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  • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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  • C12Q2600/00—Oligonucleotides characterized by their use
  • C12Q2600/154—Methylation markers

Definitions

• the present invention relates to a method for diagnosing a cell with oxidative stress (OS).
• the method is capable of identifying OS in cell caused specifically by the cell’s exposure to Ultraviolet light and/or caused by ageing of the cell by determining differential methylation that takes place on CpG sites located on a particular gene body and the regulatory region of the specific gene.
• Oxidative stress refers to a serious imbalance between the levels of reactive oxygen species (ROS) in a cell and its antioxidant defense mechanism.
• ROS reactive oxygen species
• redox regulation to cope with the stress to maintain their homeostasis by regulating the redox state.
• This system functions to adapt to many external stress agents such as radiation, ultraviolet (UV) light rays, environmental pollutants, high fever, low temperature, hypoxic condition, and infectious diseases as well as to oxidative stress from lifestyle- related diseases such as cancer, diabetes, arteriosclerosis, hypertension and obesity.
• OS oxidative stress
• the human skin is constantly exposed to oxidative stress and free radicals, such as to high quantities of ROS, derived not only from ordinary metabolic reactions but also continuous exposure to air, radiation and UV rays, environmental pollutants, as well as physical and/or chemical agents (e.g., cosmetics). Under some conditions, the production of ROS may become so great that it may contribute to the pathogenesis of, for example, psoriasis or skin cancer. Oxidative damage caused by free radicals such as ROS is also a main cause of physical ageing in general, and of the skin in particular. Accordingly, there is a need in the art for detection of OS in cells, for example skin cells to prevent further damage to the cells.
• the present invention attempts to solve the problems above by providing a gene biomarker, differential methylation of which, is capable of being used for detecting OS in a cell. Since environmental factors/ agents such as, UV light exposure, ageing, diet and the like, may trigger OS which can further induce an alteration in the promoter CpG methylation status by recruiting DNA methyltransferases (DNMTs) and TET enzymes to various promoters, a biomarker resulting in differential methylation in a cell with OS is essential to overcome the problems mentioned above.
• the biomarker for detecting OS in a cell is differential methylation of a gene Protein Tyrosine Phosphatase Receptor Type N2 (PTPRN2).
• the CpGs of PTPRN2 in a cell with OS are differentially methylated (i.e. hypomethylated or hypermethylated) compared to the corresponding CpGs in a cell without OS.
• the CpGs of PTPRN2 are differentially methylated based on the source of OS. Accordingly, PTPRN2 may be effectively used to determine if a cell has OS. Different external agents can cause OS in a cell and the cell may have a different DNA methylation signature for each external agent causing OS.
• OS in a cell caused by UV light exposure and/or ageing may result in a specific group of CpGs that are differentially methylated compared to cells which do not have OS and/or cells which do not have OS caused by UV light exposure and/or ageing.
• the group of CpGs are one or more pre-selected CpG sites which are differentially methylated in cells with OS that is caused specifically by UV light exposure and/or ageing compared to cells with no OS or cells with OS caused by another external agent.
• an epigenetic marker is a long-term biomarker, that is to say it is inheritable and can be used to detect OS in the next generation as well if need be.
• a method of identifying oxidative stress (OS) caused by ageing and/or Ultraviolet (UV) light exposure in a test cell comprising
• the term "cell” refers to an intact live cell, naturally occurring or modified.
• the cell may be isolated from other cells, mixed with other cells in a culture, or within a tissue (partial or intact), or an organism.
• the cell may be a eukaryote cell.
• the cell may be mammalian cell.
• mammalian cell refers to any cell derived from a mammalian subject.
• the cell may also be a cell derived from the culture and expansion of a cell obtained from a subject.
• the cell may also have been genetically modified to express a recombinant protein and/or nucleic acid.
