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. 1998 Jun 1;18(11):4063–4075. doi: 10.1523/JNEUROSCI.18-11-04063.1998

Table 2.

The four functional CMTX mutations interact with Cx32wt and retain its same selective compatibility in heterotypic channel formation

Oocyte injection (cell 1/cell 2) Gj (μS) Number of pairs
Antisense/antisense 0.04  ± 0.03 5
L56F/Cx32wt 13.9  ± 3.3 9
E102G/Cx32wt 20.5  ± 6.4 11
Del111–116/Cx32wt 6.0  ± 1.9 10
R220stop/Cx32wt 6.4  ± 2.4 7
L56F/Cx26 9.3  ± 2.5 6
L56F/Cx46 9.6  ± 3.2 4
L56F/Cx50 10.3  ± 3.2 5
E102G/Cx26 5.0  ± 0.9 3
E102G/Cx46 5.7  ± 1.4 4
E102G/Cx50 3.6  ± 1.3 3
Del111–116/Cx26 5.9  ± 0.8 10
Del111–116/Cx46 4.8  ± 1.1 6
Del111–116/Cx50 5.9  ± 1.0 5
R220stop/Cx26 2.1  ± 0.7 5
R220stop/Cx46 3.4  ± 0.9 7
R220stop/Cx50 2.0  ± 0.6 5
L56F/Cx40 0.06  ± 0.04 4
E102G/Cx40 0.03  ± 0.01 6
Del111–116/Cx40 0.01  ± 0.01 4
R220stop/Cx40 0.01  ± 0.01 6

Antisense-treated cells were injected with the specified cRNAs, and measurements of steady-state junctional conductance (Gj) were performed 24–48 hrs after pairing, using a dual voltage-clamp procedure. Whereas the four functional CMTX mutations failed to interact with Cx40, homotypic Cx40/Cx40 pairs injected with the same RNA batch developed a robust junctional conductance (16.0 ± 0.2 μS; n = 3). Results are shown as the mean ± SEM of the number of pairs indicated.