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. 2012 Aug 28;160(3):1357–1372. doi: 10.1104/pp.112.203083

Table I. Inflorescence transcriptome changes are similar to those in developing stamen/pollen, in developmentally senescing leaves, and in tissues whose carbohydrate status is altered.

The 758 up-regulated and 741 down-regulated genes were compared with data sets from hundreds of transcriptome studies using Genevestigator V3. The data sets whose transcript profiles most closely matched the changes in the detached dark-held inflorescences are shown. The pollen set was derived from gene transcripts whose accumulation in pollen was 2-fold or more greater than in mature leaf tissue and that showed less than 2-fold change in response to carbohydrate- or senescence-related signaling. Ext, Leaves of whole rosettes held for extended periods (as indicated) in the dark; Sen, developmentally senescing leaves; Glc, seedlings grown in liquid medium containing 0.5% Glc for 7 d, then in medium lacking Glc for 24 h, and then in medium containing 3% Glc for 4 h; CO2, intact rosette leaves illuminated at the end of night for 4 h at 50 µL L−1 versus 350 µL L−1 [CO2]; Light, intact rosette leaves held at 50 µL L−1 [CO2] in light versus 50 µL L−1 [CO2] in dark for 4 h at the end of the night. The percentage of inflorescence genes showing similarity in transcript accumulation with each specified data set is given in parentheses. Percentages for the up-regulated genes were calculated from the set of 553 non-pollen-associated genes, except for the pollen-associated genes (calculated from 758 genes).

Regulation Pollen Ext Early (2 and 4 h) Ext Mid (6 and 8 h) Ext Late (24 and 48 h) Sen Glc CO2 Light
Up-regulated 205 (27) 191 (35) 305 (55) 380 (69) 205 (37) 313 (57) 329 (59) 31(6)
Down-regulated 78 (11) 327 (44) 464 (63) 422 (57) 206 (28) 282 (38) 54(7)