Fig. 3 | Nature Communications

Fig. 3

From: Nuclear lamina integrity is required for proper spatial organization of chromatin in Drosophila

Fig. 3

TADs respond differentially to NL disruption. a Hi-C map showing a total chromatin interaction profile (left half of the map), or subtraction map (Lam-KD - control) (right half of the map) at a 2.8-Mb region of chromosome 2 L. Chromatin annotation in S2 cells40 and LADs annotation in Kc167 cells28 are shown below. b, c Dependence of intra-TAD ACF changes upon Lam-KD on the LAD coverage (b), or on the proportion of “red” and “purple” chromatin types40 (c) within these TADs. Trend line is in red. d Separation of TADs into four groups according to the Jaccard similarity coefficient. Box plots show the proportion of active chromatin (“red” (active TSS) plus “purple” (elongation) chromatin types40) and LAD coverage28 within each group. e Transcription level in the four groups of TADs according to RNA-seq in control S2 cells. f Changes of intra-TAD ACF between Lam-KD and control cells in the four groups of TADs. g Variances of log2(FC) of the intra-TAD ACF upon Lam-KD compared to control cells in the four groups of TADs. ***P < 0.001, *P < 0.05 in a Levene’s test. h Changes of total transcription (left panel) and H3 pan-acetylation (right panel) levels between Lam-KD and control cells in the four groups of TADs. i Changes of ACF values, H3 pan-acetylation and total transcription in the inter-TAD regions between Lam-KD and control cells. See Fig. 1g legend for description of boxplot elements represented on panels (df), (h) and (i). In panels e, f, h, i, ****P < 0.0001, ***P < 0.001, **P < 0.01, *P < 0.05, NS non-significant difference (P> 0.05) in a Wilcoxon test

Back to article page