Int J Med Sci 2013; 10(9):1136-1148. doi:10.7150/ijms.6121 This issue Cite
1. German Cancer Research Center, Dept. of Biophysics of Macromolecules, INF 580, D-69120 Heidelberg, Germany;
2. German Cancer Research Center, Dept. of Medical Physics in Radiology, INF 280, D-69120 Heidelberg, Germany;
3. German Cancer Research Center, Genomics Proteomics Core Facility HUSAR Bioinformatics Lab, INF 580, D-69120 Heidelberg, Germany;
4. German Cancer Research Center, Genomics and Proteomics Core Facility High Throughput Sequencing, INF 580, D-69120 Heidelberg, Germany.
The highly organized DNA architecture inside of the nuclei of cells is accepted in the scientific world. In the human genome about 3 billion nucleotides are organized as chromatin in the cell nucleus. In general, they are involved in gene regulation and transcription by histone modification. Small chromosomes are localized in a central nuclear position whereas the large chromosomes are peripherally positioned. In our experiments we inserted fusion proteins consisting of a component of the nuclear lamina (lamin B1) and also histone H2A, both combined with the light inducible fluorescence protein KillerRed (KRED). After activation, KRED generates reactive oxygen species (ROS) producing toxic effects and may cause cell death. We analyzed the spatial damage distribution in the chromatin after illumination of the cells with visible light. The extent of DNA damage was strongly dependent on its localization inside of nuclei.
The ROS activity allowed to gain information about the location of genes and their functions via sequencing and data base analysis of the double strand breaks of the isolated DNA. A connection between the damaged gene sequences and some diseases was found.
Keywords: Chromatin architecture, DNA-topology, fluorescent proteins, genome architecture, KillerRed, Photo-Dynamic-Therapy, subcellular localization.
The decryption of the human genome sequences in 2001 was the jump start for the rapidly expanding genome research [1, 2]. Despite of the gained genomic data of bioinformatics, it is difficult to understand the operating mode of the complex genome. Speculations suggested a critical role of a DNA's spatial patterns in the coordination of transcription [3-6]. Investigations regarding the development of models of chromosome arrangements go back to the turn of the 20th century, first documented in 1885 by Rabl and in 1909 by Boveri [7, 8]. The pioneering work of the Cremer groups in 1996 and 2006 contributed to the acquirement of data reflecting the topologic organization of the genome and of the core principle of the nuclear architecture with functional genome organization [9-11]. Meanwhile the highly organized DNA architecture inside of nuclei is considered as accepted in the scientific world [12-15]. Localization studies of human chromosomes indicate a central nuclear position of small chromosomes whereas the large chromosomes are peripherally positioned . The well investigated basic structural 10 nm fiber is composed of nucleosomes consisting of histone octamers built up of histones H2A, H2B, H3, and H4 acting as structural proteins with DNA wrapped around and histone H1 in the internucleosomal region [17-20]. Furthermore, the limited capacity of the volume of the nuclei requires a compact DNA packing with well-regulated chromatin structures like fibers of different size.
Several groups documented gene regulation processes controlled by histone acetylation and deacetylation which are supposed to be independent of the gene localization inside of the nuclei [21-23]. The correlation of the nuclear organization of chromosomes to their banding patterns was well documented [24, 25] and comprehensively reviewed and discussed by Santoni . The spatial arrangement of genes, centromeres and chromosomes inside nuclei and their changes are documented [27, 28]. The inner surface of the nuclear envelope is lined with the nuclear lamina (thickness ~30-100 nm) consisting of components like the lamin B1 protein [29, 30]. Its function is critical in gene regulation [31-34] and a change can result in different clinical pictures like the Emery-Dreifuss muscular dystrophy pathophysiology , the Hutchinson-Gilford progeria syndrome  and further laminopathic diseases . However, to which extent these illness patterns could be fostered and caused in cells by cell-externally and -internally induced degenerative processes remains to be investigated.
The impact of reactive oxygen species (ROS) on biological systems was intensively investigated. The meaningful role of free radicals in processes leading to cellular stress causing genetic pathogenesis, like aging, Alzheimer's disease, arteriosclerosis and cancer, as well as inflammatory processes, are without contradiction. Genetoxic effects by external stimuli could also be generated by photolysis effects of light inducible fluorescence proteins (FPs)  like KillerRed (KRED). They produce oxygen-generated ROS, like the radicals O2•-, the highly reactive hydroxyl-radical OH•, the peroxide radical ROO•, as well as the active oxygen species (singlet-oxygen 1O2). Disregarding parameters like the concentration gradient and the continuity equation, the self-diffusion of water with the coefficients 3.94×10-9 m2 × s-1 at 50°C; 2.29×10-9 m²·× s-1 at 25°C and 1.26×10-9 m²·× s-1 at 4°C  underlies the Brownian motion as a fluctuation phenomenon according to the mean squared displacement (MSD) [40-43]. This indicates a very short-range of the ROS's average path length and thus a very small spatially limited sphere of action (~0.1 µm ø).
