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. 2022 Jul 7;121(15):2895–2905. doi: 10.1016/j.bpj.2022.07.001

Figure 1.

Figure 1

Transitions in the kinetic model. (A) The forward and backward reactions are shown on the left and right, respectively. The left depicts the enzyme-induced modification, UM, at the ith nucleosome. The right sketches the removal of the mark, MU, from the jth nucleosome. Modifications to unmarked (U) nucleosomes and removal of marks from the M-type nucleosomes are shown by arrows. Important mediators relevant to the spreading processes are shown in color: the nucleation site (NS) is in green, and U (M) nucleosomes are shown in yellow (red). Some or all elementary transitions are considered simultaneously, representing four separate spreading mechanisms (see Fig. S1). The forward reaction occurs if an unmarked nucleosome i has a neighbor nucleosome in the modified state with a probability P1D+(i) (orange arrow) or with a probability P3D+(i) if it is in the spatial vicinity of an NS/modified nucleosome (purple arrow). The backward reaction can always proceed with a probability PN(j), indicated by a black dashed arrow. The MU reaction may also depend on the presence of other unmarked nucleosomes. In such cases, neighbor nucleosomes might induce the MU transition in nucleosome j with a probability P1D(j) (cyan arrow), while U nucleosomes in the spatial vicinity of j may induce the reverse reaction with probability, P3D(j) (magenta arrow). (B) Asymmetric spreading from the NS (green) and non-NS sites (red). The forward rate for the non-NS sites is scaled by a factor of α compared with that for the NS site. Typically, we use α1 in this study, which means that the ability of spreading of a non-NS site is much smaller than that of the NS site. To see this figure in color, go online.