Table I.

Parameters of MT growth in CHO-K1 cells

 Number of observations Length of uninterrupted growtha Growth rateb Catastrophe frequencyc 
  μm μm/min min−1 
Expression of shRNA     
Luciferase; YFP-CLIP-170 100 MTs; 7 cells 15.6 ± 8.8 24.3 ± 8.3 0.3 ± 0.1 
Luciferase; Cy3-tubulin 37 MTs; 3 cells 13.4 ± 5.9 18.5 ± 5.3 0.2 ± 0.1 
EB1; YFP-CLIP-170 88 MTs; 7 cells 14.5 ± 6.4 21.4 ± 9.4 0.3 ± 0.1 
EB1/EB3; YFP-CLIP-170 101 MTs; 8 cells 7.3 ± 4.5 22.6 ± 8.4 3.2 ± 0.9 
EB1/EB3; Cy3-tubulin 56 MTs; 3 cells 7.4 ± 4.1 22.4 ± 5.5 3.7 ± 0.7 
Rescue experiments in EB1/EB3-depleted cells     
EB1 rescue; YFP-CLIP-170 64 MTs; 7 cells 15.1 ± 7.0 21.1 ± 8.0 0.3 ± 0.1 
EB1ΔAc rescue; YFP-CLIP-170 96 MTs; 10 cells 16.6 ± 7.3 26.9 ± 10.7 0.3 ± 0.1 
Expression of EB1 mutants     
EB1-NL (control); YFP-CLIP-170 88 MTs; 7 cells 18.5 ± 7.1 22.5 ± 7.1 0.2 ± 0.1 
EB1-CΔAc; YFP-CLIP-170 116 MTs; 9 cells 4.5 ± 2.9 20.3 ± 7.9 4.2 ± 1.0 
EB1-CΔAc; Cy3-tubulin 55 MTs; 4 cells 4.8 ± 3.4 18.7 ± 7.8 3.5 ± 0.9 
 Number of observations Length of uninterrupted growtha Growth rateb Catastrophe frequencyc 
  μm μm/min min−1 
Expression of shRNA     
Luciferase; YFP-CLIP-170 100 MTs; 7 cells 15.6 ± 8.8 24.3 ± 8.3 0.3 ± 0.1 
Luciferase; Cy3-tubulin 37 MTs; 3 cells 13.4 ± 5.9 18.5 ± 5.3 0.2 ± 0.1 
EB1; YFP-CLIP-170 88 MTs; 7 cells 14.5 ± 6.4 21.4 ± 9.4 0.3 ± 0.1 
EB1/EB3; YFP-CLIP-170 101 MTs; 8 cells 7.3 ± 4.5 22.6 ± 8.4 3.2 ± 0.9 
EB1/EB3; Cy3-tubulin 56 MTs; 3 cells 7.4 ± 4.1 22.4 ± 5.5 3.7 ± 0.7 
Rescue experiments in EB1/EB3-depleted cells     
EB1 rescue; YFP-CLIP-170 64 MTs; 7 cells 15.1 ± 7.0 21.1 ± 8.0 0.3 ± 0.1 
EB1ΔAc rescue; YFP-CLIP-170 96 MTs; 10 cells 16.6 ± 7.3 26.9 ± 10.7 0.3 ± 0.1 
Expression of EB1 mutants     
EB1-NL (control); YFP-CLIP-170 88 MTs; 7 cells 18.5 ± 7.1 22.5 ± 7.1 0.2 ± 0.1 
EB1-CΔAc; YFP-CLIP-170 116 MTs; 9 cells 4.5 ± 2.9 20.3 ± 7.9 4.2 ± 1.0 
EB1-CΔAc; Cy3-tubulin 55 MTs; 4 cells 4.8 ± 3.4 18.7 ± 7.8 3.5 ± 0.9 
a

The length of YFP-CLIP-170 or tubulin tracks represents the length of persistent growth.

b

The growth rate ± SD was calculated from the histogram of displacements of YFP-CLIP-170–positive tips or Cy3-labeled MT ends between successive frames.

c

The catastrophe frequency (the number of transition events over time) was calculated for each cell and was presented as an average ± SD for the cell population.

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