Skip to main content
. 2001 Sep 1;29(17):3459–3468. doi: 10.1093/nar/29.17.3459

Table 2. Survey of differential screening experiments in nodulation research.

Host plant
Technique
Sourcea
Screenedb
Candidatesc
Processedd
Confirmede
Newf
Ref
Pea DH –; wt 14 d 600 6 6 6 91
Soybean DH –; wt 10 d 10 10 3 >1 92
Pea DH –; wt 2 d 3000 3 3 106
Soybean SH –; wt 21 d 150 000 1200 20 9 93
    –; wt 8 d 100 000 250        
Broad bean SH –; wt 30 d 55 000 700 700 27 19 104
Alfalfa DH –; spontaneous nod. 1 107
Pea SH –; wt 35 d 60 000 500 500 19 108
M.truncatula SH –; wt 48, 108 h 1 109
S.rostrata DD –; wt 2, 3, 4 d 2800 45 17 5 5 82
M.truncatula SH nodA; wt 4 d 30 000 473 473 30 29 110
Vetch DD –; NF 1, 3 h 27 600 34 9 1 1 100
L.japonicus DD –; wt 7, 11, 13, 21 d 8000 137 137 19 13 101
M.truncatula ESTS root hair-enriched root 985 899 97
M.truncatula DD –; NF 2 h 4000 0 111
    –; NF 24 h 2400 0 111
    –; NF 48 h 2000 4 4 2 >1 111
Alfalfa CPS –; spontaneous nod. 250 21 21 14 14 95
M.truncatula ESTS wt 4–8 d 408 389 389 117 84 98
Alfalfa CPS Nod; wt 5 d 1000 38 38 38 22 96
Yellow lupine DD –; wt 21 d 3500 50 14 4 4 112
S.rostrata DD –; wt 1, 2, 4, 8, 12, 48 h 4000 57 34 9 6 this work

DH, differential hybridization; SH, subtractive hybridization; DD, differential display; ESTS, EST sequencing; CPS, cold-plaque screening.

aSamples compared in the experiment: –, uninoculated; wt, wild-type microsymbiont; nodA and Nod, mutant microsymbiont strains; NF, pure Nod factors. For details, see original articles.

bNumber of clones screened as plaques or colonies in the case of differential or subtractive hybridization and cold-plaque screening, bands displayed on gel for differential display, or corresponding to the number of clones sequenced in the case of EST sequencing. For the reports on differential display experiments in which no average amount of bands displayed per gel was cited, 100 was taken as the amount to calculate the approximate number of bands visualized.

cNumber of candidates, putatively differentially expressed, obtained in the differential screening experiment, or the number of readable sequences from EST sequencing.

dNumber of candidates that were further processed to confirm their differential expression pattern.

eNumber of unique clones for which the differential expression pattern could be confirmed.

fNumber of novel genes among the confirmed clones.