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. 2008 May;20(5):1244–1259. doi: 10.1105/tpc.107.056655

Table 1.

Multiple Clock Outputs Are Disrupted in xct Mutants

Period Estimate (Variance Weighted Mean ± se [n]) in Hours
Genotype DD cRL (40 μE) cBL (20 μE) cR+BL (55 μE) LMRA (20 μE)
Col 25.64 ± 0.36 (6) 25.60 ± 0.07 (35) 24.37 ± 0.09 (17) 24.81 ± 0.08 (16) 24.97 ± 0.17 (31)
xct-1 24.17 ± 0.24 (8) 23.01 ± 0.09 (33) 22.61 ± 0.07 (18) 22.93 ± 0.08 (16) 23.59 ± 0.07 (49)
xct-2 22.71 ± 0.23 (8) 22.47 ± 0.09 (27) 22.52 ± 0.06 (13) 22.27 ± 0.18 (16) 22.23 ± 0.2 (49)
xct-3 25.28 ± 0.44 (7) 25.29 ± 0.08 (33) 24.02 ± 0.13 (16) 24.49 ± 0.12 (16) ND
xct-1 XCTpro:XCT ND 25.28 ± 0.03 (73) ND ND ND
xct-2 XCTpro:XCT ND 25.16 ± 0.11 (18) ND ND ND
xct-2 35Spro:XCT ND 24.92 ± 0.24 (15) ND ND ND

Intensities of constant light conditions are presented in μE (μmol m−2 s−1). CCR2pro:LUC activity was determined in constant darkness (DD), constant red light (cRL), constant blue light (cBL), or the combination of constant red and blue light (cR+BL). Cotyledon movement rhythms (LMRA) were monitored in constant white light. xct mutants transformed with a genomic copy of XCT under the control of the native XCT promoter (XCTpro:XCT) or the globally expressed cauliflower mosaic virus 35S promoter (35Spro:XCT) were assayed in the T1 generation, with similar rescued periods observed in resulting T2 and T3 families. ND represents data not determined; se is the standard error for (n) individuals.