The ultra-short-lived (~1 µs) singlet oxygen and the superoxide [44, 45] were investigated by the Bulina group . These toxic effects may cause cell death as observed in our illumination studies of DU 145 human prostate cancer cells  after transfection with the recombinant KRED-lamin B1 plasmid . The KRED plasmid and the corresponding protein were first described by the Bulina and Lukyanov groups [46, 49]. The protein showed cell toxicity after transfection/transformation and cells' exposition to visible light. The extent of damage was cell type independent [48, 50], but strongly dependent on the localization inside of cells  and more precisely, in specific intranuclear positions, as site of action of the activated KRED protein.
Based on Cremer's postulation, mentioned above, and the high cell damaging potential of KRED by visible light, the ROS induced double strand breaks in the DNA should happen close to the lamin-“marbleized” inner surface of the nuclear envelope. The question of the affected genes remains to be answered. Therefore we isolated DNA from DU 145 cell nuclei after transfection or transformation and cloning the cells with the KRED-lamin B1 plasmid. The nuclei were isolated and illuminated with white light with a wave length above 400 nm. As a control organism we used nuclei of the same cell line transfected with the identical plasmid but coding for histone H2A-KRED. The DNA fragments were isolated, sequenced and the affected genes were identified. We used the Illumina Library preparation and sequencing methodology, and characterized sequences with the HUSAR software tools . We identified 24,502 genes (offering read counts between 6,824-1) in the KRED-lamin B1 probe harvested 30 min after light illumination and 24,300 genes (offering read counts between 6,039-1) in the KRED-lamin B1 probe 60 min after light illumination of the KRED-lamin B1 transfected DU 145 cells. In the probe with the histone H2A-KRED transfected cells 25,870 affected genes (offering read counts between 15,664-1) were detected 30 min after illumination.
The KRED-lamin B1 probes were investigated at two time points to control the whole procedure. The values were compared to histone H2A-KRED with a wide nuclear distribution.
For the investigation of the KRED-induced DNA damage we used the following vectors (Figure 1) coding for the fusion proteins KRED-lamin B1 and histone H2A-KRED .
(a) Physical map of the vector expressing the fusion protein KRED-lamin B1. The lamin B1 was inserted into the MCS. (The lamin B1 sequence was kindly provided by H. Herrmann, this institute). (b) Physical map of the vector expressing the histone fusion protein H2A-KRED. The histone H2A was inserted into the MCS.
The stable cell line was established after transfection of the KRED-lamin B1 expressing vector (Supplementary Material: Figure 1a) followed by cloning of positive cells for some weeks. The KRED-lamin B1 transfected cells were gained under selective pressure with G-418. To create a histone-KRED expressing cell line the histone-H2A-KRED vector (Supplementary Material: Figure 1b) had to be transiently expressed; no cell line could be established because of cell death. Both, DU 145 human prostate cancer cells expressing the fusion proteins were cultured and maintained in RPMI 1640 medium (Gibco, USA) supplemented with FCS 10% (Biochrom, Germany) and L-glutamin 200 mM (Biochrom, Germany) at 37°C in a humid 5% CO2 atmosphere. For the experiments the cells were seeded into Petri dishes (5 × 150 cm2), and were washed with HBSS (Hank's balanced salt concentration, PAN, Germany). After trypsinization of the cells (3 × 106) they were harvested in RPMI 1640 (Gibco 11835) with 2% FCS and centrifuged (800 rounds/min, 5 minutes; Heraeus, Germany). After resuspension of the cells in HBSS the cell number was adjusted to 1 × 106 cells × ml-1 with the DNA repair inhibitor ABT-888  (5 µM) HBSS. The extraction of nuclei followed.
DU 145 human prostate cancer cells (1.2 × 106 cells in 3 Petri dishes/10 cm diameter) were transfected with the both plasmids according to Invitrogen's user manual. Clones were generated over weeks by selection pressure in cell culture with G-418 (Geneticin®) 500 µg/ml final concentration. With the fusion plasmid (H2A-KRED) transfected cells no cell line could be established, the cells were harvested around 48 - 72 h after transfection.
