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. Author manuscript; available in PMC: 2009 Oct 1.
Published in final edited form as: Dev Cell. 2008 Oct;15(4):603–616. doi: 10.1016/j.devcel.2008.08.005

Table 2.

Microinjection of cdc-48.3 dsRNA leads to mitotic defects

Stage* >2 Centrosomes Unattached chromosomes Chromosome congression defects Chromosome segregation defects
Prophase
control(RNAi)
(n=11)
0.00% 0.00% 0.00% N/A
cdc-48.3(RNAi)
(n=13)
15.38% 7.69% 30.77% N/A
Prometaphase
control(RNAi)
(n=14)
0.00% 0.00% 0.00% N/A
cdc-48.3(RNAi)
(n=10)
20.00% 10.00% 30.00% N/A
Metaphase
control(RNAi)
(n=7)
0.00% 0.00% 0.00% N/A
cdc-48.3(RNAi)
(n=7)
14.29% 28.57% 57.14% N/A
Anaphase
control(RNAi)
(n=26)
0.00% 0.00% N/A 0.00%
cdc-48.3(RNAi)
(n=22)
22.73% 9.09% N/A 45.45%
Telophase
control(RNAi)
(n=16)
0.00% 0.00% N/A 0.00%
cdc-48.3(RNAi)
(n=17)
11.76% 17.65% N/A 41.18%
Late Telophase/G1
control(RNAi)
(n=24)
0.00% 0.00% N/A 0.00%
cdc-48.3(RNAi)
(n=23)
26.09% 17.39% N/A 56.52%
*

Embryos from mock and cdc-48.3 dsRNA microinjected L4 hermaphrodites were fixed and stained with DAPI and α-tubulin antibodies. Mitotic defects in one-cell embryos at various mitotic stages were tabulated. Similar defects were also present in older embryos.