated isothermal amplification (reverse transcription LAMP) was developed which enables rapid, accurate and inexpensive detection of gene expression in pure culture mycelia with no previous mRNA isolation necessary as well as in infected plant tissue after mRNA isolation. Usefulness of the method was demonstrated by detection of mRNA templates of the Fusarium graminearum housekeeping genes coding for Ef1α and β-tubulin, in mycelia and in planta.