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. 2009 Apr 5;388(1):147–159. doi: 10.1016/j.virol.2009.02.049

Table 1.

Determination of interactions among CymMV encoded triple gene block proteins by yeast two-hybrid assay.

AD fusiona BD fusiona Trp− and Leu− mediumb Trp−, Leu−, His− and Ade− mediumc Histochemical assayd (X-α-gal)
T-antigene p53e +++ +++ +++
TGBp1 +++ NA
TGBp2 +++ NA
TGBp3 +++ NA
CP +++ NA
TGBp1 +++ NA
TGBp2 +++ NA
TGBp3 +++ NA
CP +++ NA
TGBp1 TGBp1 +++ +++ +++
TGBp1 TGBp2 +++ NA
TGBp1 TGBp3 +++ NA
TGBp3 TGBp1 +++ NA
TGBp3 TGBp3 +++ NA
CP CP +++ +++ +++
a

“⁎”, plasmid expression AD domain (pGADT7) and BD domain (pGBKT7) are added.

b

“+”, yeast colonies that grew on SD medium (Lacking Trp and Leu). “−”, yeast colonies that did not grow on SD medium (lacking Trp and Leu).

c

“+”, yeast colonies that grew on SD medium (Lacking Trp, Leu, His and Ade). “−”, yeast colonies that did not grow on SD medium (Lacking Trp, Leu, His and Ade).

d

“+”, yeast colonies that were blue. “NA” indicates yeast colonies did not grow and no blue histochemical stain was observed.

e

Plasmids containing T-antigen-AD and murine p53-BD were provided by the manufactory and used as positive controls.