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. 2014 Apr 15;26(4):1612–1628. doi: 10.1105/tpc.113.120576

Table 3. H2A.Z Deposition at DMC1 Requires ARP6.

Gene ChIP-qPCR Measurement of H2A.Z Enrichment
Fold Difference in H2A.Z Enrichment (WT/arp6-1) P Value
WT
arp6-1
LSM sd LSM sd
DMC1
1 1.89e 0.59 1.76ab 0.88 1.07 0.377
2 1.19f 0.25 1.02d 0.13 1.17 0.033
3 1.31f 0.44 1.56bc 0.41 0.84 0.036
4 1.14f 0.44 0.80def 0.42 1.43 0.041
5 1.42f 0.59 1.39c 0.62 1.02 0.898
6 0.78g 0.30 0.72ef 0.41 1.08 0.550
7 2.48d 0.86 0.99d 0.56 2.51 <0.001
8 3.41b 1.41 0.97de 0.21 3.52 <0.001
9 3.97a 1.88 1.88a 1.36 2.11 <0.001
FLC
A 3.00c 2.04 0.64f 0.67 4.69 <0.001

Numbers in the first column refer to DMC1 genomic region assayed by quantitative PCR for H2A.Z enrichment (as shown in Supplemental Figures 8 and 9). “A” is the genomic region immediately downstream of the transcription start site assayed by quantitative PCR for H2A.Z enrichment in FLC. Least-squares mean (LSM) of H2A.Z enrichment in eight technical replicates (four biological replicates). Within a genotype, any pair of least-squares means that do not share the same letter are significantly different (P ≤ 0.05) from each other in pairwise comparisons for H2A.Z enrichment. The final column is the probability value associated with a pairwise test between LSMs of H2A.Z enrichment at each locus between wild-type (WT) and arp6-1 floral buds. P values ≤ 0.05 indicate significant differences between genotypes.