An anti-saccade, which is a saccade directed toward a mirror-symmetrical po
sition in the opposite visual field relative to the visual stimulus, involv
es at least three separate operations: covert orienting, response suppressi
on, and coordinate transformation. The distinction between pro-and anti-sac
cades can also be applied to pointing. We used fMRI to compare patterns of
brain activation during pro- and anti-movements, to determine whether or no
t additional areas become active during the production of anti-movements. I
n parietal cortex, an inferior network was active during both saccades and
pointing that included three foci along the intraparietal sulcus: 1) a post
erior superior parietal area (pSPR), more active during the anti-tasks; 2)
a middle inferior parietal area (mIPR), active only during the anti-tasks;
and 3) an anterior inferior parietal area (aIPR), equally active for pro- a
nd anti-movement. A superior parietal network was active during pointing bu
t not saccades and included the following: 1) a medial region, active durin
g anti-but not pro- pointing (mSPR); 2) an anterior and medial region, more
active during pro- pointing (aSPR); and 3) an anterior and lateral region,
equally active for pro- and anti-pointing (lSPR). In frontal cortex, areas
selectively active during anti-movement were adjacent and anterior to area
s that were active during both the anti-and pro- tasks, i.e., were anterior
to the frontal eye field and the supplementary motor area. All saccade are
as were also active during pointing. In contrast, foci in the dorsal premot
or area, the anterior superior frontal region, and anterior cingulate were
active during pointing but not saccades. In summary, pointing with central
gaze activates a frontoparietal network that includes the saccade network.
The operations required for the production of anti-movements recruited addi
tional frontoparietal areas.