• the mammalian cell may be from humans and other primates, including nonhuman primates such as chimpanzees and other apes and monkey species; farm animals such as cattle, sheep, pigs, goats and horses; domestic mammals such as dogs and cats; rodents such as mice, rats, rabbits, hamsters, and guinea pigs; birds, including domestic, wild and game birds such as chickens, turkeys and other gallinaceous birds, ducks, geese, and the like.
• the subject is a mammal.
• the mammal is selected from the group consisting of a mouse, a rat, a guinea pig, a dog, a mini-pig, a human being, a cow, a sheep, a pig, a goat, a horse, a donkey, and a mule.
• the mammalian cell may be a skin cell, a stem cell or a cell derived therefrom. More in particular, the mammalian cell may be a skin cell.
• a “CpG site” or “methylation site” is a nucleotide within a nucleic acid (DNA or RNA) that is susceptible to methylation either by natural occurring events in vivo or by an event instituted to chemically methylate the nucleotide in vitro.
• a nucleic acid DNA or RNA
• the methylation status of at least one CpG site selected from the following list of 8 CpG sites in PTPRN2 is determined to determine if the cell has OS caused by ageing and/or UV light exposure:
• a “methylated nucleic acid molecule” refers to a nucleic acid molecule that contains one or more nucleotides that is/are methylated.
• a “CpG island” as used herein describes a segment of DNA sequence that comprises a functionally or structurally deviated CpG density.
• Yamada et al. have described a set of standards for determining a CpG island: it must be at least 400 nucleotides in length, has a greater than 50% GC content, and an OCF/ECF ratio greater than 0.6 (Yamada et al., 2004, Genome Research, 14, 247-266).
• Others have defined a CpG island less stringently as a sequence at least 200 nucleotides in length, having a greater than 50% GC content, and an OCF/ECF ratio greater than 0.6 (Takai et al., 2002, Proc. Natl.
• methylation profile “methylation pattern”, “methylation state” or “methylation status,” are used herein to describe the state, situation or condition of methylation of a genomic sequence, and such terms refer to the characteristics of a DNA segment at a particular genomic locus in relation to methylation. Such characteristics include, but are not limited to, whether any of the cytosine (C) residues within this DNA sequence are methylated, location of methylated C residue(s), percentage of methylated C at any particular stretch of residues, and allelic differences in methylation due to, e.g., difference in the origin of the alleles.
• C cytosine
• methylation status refers to the status of a specific methylation site (i.e. methylated vs. non-methylated) which means a residue or methylation site is methylated or not methylated. Then, based on the methylation status of one or more methylation sites, a methylation profile may be determined. Accordingly, the term “methylation profile” or also “methylation pattern” refers to the relative or absolute concentration of methylated C residues or unmethylated C residues at any particular stretch of residues in the genomic material of a biological sample.
• cytosine (C) residue(s) not typically methylated within a DNA sequence are methylated, it may be referred to as "hypermethylated”; whereas if cytosine (C) residue(s) typically methylated within a DNA sequence are not methylated, it may be referred to as "hypomethylated”.
• cytosine (C) residue(s) within a DNA sequence are methylated as compared to another sequence from a different region or from a different individual (e.g., relative to normal nucleic acid or to the standard nucleic acid of the reference sequence), that sequence is considered hypermethylated compared to the other sequence.
• the cytosine (C) residue(s) within a DNA sequence are not methylated as compared to another sequence from a different region or from a different individual, that sequence is considered hypomethylated compared to the other sequence.
• Measurement of the levels of differential methylation may be done by a variety of ways known to those skilled in the art.
• One method is to measure the methylation level of individual interrogated CpG sites determined by the bisulfite sequencing method, as a non-limiting example.
• a “methylated nucleotide” or a “methylated nucleotide base” refers to the presence of a methyl moiety on a nucleotide base, where the methyl moiety is usually not present in a recognized typical nucleotide base.
