Cortical areas for planning sequences before and during movement

Abstract

Production of rapid movement sequences relies on preparation before (pre-planning) and during (online planning) movement. Here, we asked how different cortical sensorimotor areas contribute to these processes. Human participants performed three single-finger and three multi-finger sequences in a delayed movement paradigm. During preparation, 7T functional MRI revealed that primary motor (M1) and somatosensory (S1) areas showed pre-activation of the first movement, even though the overall activation level did not change from baseline. During production, the activity in M1 and S1 could be explained by temporal summation of activity patterns corresponding to constituent fingers. In contrast, dorsal premotor (PMd) and anterior superior parietal lobule (aSPL) showed substantial activation during preparation of multi-finger as compared to single-finger sequences. The same regions were also more activated during production of multi-finger sequences, suggesting that the same areas are involved in both pre- and online planning. Nonetheless, we observed small but robust differences between the two contrasts, suggesting preferential involvements of these areas in pre- and online planning. Multivariate analysis revealed sequence-specific representations in both PMd and aSPL, which remained stable across both preparation and production phases. This suggests that these areas maintain a sequence-specific representation before and during sequence production, likely guiding the execution-related areas. Significance StatementUnderstanding how the brain orchestrates complex behavior remains a core challenge in human neuroscience. Here, we combine high-resolution neuroimaging and a carefully crafted design to study the neural control of rapid sequential finger movements, like typing or playing the piano. Advancing prior research, we show that the brain areas involved in planning these movements maintain those representations throughout the execution of the sequence. This representational stability across planning and execution suggests an intricate connection between these processes. Our results shed light on the nuanced contributions of different cortical areas to different aspects of coordinating skilled movement. This work is well placed to inform future research in animal models and the development of targeted interventions against movement disorders.