This procedure was accomplished completely on ice. All reaction solutions contained the PARP inhibitor ABT-888 (5 µM). After cell trypsinization the cell pellet was washed with HBSS (PAN P04-49505) first, then with isotonic Tris (137 mM NaCl; 5mM KCl; 0.3 mM Na2HPO4×2H2O). After a final wash step with isotonic HEPES buffer [2-(4-(2-hydroxyethyl)-1-piperazinyl)-ethane sulfonic acid] 50 mM / pH8; 220 mM sucrose; 0.5 mM CaCl2; 5mM MgCl2 the nuclei were pelleted (1,000 rounds/ min, 5 minutes in a centrifuge, Heraeus Germany). The nuclei were resuspended in 10 ml isotonic HEPES supplemented with 10% NP40, final concentration 0.25%, then vortexed in steps 60s first, followed by three steps à 30s with intervals for 30s on ice. The solution was adjusted to 50 ml with isotonic HEPES. After the next centrifugation (2,000 rounds/ min, 5 minutes; Heraeus, Germany) and resuspension of the pellet in 25 ml solution of isotonic HEPES endued with 200 mM sucrose and 5 µM ABT-888, the nuclei were prepared for illumination studies.
The probes with the aforementioned suspensions of the DU 145 cells' nuclei (1 × 106) × ml-1 were placed in Petri dishes with glass bottom (ibidi uncoated) under a full-spectrum sunlight bulb with 32 Watt (www.androv-medical.de) in a distance of 1 cm.
The illumination took place at 20°C; the probes were placed on an aluminium block, cooled by a fan to keep the room temperature. The 32 Watt bulb has a measured intensity of 20,000 lux in a 1cm distance, which reflects a normal daylight in a cloudy summer . As determined in earlier experiments, we used the two illumination times: 30 minutes for the measurements of the H2A-KRED probes and for the KRED-lamin B1 probes also 60 min.
To avoid RNA contamination of our DNA fragments an enzymatic treatment of the nuclei with RNase was conducted immediately after illumination. The probes were centrifugated (10,000 rounds/min; 10 minutes). The nuclei were resuspended in 300 µl solution of 20 mM Tris (pH8) with 50 µg × ml-1 RNase for 5h and incubated at 37°C and at room temperature overnight. An additional treatment with a 50 µg × ml-1 Proteinase K /0.1% SDS mixture, at 37°C for 5 h and overnight followed to isolate the DNA.
The isolated DNA was precipitated with ethanol (70%) and washed twice. Then the DNA fragments were purified in a preparative electrophoresis through an agarose gel in a TAE 1% (Tris-acetate-EDTA) buffer (Figure 2). Small molecules with the most DSB-hits were selected (200 -1,000 bp) with selection of the corresponding DNA sizes by marker bands. The agarose piece was cut out without ethidium bromide and UV light and subsequently frozen at -20°C for at least 1 h followed by centrifugation (3,000 rounds × min-1) at 15°C in 50 ml purification cartridges (Falcon) to isolate the DNA. The complete removal of solvent was terminated after 90 min centrifugation. The probes were concentrated in Centricon-10 cartridges (Millipore, USA) by centrifugation at 15°C and 5,500 rounds × min-1 for 10 min, and then washed in 10 mM Tris pH7, 0.1 mM EDTA before sequence analysis.
The fragmented DNA was size selected in a range of 200 - 500 bp using E-Gel® Electrophoresis System and appropriate 1% E-Gel® Ex precast agarose gel (Invitrogen, Cat No. G4010-01) (Figure 2). DNA fragments were purified from agarose gels according to the QIAquick® Gel Extraction Kit protocol (Qiagen, Cat No. 28704) and the DNA quantified using Qubit® flourometer (Invitrogen, Qubit® dsDNA HS Assay Kit, Cat No. Q32854). We started with 450 ng of each probe. Illumina Libraries were prepared using 10 ng of size selected DNA and the NEBNEXT® ChIP-Seq Library Prep Master Mix Set for Illumina (Cat No. E6240L) following the instructions of the manufacturer with the following modifications. We performed a PCR with 3 µL of adapter ligated DNA and 10 amplification cycles. Illumina Libraries were validated using Agilent 2100 Bioanalyzer® (High sensitivity DNA Kit, Cat No. 5067-4626) and Qubit® flourometer (Invitrogen, Qubit® dsDNA HS Assay Kit).
The final libraries were clustered on the cBot (Illumina) according to the instructions of the manufacturer with a final concentration of 9 pM spiked with 1% ΦX control v3 (Cat No. FC-110-3001) using TruSeq SR Cluster Kit v3 (Cat No. GD-401-3001). Sequencing on HiSeq2000 (51 bp single read mode) was performed using standard Illumina protocols and the 50 cycles TruSeq SBS Kit v3 (Cat No. FC-401-3002).
depicts the preparative DNA gel with the lanes containing the DNA fragments for sequencing (white framed). The right lane represents the marker DNA sequence bands; (bp = base pair; M = DNA-marker).
