{"id":7637,"date":"2015-06-09T12:32:33","date_gmt":"2015-06-09T11:32:33","guid":{"rendered":"http:\/\/www.wjst.de\/blog\/?p=7637"},"modified":"2015-06-19T08:42:59","modified_gmt":"2015-06-19T07:42:59","slug":"5-of-methylated-sites-escape-reprogramming-a-new-allergy-research-direction","status":"publish","type":"post","link":"https:\/\/www.wjst.de\/blog\/sciencesurf\/2015\/06\/5-of-methylated-sites-escape-reprogramming-a-new-allergy-research-direction\/","title":{"rendered":"5% of methylated sites escape reprogramming &#8211; a new allergy research direction"},"content":{"rendered":"<p>New Scientist Health has a short report <a href=\"http:\/\/www.newscientist.com\/article\/dn27658-first-evidence-of-how-parents-lives-could-change-childrens-dna.html?cmpid=RSS|NSNS|2012-GLOBAL|life#.VXbIVmDARQk\">how parents&#8217; lives could change children&#8217;s DNA<\/a>.<\/p>\n<blockquote><p>Azim Surani at Cambridge University and colleagues have demonstrated that some genes in the developing fetus escape the cleaning mechanism.\u00a0Surani&#8217;s team analysed methylation patterns in a type of fetal cell that later forms a fetus&#8217;s own sperm or eggs. We would expect these cells to have been wiped clean when the fetus&#8217;s epigenome was reset at the early embryo stage. &#8220;However, about 2 to 5 per cent of methylation across the genome escaped this reprogramming,&#8221; says Surani.<\/p><\/blockquote>\n<p>The current wave of interest stems from\u00a0three new papers:\u00a0&#8220;<a href=\"http:\/\/www.cell.com\/cell\/abstract\/S0092-8674(15)00563-2\">The Transcriptome and DNA Methylome Landscapes of Human Primordial Germ Cells<\/a>&#8221; by Guo demonstrates<\/p>\n<blockquote><p>The transcriptome of human primordial germ cells from the migrating stage to the gonadal stage reveals that both pluripotency genes and germline-specific genes are simultaneously expressed within the same individual cells. The global erasure of DNA methylation creates a super-hypomethylated germline genome.<\/p><\/blockquote>\n<p>So at week 10 after gestation, all\u00a0analyzed 233\u00a0\u00a0primordial germ cells lost their parental methylation marks except of 6% of the male and 8% of the female genome (which is a bit larger) . Unfortunately I did not find a\u00a0list of genes there that have their parental methylation status transmitted.<\/p>\n<p>Tang from a\u00a0British consortium\u00a0&#8220;<a href=\"http:\/\/www.cell.com\/cell\/abstract\/S0092-8674(15)00564-4\">A Unique Gene Regulatory Network Resets the Human Germline Epigenome for Development<\/a>&#8221; writes<\/p>\n<blockquote><p>A unique transcriptome drives extensive epigenome resetting in human primordial germ cells for establishment of totipotency. Some loci associated with metabolic and neurological disorders exhibit resistance to reprogramming and are candidates for transgenerational epigenetic inheritance.<\/p><\/blockquote>\n<p>Here evolutionarily young and potentially hazardous retroelements, like SVA, remain methylated ( the number of embryos \u00a0being examined is not given). Evolutionarily young and potentially hazardous retroelements, like SVA, remain methylated.\u00a0When testing for resistant loci, they\u00a0found that H3K9me3 marked escaping ; resistant regions were also enriched for KAP1 (alias TRIM28) binding sites of ESCs. But still no gene list there.