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. 2016 Dec 23;12(2):e1274481. doi: 10.1080/15592324.2016.1274481

Table 1.

A summary of G. max candidate gene expression.

    Time point (dpi)
 
Gene Accession 0* 3 6
Sec14-1 Glyma14g08180 N/M N/M M
Sec4-6 Glyma20g23210 N/M N/M M
Sec23-5 Glyma18g00670 N/M M M
Bro1-1 Glyma02g10910 N/M M M
SYP6-1 Glyma17g07100 N/M M M
SYP131-1 Glyma12g32100 N/M M M
SYP71-6 Glyma19g36410 N/M N/M M
SYP8-2 Glyma14g02120 M M M
Bet1-1 Glyma06g10370 M M M
Cε−1 Glyma09g03500 M M M
Cζ−3 Glyma15g01150 M M M
ERGIC-3-3 Glyma13g01920 M M M
RO-40 Glyma15g14040 N/M N/M M
XXT 2-5 Glyma19g39760 N/M N/M M
GS-3 Glyma19g41550 N/M N/M M
AP2-1 Glyma01g44130 N/M N/M N/M

Footnote. Laser microdissection has been used to collect control cells (pericycle) at 0 days post infection (dpi) and Heterodera glycines-induced syncytia undergoing the process of resistance at 3 and 6 dpi. * Uninoculated roots have been used to obtain pericycle cells which have served as the source of the control mRNA samples. M (red) probe has been measured. N/M (blue), probe has not been measured. For details, please see Table S1.