A Spindle Checkpoint Functions during Mitosis in the Early Caenorhabditis elegans Embryo
Mol. Biol. Cell Encalada et al.
16: 1056
Supplemental Material
This article contains the following supporting material:
SuppMovie1.mov
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Wild-type embryos lack DNA segregation defects.
Fluorescent spinning disc confocal image of a one-cell wild-type embryo carrying a histone2B and β-tubulin::GFP signal.
SuppMovie2.mov (3.47 MB)
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A one-cell apo-5(or358) embryo without DNA segregation defects.
Fluorescent spinning disc confocal image of a one-cell apo-5(or358) embryo carrying a histone2B and β-tubulin::GFP signal. Notice that during both metaphase and anaphase, chromosomes do not align as tightly as they do in wild-type embryos, perhaps due to incomplete kinetochore-microtuble attachments in apo-5 embryos as compared to wildtype.
SuppMovie3.mov (8.67 MB)
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A one-cell apo-5(or358); mdf-1(RNAi) embryo with severe DNA bridges.
Fluorescent spinning disc confocal image of a one-cell apo-5(or358); mdf-1(RNAi) embryo expressing histone2B::GFP and β-tubulin::GFP fusion proteins. Notice the lack of alignment of chromosomes during presumed metaphase and as the chromosomal masses start to be pulled apart. Severe DNA bridges persist as cytokinesis ensues.