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. 2008 May 23;7(7):1211–1221. doi: 10.1128/EC.00272-07

TABLE 3.

Expression assays of putative pheromone precursors (ppg1 and ppg2) and receptors (pre1 and pre2) in different cell types of different ages on carrot agar

Sample ppg1a ppg2 pre1 pre2
3 DAIb (without inductionc)
    Mycelia d
    Ungerminated conidia +
6 DAI (3 days after induction)
    Mycelia ++
    Ungerminated conidia ++
    Germinating conidia ++++ ++
    Young perithecia +++
13 DAI (10 days after induction)
    Mycelia ++
    Ungerminated conidia ++
    Germinating conidia ++++ ++
    Mature perithecia ++
    Ascospores in perithecia +
    Ascospores discharged from perithecia +++ + +
Old culture without induction (15 DAI)
    Mycelia + ++
    Ungerminated conidia + ++
    Germinating conidia ++++ ++
    Mature perithecia ++
    Ascospores in perithecia +
    Ascospores discharged from perithecia +++ + +
a

ppg1, ppg2, pre1, and pre2 expression was assayed with GFP reporter constructs Δppg1GFPR, Δppg2GFPR, Δpre1GFPR, and Δpre2GFPR, respectively.

b

DAI, days after inoculation.

c

Induction by knockdown of mycelia with 500 μl of 2.5% Tween 60 solution to induce sexual development.

d

−, GFP fluorescence signal not detected; +, weak fluorescence; ++, moderate fluorescence; +++, strong fluorescence; ++++, very strong fluorescence; NT, not tested.