• cytosine in its usual form does not contain a methyl moiety on its pyrimidine ring, but 5-methylcytosine contains a methyl moiety at position 5 of its pyrimidine ring. Therefore, cytosine in its usual form may not be considered a methylated nucleotide and 5-methylcytosine may be considered a methylated nucleotide.
• thymine may contain a methyl moiety at position 5 of its pyrimidine ring, however, for purposes herein, thymine may not be considered a methylated nucleotide when present in DNA.
• Typical nucleotide bases for DNA are thymine, adenine, cytosine and guanine.
• Typical bases for RNA are uracil, adenine, cytosine and guanine.
• a "methylation site" is the location in the target gene nucleic acid region where methylation has the possibility of occurring. For example, a location containing CpG is a methylation site wherein the cytosine may or may not be methylated.
• methylated nucleotide refers to nucleotides that carry a methyl group attached to a position of a nucleotide that is accessible for methylation. These methylated nucleotides are usually found in nature and to date, methylated cytosine that occurs mostly in the context of the dinucleotide CpG, but also in the context of CpNpG- and CpNpN-sequences may be considered the most common. In principle, other naturally occurring nucleotides may also be methylated but they will not be taken into consideration with regard to any aspect of the present invention.
• methylation profile In context of the present invention, the terms “methylation profile”, “methylation pattern”, “methylation state” or “methylation status,” are used herein to describe the state, situation or condition of methylation of a genomic sequence, and such terms refer to the characteristics of a DNA segment at a particular genomic locus in relation to methylation. Such characteristics include, but are not limited to, whether any of the cytosine (C) residues within this DNA sequence are methylated, location of methylated C residue(s), percentage of methylated C at any particular stretch of residues, and allelic differences in methylation due to, e.g., difference in the origin of the alleles.
• C cytosine
• hypomethylation refers to the average methylation state corresponding to an increased presence of 5-mCyt at one or a plurality of CpG dinucleotides within a DNA sequence of a test DNA sample, relative to the amount of 5-mCyt found at corresponding CpG dinucleotides within a normal control DNA sample.
• control refers to a cell with no indication of OS.
• hypomethylation refers to the average methylation state corresponding to a decreased presence of 5-mCyt at one or a plurality of CpG dinucleotides within a DNA sequence of a test DNA sample, relative to the amount of 5-mCyt found at corresponding CpG dinucleotides within a normal control DNA sample.
• control refers to a cell with no indication of OS.
• gene refers to the respective genomic DNA sequence, including any promoter and regulatory sequences of the gene (e.g., enhancers and other gene sequences involved in regulating expression of the gene), and/or the body of the gene in itself.
• a gene sequence may be an expressed sequence (e.g., expressed RNA, mRNA, cDNA). Further, where SNPs are known within genes the term shall be taken to include all sequence variants thereof.
• genomic material refers to nucleic acid molecules or fragments of the genome of the subject or group of subjects.
• nucleic acid molecules or fragments are DNA or RNA or hybrids thereof, and most preferably are molecules of the DNA genome of a subject or group of subjects.
• promoter or “gene promoter” used interchangeably with the term ‘regulatory region’ or ‘regulatory sequence’ refers to the respective contiguous gene DNA sequence extending from 1 .5 kb upstream to 1 .5 kb downstream relative to the transcription start site (TSS), or contiguous portions thereof.
• regulatory region refers to the respective contiguous gene DNA sequence extending from 1 .5 kb upstream to 0.5 kb downstream relative to the TSS.
• ‘regulatory region’ refers to the respective contiguous gene DNA sequence extending from 1 .5 kb upstream to the downstream edge of a CpG island that overlaps with the region from 1 .5 kb upstream to 1 .5 kb downstream from TSS (and is such cases, my thus extend even further beyond 1 .5 kb downstream), and contiguous portions thereof.
• any CpG dinucleotide of the gene that is coordinately methylated with the ‘regulatory region’ of the gene has substantial diagnostic/classification utility as disclosed herein.