The significant annotation clusters of the 100/600 affected genes were packaged (100-genes bundles). The normalized data (Benjamini & best p-values; cut off at 1.0E-3) are represented in Table 2. The graphical determination and illustration of the KRED-lamin B1 and the H2A-KRED damaged genes as genetic groups following GO annotations are shown in Table 7. We used the Blast2GO tool (http://www.blast2go.com/b2glaunch) for functional annotation of FASTA nucleotide sequences (http://husar.dkfz-heidelberg.de/menu/w2h/w2hdkfz/). BLAST identifies homologous sequences. MAPPING retrieves GO terms. ANNOTATION performs reliable GO functions and enrichment scores. ANALYSIS produces the graphical display of annotation data with GO graphs (http://www.ncbi.nlm.nih.gov/omim).
The determined gene clusters were defined for annotation, visualization and integrated discovery using the Database for Annotation, Visualization and Integrated Discovery (DAVID) (http://david.abcc.ncifcrf.gov/home.jsp).
The comparison of the affected lamina-located genes versus the genes widely spread over the total chromatin requires a normalization of the measured read counts. Due to the short-lived ROS, especially affected are genes which are located in immediate vicinity to the areas of ROS-formation in the close vicinity of the inner nuclear shell (lamin B1) or the surface of the inner chromatin. We compared the DNA fragmentation by induction of ROS with visible light. This light induces the KillerRed fusion proteins KRED-lamin B1 and histone H2A-KRED to create ROS. The gained sequence data were directly correlated to the ROS-affected genes of the whole inner nuclear chromatin.
The intention was to find the ds-DNA fragments broken by the induced KRED generated ROS in different loci of the nuclei. The data should give information about the spatial distribution of these DNA pieces. The ROS-affected genes are displayed in the plots in descending order according the amount [read counts] of DNA damages. We tested 30 (Figure 3) and 60 min (shown in Figure 3a, Supplementary Material) after exposition of nuclei to visible light the KRED-lamin B1 induced ds-DNA breaks.
After normalization of the read counts of the lamin B1 (30 min) and the histone H2A (30 min) probes, they were compared by divison (read counts-lamin through read counts-histone). A schematical description is given in C: lamin-localized genes (Table 4) and D: whole chromatin -localized genes (Table 5).
We identified 24,502 affected genes (offering read counts between 6,824-1) in the 30 min probe and 24,300 genes (offering read counts between 6,039-1) in the 60 min probe (Figure 3a, Supplementary Material). To analyze these hits, we focused on the RefSeq IDs with the highest number of read counts of DNA damages in the four most affected genes after 30 min: the NR_003594, which corresponds to REXO1L2P, featured 6,824 counts, closely followed by the NM_003482 (6,806 counts) and NM_005560 (5,420 counts). The independently prepared 60 min probe showed the same order of highest affected genes but with a little lower read counts (6,039), and the IDs NM_003482 (4,973 counts) and NM_005560 (5,420 counts) (as shown exemplarily in Supplementary Material: Table 1a); (further affected genes are listed in detail in Supplementary Material: Table 1a).
the plot represents the curves of the read counts (ordinate) 30 min after light exposition; the abscissa lists the affected genes in descending read counts order down to 100. (n = read count). The ordinate shows the number of counts.
lists the ROS affected genes offering the highest damage read count numbers. It is a description of the four genes of the KRED-lamin B1 probe with the highest read counts (details shown in Supplementary Material: Table 1a, right column).
|RefseqID||Read Counts||Gene Symbol||Description||Physical map|
|30 min||60 min|
|NR_003594||6,824||6,039||REXO1L2P||RNA exonuclease 1 homologue-like 2||19p13.3 [R]|
|NM_003482||6,806||4,973||MLL2||histone-lysine N-methyltransferase MLL2||12q13.12 [G]|
|NM_005560||5,420||3,793||LAMA5||laminin subunit alpha-5 precursor||20q13.33 [R]|
|NM_001164462||4,688||4,544||MUC12||mucin-12 precursor||7q22.1 [R]|
lists the annotation clusters 1-3 with the enrichment scores 6.74; 3.1; and 2.92 of the gene bundle of the most prominent 7 of 100 entries which offer the highest read counts of the KRED-lamin B1 probe 30 min after illumination in DAVID functional annotations analysis which gave clusters of GO term enrichment.
