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Fig. 6. Mislocalization of Sall4 from the heterochromatin by a truncated Sall1
that functions in a dominant-negative manner. (A) Requirement of
the C-terminal zinc finger (Zn4) of Sall4 for heterochromatin localization
(rectangle). Zn4 is also sufficient for heterochromatin localization (broken
outline). Mutants of Sall4-GFP fusion were expressed in NIH 3T3 cells.
Zinc-finger clusters are categorized as Zn1, Zn2, Zn3 and Zn4, as shown.
(B) Requirement of the C-terminal zinc fingers (Zn4 and Zn5) of Sall1
for heterochromatin localization (rectangle). Zn4 and Zn5 are also sufficient
for heterochromatin localization (broken outline). Mutations in Zn2 and Zn5
also show a defect in heterochromatin localization, though these two clusters
are not sufficient for proper localization in the heterochromatin. (C)
Co-transfection of truncated Sall1
(Sall11-435-DsRed) and Sall4-GFP into NIH 3T3
cells. Heterochromatin localization of Sall4 is disrupted by C-terminally
truncated Sall1.