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Inferior Frontal Gyrus Traditionally, IFG or the Broca’s area (see Figure 1 ) has been thought to be specialized for syntactic processing and speech [see Price, 2000, for a review]. In neuroimaging studies, the anterior portion of the left IFG (BA 47 and FO) has been implicated in semantic processing [see Poldrack et al., 1999, for a review] and the posterior left IFG (BA 44/45) for syntactical processing [Bookheimer, 2002; Dapretto & Bookheimer, 1999] as well as phonological processing, such as phoneme mon itoring or rhyme judgments [Poldrack et al., 1999; Roskies et al., 2001; Temple et al., 2003]. In addition, the bilateral IFG (BA 45/47) activity was found when children processed semantics [Brauer & Friederici, 2007; Chou et al., 2006] and syntax [Brauer & Friederici, 2007] in sentential level. In terms of the involvement of the IFG area in the ToM development, several neuroimaging studies in children found activity in the IFG while the child participants engaged in facial imitation [Dapretto et al., 2006], story- and cartoon-based irony [Wang et al., 2006a; 2006b] and ToM [Kobayashi et al., 2007a; Moriguchi et al., 2007] tasks. We found a three-way interaction in the left IFG (BA 45) for children and adults [Kobayashi, Glover, & Temple, 2007a]. Children employed this area more for the cartoon ToM condition, yet the adults used this area more for the story ToM co ndition. Similarly, in Wang et al.’s (2006a) study on irony processing, children recruited the left IFG (BA 44 and 45) more than adults. Moriguchi et al. (2007) also found act ivity in the right IFG (BA 45) when children/adolescents processed animation-based ToM task. These results may suggest that the IFG is important for ToM processing especially during childhood because of its role as a language center. However, the fact that some of the developmental ToM brain imaging studies found the IFG activity during the nonverbal tasks [Kobayashi, Glover, & Temple, 2007a; Moriguchi et al., 2007] may indicate that IFG is important for ToM development because of its involvement in inhibitory control. Increasing evidence suggests that bilateral IFG is selectively involved in working memory-related response inhibition [Bunge et al., 2002; Garavan et al., 1999; see also Aron, Robbins, & Poldrack, 2004, for a review]. The greater activity in this area may represent a greater effort to inhibit the immediate and more salient (but wrong) responses in the ToM/irony st ories/cartoons in children than in adults. Another alternative interpretation is that the IFG plays an important role in processing ToM during childhood because of the human mirror neurons that are localized in this area [Agnew, Bhakoo, & Puri, 2007; Oberman & Ramachandran, 2007; Saxe, 2005]. In line with Chiyoko Kobayashi 16this conjuncture, several adult brain imaging studies implicated this area in nonverbal imitation [Buccino et al., 2004; Grèzes, Frith, & Passingham, 2004; Heiser et al., 2003] and ToM [Brunet et al., 2000; German et al., 2004; Kobayashi et al., 2007a] . The IFG activity in children during the nonverbal ToM [Kobayashi et al., 2007a; Moriguchi et al., 2007] and related social cognitive tasks [Dapretto et al., 2006; Wang et al., 2006b] may support this hypothesis given that nonverbal tasks do not usually involve language processing. However, since adults especially seem to process nonve rbal ToM tasks verbally [Kobayashi et al., 2007a; Newton & de Villiers, 2007] and since the mirror neuron system is closely associated with language system in humans [Gallese, 2007; Oberman & Ramachandran, 2007; Siegal & Varley, 2002], future studies need to examine precisely to how much extent the human mirror neuron system is involved in ToM and language development.
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