lists the 30 min probe of the ROS affected genes offering the highest read count number in the histone H2A with fragmented DNA.
|Refseq ID||Read Counts||Gene Symbol||Description||Physical map|
|NM_003511||15,664||HIST1H2AL||histone H2A type1||6p22.1 [G]|
|NM_001190470||3,185||MTRNR2L2||humanin-like protein 2||5q14.1 [G]|
|NR_003594||2,491||REXO1L2P||RNA exonuclease 1 hom.-like 2 (pseudo)||19.13.3 [R]|
|NR_002728||2,450||KCNQ1OT1||antisense transcript 1 (non-protein coding)||11p15.5 [R]|
lists the first 13 of the 57 most affected genes which show read counts solely in the lamin B1 probe but not in the H2A-KRED control (schematized shown in Table 6, which demonstrates their possible spatial intranuclear localization). The right column describes the physical mapping of the chromosomal regions.
|Refseq ID||Read Counts||Gene Symbol||Description||Physical map|
|NM_001127482||12550||SPRYD7||SPRY domain containing 7||13q14.2 [R]|
|NM_001003796||6584||NHP2L1||non-histone chromosome protein 2-like 1||22q13.2 [G]|
|NM_001039210||6428||ALG13||asparagine-linked glycosylation 13 homolog||Xq23 [G]|
|NM_001004333||6331||RNASEK||RNase kappa||17p13.1 [R]|
|NM_001035223||5688||RGL3||Ral guanine nucleotide dissoc stimul-like 3||19p13.2 [G]|
|NM_001114106||5055||SLC44A3||solute carrier family 44, member 3||1p21.3 [G]|
|NM_001099410||4953||GPRASP1||G-protein coupled receptor-assoc sort protein 1||Xq22.1 [R]|
|NM_001105538||4826||MYBBP1A||myb-binding protein 1A||17p13.2 [G]|
|NM_001124759||4339||FRG2C||FSHD region gene 2 family, member C||3p12.3 [G]|
|NM_001099455||4305||CPPED1||calcineurin-like phosphoesterase dom protein 1||16p13.12 [G]|
|NM_001171799||3906||TRIQK||Triple QxxK/R motif-containing protein||8q22.1 [R]|
|NM_001134364||3613||MAP4||microtubule-associated protein 4||3p21.31 [R]|
|NM_001139518||3409||PRKRA||protein kinase interferon-inducible ds RNA dependent||2q31.2 [G]|
lists the first 4 of the 25 most affected genes which show read counts in the H2A-KRED control but not in the lamin B1 probe.
|Refseq ID||Read Counts||Gene Symbol||Description||Physical map|
|NM_001146197||3804||CCDC168||coiled-coil domain containing 168||13q33.1 [G]|
|NM_001127464||3247||ZNF469||zinc finger protein 469||16q24.2 [G]|
|NM_001042603||2974||KDM5A||lysine (K)-specific demethylase 5A||12p13.33 [R]|
|NM_001110781||2580||SLC35E2B||solute carrier family 35, member E2B||1p36.33 [R]|
The graph (Figure 3) gives insight into the extent of genetic breakpoints caused by ROS versus the affected genes. The different annotation clusters generated by DAVID software are listed in the following tables and contain the affected genes arbitrarily bundled in amounts of 100. Table 2 lists the prominent 7 genes of the first 100 entries in this functional annotations analysis which gave clusters of GO term enrichment. Further 600 genes, combined to bundles of 100 genes, are listed in the Supplementary Material (Table 3a - 7a).
We also determined the spatial localization of genes close to the nuclear lamina (radius 0.1 µm): The first hint is given by the ROS damaged genes following descending read counts. (The corresponding ONIM IDs are listed in Table 1a, right column (Supplementary Material).
As a control we identified the ROS-affected genes distributed across the nuclear chromatin using the recombinant fusion protein histone H2A-KRED whose histone part is an essential element of the whole chromatin structure. The ROS affected genes are displayed in plots according to the extent [read counts] in a descending order of DNA damages (Figure 4).
Our second probe, the histone H2A-KRED should be distributed over the whole nuclear chromatin in a 3-dimensional way.
We identified 25,870 affected genes (offering read counts between 15,664-1) in the 30 min probe (Figure 4). It is particularly noticeable that the RefSeq Id NM_003511 exhibits by far the highest lot of read counts of DNA damages in the affected genes after 30 min. Behind this histone H2A type 1 (HIST1H2AL) gene followed the MTRNR2L2 encoding the humanin-like protein 2 in a clear numeric distance with 3,185 read counts, and with 2,491 read counts the RefSeq ID NR_003594 which corresponds to REXO1L2P. This is closely followed by the RefSeq IDs NR_002728 corresponding to the KCNQ1OT1 gene (2,450 read counts) and the NM_001190702 (2,414 read counts) encoding the humanin-like protein 8. Here it should be mentioned that REXO1L2P was aleady identified in the lamin B1 probe.
