Table 2.
Overview of the RNAi dataset for M. abdita
|
hb
RNAi |
gt
RNAi |
Kr
RNAi |
kni
RNAi |
tll
RNAi |
hkb
RNAi |
tll:hkb
RNAi |
|
|---|---|---|---|---|---|---|---|
| hb | n/a | 17/28 (60%) | 21/41 (51%) | 35/52 (67%) | 12/29 (41%) | 21/22 (95%) | 15/15 (100%) |
| gt | 28/35 (80%) | n/a | 13/20 (65%) | 24/30 (80%) | 24/30 (80%) | 10/10 (100%) | 35/36 (97%) |
| Kr | 24/53 (46%) | 7/17 (41%) | n/a | 26/40 (65%) | 7/18 (38%) | 10/10 (100%) | 12/21 (57%) |
| kni | 9/14 (64%) | 11/25 (44%) | 3/21 (14%) | n/a | 6/44 (14%) | 4/10 (40%) | 16/16 (100%) |
| Total | 102 | 70 | 82 | 122 | 121 | 52 | 88 |
A total of 637 RNAi-treated embryos were used for the analysis. This table shows the number of embryos that were stained for each of the trunk gap genes (rows), in each RNAi-treated background (columns), and the number of embryos that showed a knock-down phenotype (see also percentages). The total number of embryos used for each knock-down experiment is shown in the bottom row. A more detailed breakdown of embryos per cleavage cycle and time class, including detailed plots of boundary positions, is provided in Supplementary file 4.