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. 2008 May 5;28(13):4261–4274. doi: 10.1128/MCB.02252-07

TABLE 1.

Characteristics of the GTPases selected for the first screen and their effect on pckb-2::gfp reporter activationa

Phenotype WormBase IDb Designation Subcellular localizationc Functions related to the ER (reference)
No effect C44C11.1 RAS-1 Endomembrane (ER/G) Intracellular protein transport, ER signal transduction (33)
F53G12.1 RAB-11.1 TGN recycling/exocytic compartment Membrane fusion, vesicular trafficking
F54C9.10 ARL-1 TGN/G Membrane fusion and traffic
F53F10.4 UNC-108 ER/cis-G Endocytosis, membrane fusion, vesicular trafficking
W01H2.3 RAB-37 Secretory granules Vesicle exocytosis
ZK792.6 LET-60 Endomembrane (ER/G) Intracellular protein transport, ER signal transduction (33)
C27B7.8 RAP-1 G Membrane fusion, vesicular trafficking
F45E4.1 ARF-1.1 G/ERGIC/TGN Mitotic Golgi fragmentation, vesicular trafficking
Severe developmental defects C39F7.4 RAB-1 ER/cis-G Intracellular vesicle trafficking
W03C9.3 RAB-7 ER/LE/endosome Endosomal traffic, vesicular trafficking
Induction of basal ER stress ZK180.4 SAR-1 ER ER-to-Golgi protein transport
ER stress inhibition R07G3.1 CDC-42 ER/G Cell polarity, protein trafficking
Y32F6B.3 CRP-1 TGN/RE Membrane trafficking, cell polarity (19)
a

pckb-2::gfp reporter worms were treated with selected GTPase RNAi vectors and exposed or not to TM for 5 hours. The consequence of GTPase silencing on the activation of ckb-2 promoters was measured using a fluorescence microscope, and GTPases were classified according to their effect on this reporter into four categories.

b

ID, identification.

c

G, Golgi apparatus; TGN, trans-Golgi network; ERGIC, ER-Golgi intermediate compartment; LE, late endosomes; RE, recycling endosomes.