• the “DNA sample” refers to the DNA extracted from the cell according to any aspect of the present invention using known methods in the art.
• the test cell when there is differential methylation detected in a test cell, that is to say that the cell displays hypermethylation or hypomethylation at, at least one CpG site in comparison to the control (i.e., a cell without indication of OS), then the test cell has OS.
• the test cell when there is differential methylation detected in one of the 8 specific CpG sites listed above in Table 1 , that is to say that the cell displays hypermethylation or hypomethylation at, at least one CpG site from the list of 8 CpG sites in Table 1 comparison to the control (i.e., a cell without indication of OS or a cell with indication of OS cause by an external factor other than UV light exposure and/or ageing), then the test cell has OS caused by UV light exposure and/or ageing.
• the control i.e., a cell without indication of OS or a cell with indication of OS cause by an external factor other than UV light exposure and/or ageing
• step (a) the methylation status of at least at least 2, 3, 4, 5, 6, 7, or 8 CpG sites from Table 1 in PTPRN2 are determined.
• the method according to any aspect of the present invention may further comprise the step of:
• ‘Bisulfite treatment’ of genomic DNA used interchangeably with the term ‘bisulfite modification’ refers to the treatment of the genomic DNA with a deaminating agent such as a bisulfite that may be used to treat all DNA, methylated or not.
• a deaminating agent such as a bisulfite that may be used to treat all DNA, methylated or not.
• bisulfite as used herein encompasses any suitable type of bisulfite, such as sodium bisulfite, or other chemical agents that are capable of chemically converting a cytosine (C) to an uracil (U) without chemically modifying a methylated cytosine and therefore can be used to differentially modify a DNA sequence based on the methylation status of the DNA, e.g., U.S. Pat. Pub. US 2010/0112595.
• a reagent that "differentially modifies" methylated or non-methylated DNA encompasses any reagent that modifies methylated and/or unmethylated DNA in a process through which distinguishable products result from methylated and non-methylated DNA, thereby allowing the identification of the DNA methylation status.
• processes may include, but are not limited to, chemical reactions (such as a C to U conversion by bisulfite) and enzymatic treatment (such as cleavage by a methylation-dependent endonuclease).
• an enzyme that preferentially cleaves or digests methylated DNA is one capable of cleaving or digesting a DNA molecule at a much higher efficiency when the DNA is methylated, whereas an enzyme that preferentially cleaves or digests unmethylated DNA exhibits a significantly higher efficiency when the DNA is not methylated.
• step (a) the genomic DNA contained/ obtained or extracted from the cell, is first bisulfite treated.
• TET-assisted pyridine borane sequencing may be used for detection of 5mC and 5hmC (Yibin Liu, et al., Nature Biotechnology, 37: 424-429 (2019).
• the cell used according to any aspect of the present invention is obtained from a biological sample selected from the group consisting of blood, brain, sperm and any other tissue or sample that provides genomic DNA to be used in the method according to any aspect of the present invention.
• the biological sample may comprise any biological material obtained from the subject that contains DNA, and may be liquid, solid or both, may be tissue or bone, or a body fluid such as blood, lymph, etc.
• the biological sample useful for the present invention may comprise biological cells or fragments thereof.
• test used in conjunction with the term cell herein refers to a cell that is subjected to the method according to any aspect of the present invention and is the basis for an analysis application of the present invention.
• a ‘test cell’ is therefore a cell or a group of cells being tested according to any aspect of the present invention or a profile being obtained or generated in this context.
• reference shall denote, mostly predetermined, entities which are used for a comparison with the test entity.
• a ‘test cell’ refers to a cell being tested for OS where the methylation status has to be determined and a ‘control’ refers to a cell without OS where the methylation status is already known and used as a reference.
• a method of identifying oxidative stress (OS) caused by ageing and/or Ultraviolet (UV) light exposure in at least one cell comprising detecting a difference in expression of Protein Tyrosine Phosphatase Receptor Type N2 (PTPRN2).