The RefSeq ID NM_003482 (2,266 read counts) corresponds to the histone-lysine N-methyltransferase gene encoding the MLL2 protein.
After normalization of the data we compared the affected genes of the lamin B1 probe with the histone H2A probe. The search clearly shows read counts in the lamin B1-KRED probes not present in the histone H2A-KRED control. 1,065 ROS-affected genes were detected and after data normalization the genes with the highest amount of read counts are listed in a descending order (12,550-3,409 read counts) in Table 4 and (1,003 read counts) are shown exemplarily in Table 13a, with 57 genes (Supplementary Material).
The spatial localization of these 13 genes which offer the highest read counts in the nuclei is displayed in Table 6 and characterized with the fold change factor range between 371 and 103.
We next compared the normalized data of lamin B1 with the histone H2A probes listed in Table 5 showing the most affected genes of the histone H2A probe.
The comparison of the lamin B1 probe against the H2A probe shows read counts in the spatial H2A-control but not in the lamin B1 probes. 2,432 ROS-affected genes were detected and after data normalization the genes with the highest values (3,804-2,580) are listed in descending order (shown in Table 5) and to 1,003 read counts are shown in Table 14a (Supplementary Material):
These fold change data provide first information concerning the inner nuclear localization with the utmost probability. The factors may provide recommendations for a possible inner nuclear localization and for a reasonably stepwise classification of the ROS-affected genes. The fold change is a quotient formed between the read counts of the lamin B1 probe and the H2A-KRED probe.
Table 6 displays 13 genes featuring a ratio range between the factors 371 and 103 which indicate a clear localization very close to the lamin B1. In contrast, in the middle of the nucleus, 6,348 genes are listed between the fold change factors 0.9 and 0.01 generated by histone H2A-KRED.
The comparison of these fold change factors, as listed in Table 6, shows, that the ranges between 3.7 × 102 and 101 list only 400 genes, whereas the relatively small range of the factors between 101 - 10-1 lists 23,032 genes.
The plot represents the curve of the read counts (ordinate) 30 min after light exposition of the histone H2A-KRED containing nuclei; the axis of abscissa lists the affected genes in descending read counts order. (■ = read count)
illustrates the graphical determination of the damage density and lists the ROS-affected genes according to the read counts' fold change factors in descending order. It represents the radial distribution of the territorial range starting from the inner surface of the nucleus inwardly to the middle of the nucleus. The triangle (lower line) symbolizes the increasing number of damaged genes from the inner surface (lamina) to the center of the nucleus.
DAVID bioinformatics resources allow insight in biological and pharmacological mechanisms and account for a better understanding of the association of DNA damages with genetic diseases [55, 56]. The direct links to the corresponding GO IDs are given from data which are listed in the tables of Supplementary Material.
Additionally, we used the BlastiX program (NCBI Blast2GO, Version 2.6.2), for the appraisal of the FASTA sequences generated by HUSAR software of the listed “100-gene” bundles (see Supplementary Material: Table 3a - Table 7a) with the highest read counts and a Blast Expect Value with the cut off 1.0E-3 of the 600 of most ROS-damaged genes.
Both bundles, the KRED-lamin B1 (Table 2) and the histone H2A-KRED probes (Table 11a Supplementary Material) harbour annotation clusters with the highest enrichment scores and Benjamini values. The Table 7 generates graphics itemized according to the GO annotations of molecular, function, biological process and cellular components.
With these data we generated a graphical determination of the heaviest light damaged functional gene groups of the histone H2A-KRED and KRED-lamin B1 probes (Table 7)
As described in the methods section we used the Blast2GO tool for functional annotation of the FASTA nucleotide sequences. The software BLAST identifies homologous sequences, MAPPING retrieves GO terms, ANNOTATION performs reliable GO functions and enrichment scores and ANALYSIS produces graphical display of annotation data with GO graphs. The comparison data are shown in Table 7.
The NCBI OMIM (Online Mendelian Inheritance in Man) database shows the gene mapping with close connection to human genes and their genetic phenotypes. This helps to understand the relationship between altered genotypes and the resulting clinical entities such as genetic disorders.
