Evaluation of putative KRIT1 localization sequences.
A, schematic of KRIT1 noting the sequence of
NLS1, NES, and NLS2 as well as domain boundaries.
B, CHO cells overexpressing GFP-tagged
KRIT1 constructs were plated on fibronectin, fixed 24 h later,
and stained with DAPI to identify nuclei. Representative images
are shown; bar, 10 μm.
C, relative amount of GFP intensity in the
nucleus compared with the integrated GFP intensity of the entire
cell. Boxes, 25th through 50th and 50th through
75th percentile; whiskers, 5th through 95th
percentile (n = 85–157 cells from 4
independent experiments). *, p ≤ 0.0001
as determined by a one-way ANOVA with Tukey's correction for
multiple tests.