• OS oxidative stress
• UV Ultraviolet
• epigenetic marker refers to a gene in itself and/or CpG sites of the gene body and/or CpG sites of the regulatory region of the gene, that comprises epigenetic modifications, wherein the epigenetic modifications enable the gene to be used as a marker to determine a particular disease.
• the term “epigenetic marker” is defined as at least one of a DNA methylation marker, a histone modification marker, and a deacetylase marker.
• the epigenetic marker for OS caused by ageing and/or Ultraviolet (UV) light exposure in a cell is the differential methylation that is found in the CpG sites on the gene body and/or regulatory region of PTPRN2.
• the epigenetic marker for OS caused by ageing and/ or UV light exposure is the differential methylation of the 8CpG sites in Table 1 above which are found in the gene body and/or regulatory region of PTPRN2 in the cell with OS caused by ageing and/ or UV light exposure relative to the control cell with no OS or with OS caused by another external factor other than ageing and/ or UV light exposure.
• promoter-specific hyper/hypomethylation leads to changes in the expression of different genes.
• the differential methylation of the CpG sites in PTPRN2 results in the differential expression of PTPRN2.
• This differential expression of the gene relative to a control, where there is no differential methylation, is indicative of OS, particularly, that caused by ageing and/ or UV light exposure in the cell tested.
• hypermethylation of the promoter is associated with the inactivation of gene expression of PTPRN2.
• hypomethylation of the promoter is associated with the (over)activation of gene expression of PTPRN2.
• Figure 1 is a graph showing the number of probes that were differentially methylated in different gene bodies and promoter regions of cells where artificial OS (high UV light for 24hrs) was induced according to Example 1 .
• genes, MAD1L1 (meiotic spindle arrest component) and PTPRN2 similar to receptor-like protein tyrosine phosphatases have the highest differentially methylated probe distribution.
• the other genes which were also differentially methylated in a cell with OS are shown.
• Figure 2 is a graph showing the number of probes that were differentially methylated in different gene bodies and promoter regions of cells artificial OS (low UV light for 72hrs) was induced according to Example 1 .
• genes, MAD1L1 (meiotic spindle arrest component) and PTPRN2 (similar to receptor-like protein tyrosine phosphatases) have the highest differentially methylated probe distribution.
• the other genes which were also differentially methylated in a cell with OS are shown.
• Figure 3 is a graph showing the number of probes that were differentially methylated in different gene bodies and promoter regions of cells where artificial OS (high H2O2 for 24hrs) was induced according to Example 2.
• genes, MAD1L1 (meiotic spindle arrest component) and PTPRN2 similar to receptor-like protein tyrosine phosphatases have the highest differentially methylated probe distribution.
• the other genes which were also differentially methylated in a cell with OS are shown.
• Figure 4 is a graph showing the number of probes that were differentially methylated in different gene bodies and promoter regions of cells artificial OS (low H2O2 for 24hrs) was induced according to Example 2.
• genes, MAD1L1 (meiotic spindle arrest component) and PTPRN2 similar to receptor-like protein tyrosine phosphatases have the highest differentially methylated probe distribution.
• the other genes which were also differentially methylated in a cell with OS are shown.
• Figure 5 is a graph showing the number of probes that were differentially methylated in different gene bodies and promoter regions of cells where artificial OS according to Example 3 with Medox ® in cells was induced.
• genes, MAD1L1 (meiotic spindle arrest component) and PTPRN2 (similar to receptor-like protein tyrosine phosphatases) have the highest differentially methylated probe distribution.
• the other genes which were also differentially methylated in a cell with OS are shown.
• Figure 6 is a graph showing the Top 20 overlapping genes at different treatments related to UV light exposure and ageing.
• T-Skin models were obtained from Episkin SA, France which is composed of reconstructed human skin. Each skin model consists of a dermal equivalent overlaid by a stratified, well-differentiated epidermis derived from normal human keratinocytes. Upon receiving the skin models, it was recovered by incubating in T-Skin culture medium overnight at 37°C in a 5% CO2 incubator.
