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. 2011 Aug 12;20(22):4311–4323. doi: 10.1093/hmg/ddr357

Table 1.

Quantitative analysis of 15q11.2–13.3 chromatin condensation

Subregion 15q11.2 15q12–13.1 15q13.2–13.3 Total 15q11.2–13.3 Control 6p22.3
PWS-IC-binding sites in neurons 25 16 27 68 5
PWS-IC-binding sites in neuroblasts 85 42 66 193 19
Total base pairs (TBP) 4 900 000 4 800 000 3 400 000 13 100 000 2 915 400
Neuronal PWS-IC-binding frequency (sites/106 TBP, row 2/row 4) 5.10 3.33 7.94 5.19 1.71
P= probability that the number of PWS-IC interactions is at least as low by chance 0.77288 0.09760 0.99873 0.94464 0.00629
P= probability that the number of PWS-IC interactions is at least as high by chance 0.30126 0.93962 0.00266 0.07900 0.99800
Neuroblast PWS-IC-binding frequency (sites/106 TBP, row 3/row 4) 17.35 8.75 19.41 14.73 6.52
P= probability that the number of PWS-IC interactions is at least as low by chance 0.99997 0.02555 0.99999 0.99999 0.00298
P= probability that the number of PWS-IC interactions is at least as high by chance 0.00004 0.98258 0.00001 0.0000007 0.99848
Decondensation ratio (row 8/row 5) 3.40 2.63 2.44 2.84 3.81
MeCP2-binding sites in neurons 9 15 38 62 10
MeCP2-binding frequency (sites/106 TBP, row 12/row 4) 1.84 3.12 11.18 4.73 3.43
MeCP2 sites/106 TBP in 15q13.2–13.3 divided by the total number of MeCP2 sites 6.07 3.58 1.0 2.36 3.26

The table summarizes chromatin condensation and MeCP2-binding density in subregions of 15q11.2–13.3 chosen based on PWS-IC interaction density in neuroblasts and a control 6p22.3 locus. 15q11.2–13.3 subregions 15q11.2, 15q12–15q13.3 plus 15q13.2–15q13.3 as shown in Figure 1 were assayed for PWS-IC interactions in neurons and neuroblasts (rows 2 and 3). Next the total number of PWS-IC sites was divided by the total number of base pairs in 15q11.2–13.3 subregions (row 4) to give the frequency of interaction for each region in rows 5 and 8. Next, a probability of obtaining the number of PWS-IC interactions at least as low or as high as observed was calculated in rows 6, 7, 9 and 10. To determine levels of chromatin decondensation with neuronal differentiation for each region, the frequency of PWS-IC sites per base in neuroblasts was divided by the frequency of PWS-IC sites in neurons as shown in row 11. Total MeCP2-binding sites (row 12) were divided by total base pairs (row 4) to calculate MeCP2 sites per TBP (row 13). MeCP2 sites/TBP for 15q13.2–15q13.3 were divided by MeCP2 sites/TBP for the other subregions as a means of comparison (row 14).