Table III.

Mitotic stability upon depletion of Chl4p


Relevant genotype

Colonies (%)a

No. of colonies scoredb

nb

% Stabilityc (+URA)

 
Red
 
Red + white sectored
 
White
 

 

 

 
WT 16.0 67.0 17.0 980 89 ± 2.0 
chl4Δ <0.5 19.0 81.0 1,397 10 ± 2.0 
GALUBICHL4       
Galactose 2.0 75.0 23.0 415 80 ± 3.0 
Glucose <0.5 13.0 86.0 2,019 9 ± 3.0 
Gal→Glu
 
1.0
 
75.0
 
24.0
 
3,287
 
10
 
59 ± 14.0
 

Relevant genotype

Colonies (%)a

No. of colonies scoredb

nb

% Stabilityc (+URA)

 
Red
 
Red + white sectored
 
White
 

 

 

 
WT 16.0 67.0 17.0 980 89 ± 2.0 
chl4Δ <0.5 19.0 81.0 1,397 10 ± 2.0 
GALUBICHL4       
Galactose 2.0 75.0 23.0 415 80 ± 3.0 
Glucose <0.5 13.0 86.0 2,019 9 ± 3.0 
Gal→Glu
 
1.0
 
75.0
 
24.0
 
3,287
 
10
 
59 ± 14.0
 
a

Colonies were scored as being red, white, or colonies with red and white sectors after 3 d and expressed as a percent of the total number of colonies scored.

b

Number of colonies scored is the sum of the number of red, white, or red and white–sectored colonies for each transformant analyzed. n, number of independent transformants assayed.

c

Expressed as colonies that were URA/colonies on YPD or YPG. For % stability of gal→glu, cells grown overnight in galactose were switched to YPD media for 8–10 h before plating on YPD.

pDLB2064 was transformed into the GAL1UBICHL4 strain on glucose and galactose and selected on either Glu-uracil or Gal-uracil. Single colonies were grown on YPD/YPG overnight and plated on YPD/YPG plates. For the gal→glu transitions, single colonies from galactose transformants were grown on gal-uracil media overnight at 30°C. Cells were washed and shifted to YPD media for 8–10 h and plated onto YPD plates.

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