• the genomic DNA (500ng) from tissue samples were subjected to bisulfite conversion using the EZ DNA Methylation-GoldTM Kit (Zymo Research).
• the methylation levels were quantified using Infinium MethylationEPIC v2.0 Kit (Illumina) which can analyze over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
• Methylation EPIC array data processing was performed in R version 4.1 .2 (2021-11-01) using the minfi version 1 .40.0.
• the raw intensity data (IDAT) were imported into the R (4.1 .2), processed using the minfi (1 .4.0) Bioconductor packaged 8.
• Quality check on samples was performed to keep probes that have a detection P-value ⁇ 0.01 in one or more samples or have a mean detection P- value ⁇ 0.05 in all samples. Then samples were normalized using functional normalization (implemented by preprocessFunnorm function in minfi) for type-bias correction and background correction.
• the probes with non-specific binding, cross reactive probes, probes affected by common SNPs, and probes annotated to the X,Y chromosomes were also filtered out.
• Beta-value and M-value of normalized and filtered samples were calculated using getBeta and getM function respectively, the samples were then subjected to further downstream analysis.
• Differential methylation analysis was performed using packages limma version 3.50.1 and DMRcate version 2.8.5. Contrast matrix was set up by comparing each corresponding treatment and control group and empirical Bayesian algorithm was used to fit the M-values based on the design and contrast model. Probes with adjusted P-value lower than 0.05 were considered as differentially methylation positions (DMPs). Annotation was performed using HluminaHumanMethylationEPICkanno.ilmn12.hg19 and annotatr package (1 .20.0).
• PTPRN2 Protein Tyrosine Phosphatase Receptor Type N2
• PTPRN2 is phosphatidylinositol phosphatase with the ability to dephosphorylate phosphatidylinositol 3-phosphate and phosphatidylinositol 4,5-diphosphate which plays important roles in lipid signaling, cell signaling and membrane trafficking.
• Example 2 Same method of quality control and data processing as that disclosed in Example 1 was carried out on the samples here. Further, the same differential methylation analysis as disclosed in Example 1 was carried out on the data obtained from Example 2.
• MSCs Mesenchymal Stem Cells
• Medox® Evonik, Batch:H-080719
• Bone marrow derived MSCs were cultured for 1 week in Mesencult ACF Plus Medium with two doses of Medox® (4x replicates): 25 pg/ml (low) and 100 pg/ml (high). The media with Medox® was replaced every second day for 1 week.
• Medox® treatment is expected to produce the opposite reaction to OS.
• genomic DNA was quantified using the PicroGreen® or NanoDropTM 2000.
• the genomic DNA (500ng) from the cell pellet was subjected to bisulfite conversion using the EZ DNA Methylation-GoldTM Kit (Zymo Research).
• the methylation levels were quantified using Infinium MethylationEPIC v2.0 Kit (Illumina) which can analyze over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
• DNA methylation profiling has been proven to be a powerful analytical tool to accurately identify the origin of tissue and the effect of environmental factors. It has several advantages as a biomarker classifier as it is a stable marker, and it can facilitate quantitative analysis at single-nucleotide resolution.
• Example 3 Same method of Quality control and data processing as that disclosed in Example 1 was carried out on the samples here. Further, the same differential methylation analysis as disclosed in Example 1 was carried out on the data obtained from Example 3.
• PTPRN2 Protein Tyrosine Phosphatase Receptor Type N2
• PTPRN2 is phosphatidylinositol phosphatase with the ability to dephosphorylate phosphatidylinositol 3-phosphate and phosphatidylinositol 4,5-diphosphate which plays important roles in lipid signaling, cell signaling and membrane trafficking.
• the skin models were maintained in the deep well plate with media for 7 days (4x replicates), 14 days (4x replicates) and 21 days (4x replicates) respectively to induce ageing in the skin tissue.
