Skip to main content
. Author manuscript; available in PMC: 2012 Mar 1.
Published in final edited form as: Cytoskeleton (Hoboken). 2011 Feb 3;68(3):157–174. doi: 10.1002/cm.20502

Figure 4. GAL1p-PAC1, she1Δ, and num1Δ differentially affect the recruitment of dynein and dynactin to the MT plus end.

Figure 4

Histograms of the number of molecules per plus end focus, shown together with Gaussian fits (see Materials and Methods and Supplementary Note 1), for (A) Dyn1 or Jnm1 in a wild-type (nDyn1 = 380 foci; nJnm1 = 385 foci), GAL1p-PAC1 strain (nDyn1 = 80 foci; nJnm1 = 124 foci), she1Δ (nDyn1 = 100 foci; nJnm1 = 170 foci), or num1Δ (nDyn1 = 52 foci; nJnm1 = 153 foci) strain, or (B) Nip100 in a wild-type or she1Δ strain (nSHE1 = 108 foci; nshe1Δ = 83 foci). Mean values for the first major component (i.e., x̄1 from Fig. S4) ± standard deviation are shown. P values between wild-type and mutant are indicated. For 2-component data sets, only those values probabilistically determined to occupy the first component were used to calculate P values.