Table 1.
Mutant Number | Mutations(human/yeast equivalents) | Vps35 binding in two- hybrid assay a | Assembly with Vps35, Vps29 in vivo b | Endosomal localization in cells | Rescue of CPY processing in VPS26Δ yeast d | Rescue of CPY secretion in VPS26Δ yeast e |
---|---|---|---|---|---|---|
– | WT | ++ | + | + | + | + |
1 | L431A V144D K145D | ++ | ||||
2 | E13A D15A | ++ | ||||
3 | K133D T135D V137D | ++ | ||||
4 | R69A E71A | ++ | + | + | ||
5 | L97D | ++ | ||||
6 | R127E R129E F131E | ++ | ||||
7 | F79D | ++ | ||||
8 | R271E F273E | ++ | ||||
9 | K214E I216E | ++ | ||||
10 | T225D T227D | ++ | ||||
11 | I230D Y233D | ++ | ||||
12 | L250D F251D | ++ | ||||
13 | F197D L198D | ++ | ||||
14 | V200D I204D | ++ | ||||
15 | I246D | ++ | ||||
16 | I235D M236D/I318D M319D | – | – | – | – | – |
17 | R284E R285E F287E | ++ | ||||
18 | Δ238–246 GG/Δ321–328 GG | – | – | – | – | – |
19 | V190D V192D K194D | ++ | ||||
20 | E177A E179A K182D | ++ | ||||
21 | E165D K167A | ++ | ||||
22 | E171A D172A | ++ | ||||
23 | E281A E182A D183A R284A | ++ | ||||
24 | S49A K51D N53A | ++ | ||||
25 | V137D R139D L140D | ++ | ||||
26 | T102D Q103D R105D | ++ | ||||
27 | D108A E110A M112D | ++ | ||||
28 | V53A A55D K57D | ++ | ||||
29 | K61A R62D E64D | ++ | ||||
30 | E234A D237A | ++ | ||||
31 | I235D | + | ||||
32 | M236D | + | ||||
33 | G238P/G321P | ± | – | – | – | – |
34 | 238–246 polyS/321–328 polyS | ± | – | – | – | – |
35 | Y121F/Y150F | + | + | |||
36 | N125R/N155D | + | + | |||
37 | E215R/E298R | + | + | |||
38 | R296E/R377E | + | + |
Yeast two-hybrid assays were performed as in Fig. 5; ++, normal growth; +, reduced growth in the presence of 10mM 3-AT; ±, lack of growth in the presence of 10mM 3-AT, -, no growth.
Co-precipitation of Vps35 and Vps29 with wild-type or mutant Vps26-myc expressed by transfection in HeLa cells was performed as in Fig. 6; +, normal assembly; -, reduced or no assembly.
Co-localization (+) or lack thereof (−) of wild-type or mutant Vps26-myc with SNX1 on endosomes in HeLa cells analyzed as in Fig. 6. For each condition, 50–75 cells from three independent experiments were examined.
CPY processing and secretion were analyzed as in Fig. 7; for both assays, +, normal function; –, reduced function.