• a control set of skin models (4x replicates) were collected at Ohr for genomic DNA isolation. Skin models were collected after 7 days, 14 days and 21 days respectively, and genomic DNA was purified from the tissue samples using the DNeasy® Blood & Tissue Kit (Qiagen). The genomic DNA was quantified using the PicroGreen® or NanoDropTM 2000.
• the genomic DNA (500ng) from tissue samples were subjected to bisulfite conversion using the EZ DNA Methylation-GoldTM Kit (Zymo Research).
• the methylation levels were quantified using Infinium MethylationEPIC v2.0 Kit (Illumina) which can analyze over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
• UV radiation UVA 24 J/cm 2 + UVB 50mJ/cm 2
• skin models were exposed to UV radiation (UVA 24 J/cm 2 + UVB 50mJ/cm 2 ) daily and cultured for 24 hrs (4x replicates), 48 hrs (4x replicates), 72hrs (4x replicates), 96hrs (4x replicates) and 120hrs (4x replicates) respectively.
• a control set of skin models were maintained for 24 hrs (4x replicates), 48 hrs (4x replicates), 72hrs (4x replicates), 96hrs (4x replicates) and 120hrs (4x replicates) respectively without any exposure to UV radiation.
• skin models were collected, and genomic DNA was purified from the tissue samples using the DNeasy® Blood & Tissue Kit (Qiagen). The genomic DNA was quantified using the PicroGreen® or NanoDropTM 2000.
• the genomic DNA (500ng) from tissue samples were subjected to bisulfite conversion using the EZ DNA Methylation-GoldTM Kit (Zymo Research).
• the methylation levels were quantified using Infinium MethylationEPIC v2.0 Kit (Illumina) which can analyze over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
• the probes with non-specific binding, cross reactive probes, probes affected by common SNPs, and probes annotated to the X,Y chromosomes were also filtered out.
• Beta-value and M-value of normalized and filtered samples were calculated using getBeta and getM function respectively, the samples were then subjected to further downstream analysis.
• Pair-wise differential methylation analysis (total of 7 pairs) was performed using the limma package version 3.52.4. The UV samples and Aged samples were analyzed separately. Contrast matrix was set up by comparing each corresponding treatment and control group and empirical Bayesian algorithm was used to fit the M-values based on the design and contrast model. Probes with adjusted P-value lower than 0.05 were considered as differentially methylation positions (DMPs). Annotation was performed using HluminaHumanMethylationEPICanno.ilm10b2.hg19. Genes that overlapped at all treatments were then found and their DMPs were analyzed to identify DMPs that were present in all comparisons.
• PTPRN2 Protein Tyrosine Phosphatase Receptor Type N2
• PTPRN2 is phosphatidylinositol phosphatase with the ability to dephosphorylate phosphatidylinositol 3-phosphate and phosphatidylinositol 4,5-diphosphate which plays important roles in lipid signaling, cell signaling and membrane trafficking.
• PTPRN2 gene had a total of 670 unique DMPs, of which 8 DMPs were seen in all comparisons (Table 3).
• Table 3 8 DMPs of PTPRN2 that were common between all treatments and their methylation status at each treatment.

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• 2023
  • 2023-04-21 WO PCT/EP2023/060484 patent/WO2023213573A1/en not_active Ceased
  • 2023-04-21 JP JP2024564840A patent/JP2025514485A/ja active Pending
  • 2023-04-21 KR KR1020247039681A patent/KR20250004022A/ko active Pending
  • 2023-04-21 CA CA3251480A patent/CA3251480A1/en active Pending
  • 2023-04-21 US US18/861,274 patent/US20250290141A1/en active Pending
  • 2023-04-21 CN CN202380038053.XA patent/CN119137288A/zh active Pending
  • 2023-04-21 EP EP23721662.7A patent/EP4519458B1/en active Active
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