Resulting from our Table 1 and Table 1a (Supplementary Material), the four genes with the highest damage read count numbers and the resulting laminopatic diseases are characterized shortly.
shows the contrasting juxtaposition of the mapping the first 100 genes of the KRED-lamin B1 and histone H2A-KRED bundles. These functional groups offer the highest number of read counts 30 min after illumination and DNA damage.
In the lamin B1 as well as in the histone probes we detected highest damage rates of the REXO1L2P. The gene, mapped at the R-band of the chromosome 19p13.3, codes for the RNA 3' exonuclease 1 REX1. HomoloGene data (http://www.ncbi.nlm.nih.gov/homologene/) indicate that this gene is present in the common ancestor of eukaryotes offering orthology from human down to Saccharomyces cerevisia. It is documented as a human pseudogene homologue to the yeast RNase gene D family whose gene products are involved in maturation processes of 5.8S rRNA [57, 58]. Additionally, animal studies demonstrated that the disruption of REX1 influences differentiation and cell cycle regulation of embryonic stem cells .
The MLL2 mapped to the 12q13.12 region (G-band) and is involved in mutations, translocations and duplications between disease genes whose alteration of function is strongly associated with cancer . Diseases of blood forming organs were documented like acute leukemia (ALL)  and in lymphomagenesis like non-Hodgkin lymphoma (NHL) .
The LAMA5 mapped at the R-band of 20q13.33 and its expression is tissue-specific, mainly in brain, placenta, kidneys, lung and skeletal muscles . Laminins are large glycoproteins found in basement membranes where they play a vital role in tissue architecture and cell behaviour. LAMA5 polymorphisms are associated with anthropometric traits, fasting lipid profile, polycystic kidney disease (PKD) and altered plasma glucose levels . Furthermore, the association of the Lama5 protein in organogenesis and placental function during pregnancy is documented [64-66].
The cytogenic location of MUC12 is the R-band of chromosome 7q22.1. It was isolated first by the Williams group in 1999. MUC12 is a member of mucin genes coding for epithelial mucins, large cell surface glycoproteins, involved in cell protection and signalling. Down regulation or loss of function is identified in colorectal cancer (CRC) . The lower expression status is considered as a meaningful independent prognostic factor in states II and III of CRC .
Collecting evidences for the hypothesis of the evolutionary origin of the nucleus and its compartmentalized architecture is a great challenge in the post-genomic era . Chromatin studies demonstrated radial chromosomal arrangements inside of ellipsoid and spherical human cell nuclei . With the knowledge about the spatial arrangement of the intranuclear chromosomal territories it becomes evident, that chromosomes harbouring tight gene clusters are preferably localized in the center. Chromosomes with less genomic clusters are localized more peripherally adjacent to the nuclear lamina and furthermore, the larger chromosomes are positioned even more peripherally . FISH studies of such chromosomes substantiated this chromatin arrangement, demonstrating the preferred nuclear interior localization of gene-rich chromosomes, while the gene-poor chromosomes are accumulated closer to the nuclear lamina [72, 73]. An also well documented feature of the eukaryotic nuclear organization is the observed genome segregation into the transcriptionally active euchromatin and the transcriptionally inactive heterochromatin [74, 75].
Amongst others a further aspect is the cytogenetic classification in R- and G-bands, which might allow more insight into the complex structural chromosomal architecture. The ISCN (International System for Cytogenetic Nomenclature) introduced an ideogram in 1971, which comprehended a diagrammatic representation of banding patterns. With the help of this band morphology of each chromosome and a unique numbering system chromosomal specific bands and regions could be described . These coloured chromosomal regions (banding) were named G-bands, (G for Giemsa) and not coloured R-bands, (R for Revers) [77, 78].
This staining behaviour is not well understood, but this banding allows a clear identification of the human chromosomes. The R-bands mainly consist of GC-bases and are gene rich, especially including housekeeping genes, in contrast, the G-bands have a higher AT content and are mainly occupied by tissue-specific genes . Also CpG islands are specific to R-band exons  and often associated with Alu-sequences, which transcribe non coding RNA with RNA-Polymerase III .
The detected KCNQ1OT1 gene e.g. maps at 11p15.5 (Table 3) and is located inside of a chromosomal R-band and could be considered as an example for a non-protein coding gene whose transcribed RNA is critical in the chromatin conformation [82-84]. This was substantiated with recent data of gene expression comparison studies of differently structured genes and methylation patterns pivotal in gene regulation showing a high conservation between human and bovine .
Genes of the R banding are replicated early in contrast to the genes in G-bands [5, 80, 86, 87].
In case of the replication of chromosomes, the S-phase does not proceed evenly, but at different time points in certain chromosomal areas. Both, the early and the late replication events are properties which are constant and inherited for all chromosomal segments and are considered as a characteristic of a certain cell type. It is important to note O'Keefe's detections: the areas replicating early are preferably arranged in the center of the nucleus. The late replicated chromosomal areas are located predominantly close to the inner surface of the nuclear envelope [88-90].
Adjacent to the lamin A-types, the B-types represent major intermediate filaments of the nucleus and are involved in manifold interactions between the inner nuclear membrane and the the nuclear chromatin [33, 91]. The lamin proteins-based skeleton structure for formation of adaptor functions is important in chromatin organization and in modulation of signal transduction pathways. Minimal alterations in the chromatin structure can manifest clinical appearances [92, 93]. The extremely high organized chromatin architecture is pivotal in the strongly controlled gene expression. Dysregulations base on changes of the nuclear dis-organization and a disrupted nuclear structure is often noted in genetic diseases like cancer [94-96]. Studies of nuclear structure and activity using biophysical, chemical, and nanoscience methodologies under the aspect of problems, deriving from mutations and chromosome exchanges, in the genome organization demonstrate a sensitive connection to gene localization and activity [97-99].
Various groups indicated a non-random but highly organized structure of the genes as shown in Nicolini's, Harper's, Zink's and Cremers' research work [5, 11, 100-103].
Based on these above mentioned research results, we investigated which DNA sequences and genes in the nuclei were affected by light induced ROS. We constructed plasmids producing the KRED-lamin B1 fusion protein which is then located close to the nuclear inner surface (Supplementary Material: Figure 1a) and compared the damaged DNA sequences, with structures damaged by the activated recombinant H2A-KRED protein spatially scattered across the whole chromatin (Supplementary Material: Figure 1b).
The fact that ROS is capable to damage and finally kill cells is uncontradicted. These genotoxic and oxidative stress parameters damage DNA with double-strand breaks (DSBs), which then lead to an induction of DNA damage response (DDR).
In contrast to the lamin B1 induced break points, which can be interpreted to be very close to the nuclear shell, the histone H2A data cannot delineate gene positions and is our control.
We characterized especially genes with the highest damage rates induced by ROS, but not detected by histone H2A-KRED (Table 4 and Table 6 and Table 13a, Supplementary Material).
The strong increase of DNA damages from the lamina to the center of the nucleus supports the gradient of gene and chromosomes density in this direction.
Using independent triplicates of KRED-lamin B1 probes we detected the following damaged genes REXO1L2P, MLL2, LAMA5, and MUC12 with the nearly identical read count number (30 / 60 [min]) 6,824/6,039; 6,806/4,973; 5,420/3,793 and 4,688/4,544 respectively (Table 1). Chromatin dynamics and remodeling are required for the rapid DSB repair by mechanisms, highly conserved from yeast to humans as documented well from Price and Osley [104-106] .
Generally, the toxic potential of ROS depends on the distance from the point of its origin and is considered as assured. Here the differences in the parameters like absorption coefficients, spectral inhomogeneity of the incident light or in different ROS building capacities are not subject of our investigations.
Our data sets and especially the detected “fold change” data (Table 6) show a clear increase of the events of gene damage and indicate an enhancement of the density of the genes from the lamina inwards to the center of the nucleus as shown in Table 6.
The first 13 genes (listed in Table 4) offer the highest fold change factors between 371 and 103 in the lamin B1 probe but they are not measurable in the histone control. This suggests a localization near the lamin B1 protein at the inner surface of the nuclear envelope.
These results of the ROS cytotoxic effects, caused by both fusion proteins, the KRED-Lamin B1 variant as well as the histone H2A-KRED , demand further investigations of the local DNA characterization, chromosomal architecture and genotyping.
DNA of genes located at the nuclear periphery is generally a direct object for the insertion of viral DNA genomes and may promote formation of transcriptional activator complexes on the viral and cellular genome. The Silva (HPV) and the Marcello (HIV) groups demonstrated impressively, that the nuclear periphery also has sites for activation of transcription which highlights the importance of the nuclear lamina and the closely located genes in transcriptional activation and repression [107, 108].
Supplementary tables and figures
We thank the genomics and proteomics core facility group for support and Harald Hermann for the provided lamin B1 sequence.
On behalf of his retirement we like to thank Prof. Wolfhard Semmler for his enthusiasm, his inspiration, and his financial support for our work.
The authors have declared that no competing interest exists.
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Corresponding author: Dr. Klaus Braun, German Cancer Research Center (DKFZ), Dept. of Medical Physics in Radiology, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany. Phone: +49 6221-42 3329 Fax: +49 6221-42 3326 e-mail: k.braunde.