<\/p>\n<p>Sofia Gkountela &#8220;<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0092867415005632\">DNA Demethylation Dynamics in the Human Prenatal Germline<\/a>&#8221; from the US<\/p>\n<blockquote><p>performed whole-genome bisulfite sequencing (WGBS) and RNA-sequencing (RNA-seq) of human prenatal germline cells from 53 to 137 days of development. We discovered that the transcriptome and methylome of human germ-line is distinct from both human PSCs and the inner cell mass (ICM) of human blastocysts &#8230; Gene expression do not correlate with global changes in DNA methylation.<\/p><\/blockquote>\n<p>In this paper finally there is\u00a0the gene list, I was looking for &#8212; basically\u00a0not demethylated, parentally inherited genes.\u00a0Persistent\u00a0methylated regions (also termed DMR, differential methylated regions) in advanced germline cells (AGCs) were seen in 500+\u00a0genes as given in\u00a0table S4:<\/p>\n<blockquote><p>AADACL2-AS1, ABCA7, ABCC5, ABHD12, ABR, AC093375.1, ACSL4, ACSM1, ACVR1C, ACYP1, ADAMTSL3, ADARB2, ADK, AGBL4, AGK, AGPS, AIG1, AKAP9, AKR1B15, ALPK2, ANK1, ANKHD1, ANKHD1-EIF4EBP3, ANKRD11, ANKRD12, ANKRD19P, ANKRD20A9P, ANKRD24, ANKRD26, ANKRD26P1, ANKRD30BL, ANKRD31, AP2A2, AP3D1, AP4E1, ARAP2, ARHGAP26, ARHGAP39, ARHGAP44, ARHGEF18, ARHGEF4, ARHGEF7, ARID3A, ARL13B, ASB3, ASH1L, ASTN2, ASZ1, ATAD3A, ATF1, ATP11A, ATP13A1, ATP2C1, ATP8A2, ATP9B, AUH, AVEN, BAGE, BAGE2, BAGE3, BAGE4, BAGE5, BASP1P1, BAZ1A, BBS9, BCAS3, BCO2, BCYRN1, BEND3, BEND7, BRE, BRSK2, C14orf159, C15orf37, C1GALT1, C1orf159, C20orf196, C22orf34, C2orf61, C3orf67, C3orf67-AS1, C7orf50, C7orf60, C9orf3, CACNA1B, CACNG4, CALN1, CAMK1D, CARF, CARS2, CC2D2A, CCBL2, CCDC101, CCDC130, CCDC148, CCDC149, CCDC57, CCDC88C, CCDC97, CCNY, CCSER1, CD163, CD2AP, <strong>CD46<\/strong>, CDH12, CDH4, CDKAL1, CELF2, CEP70, CERK, CERS4, CFH, CHD2, CHD6, CHODL, CHRM5, CHRNA10, CHRNA4, CLEC16A, CLIC5, CLIC6, CNOT2, CNTN6, CNTNAP2, COG2, <strong>COL15A1<\/strong>, COL18A1, COL24A1, COL6A4P2, COLEC11, CORO2B, CPVL, CRTC3, CSMD1, CSMD2, CSNK1D, CTB-7E3.1, CTDP1, CTIF, CTNNA2, CTNNA3, CUBN, CXCR2, CXorf49, CXorf49B, CYCS, CYP3A5, DAPK2, DCDC2C, DDA1, DENND1A, DENND5A, DGUOK-AS1, DIP2C, DLG1, DLK1, DNAH6, DNAH8, DNAJC1, DNER, DOC2GP, DOCK1, DOCK7, DPP10, DSTN, DTNB, DYX1C1, DYX1C1-CCPG1, EBF3, ECHDC2, EDIL3, EEPD1, EFCAB10, EFCAB4B, EFTUD1, EHBP1, EIF2B3, ELMO1, EP400NL, EPHA6, EPPK1, ERC1, ERCC8, ERICH1-AS1, ERP44, ETFA, EVC2, EXD3, EXOC2, EYS, F11-AS1, FAAH, FAM172A, FAM174A, FAM207A, FAM209A, FAM86FP, FANCC, FBN3, FBXO39, FGD4, FGF14, FHIT, FIG4, FLJ30403, FNBP4, FOXN3, FREM3, FZR1, GABRA2, GAS6, GBP2, GCNT7, GDA, GGCX, GLCCI1, GLRA1, GLRA2, GMDS, GNAI1, GOLIM4, GPR75-ASB3, GRIK2, GRM7, GTF3C6, GTPBP10, GUSBP1, H6PD, HCCAT3, HCN4, HDAC4, HECTD4, HEG1, HPGD, HRNR, HS6ST3, HTR7, IFNAR1, IGF2BP3, IGSF11, IGSF22, IGSF9B, IL1RAPL2, IL31RA, IMMP2L, IMPG2, INF2, INTS1, INVS, IPO7, IQCF3, IQCG, <strong>IRAK1BP1<\/strong>, ISOC2, ISPD, ITFG1, ITGB1BP2, ITGBL1, JAM3, JAZF1, JMJD1C, KALRN, KATNBL1, KDM3B, KDM4C, KIAA0825, KIAA1328, KIF4A, KIF5B, KLHL20, KLHL3, LANCL3, LDB2, LDLRAD3, LHCGR, LINC00239, LINC00408, LINC00469, LINC00670, LINC00871, LINC00922, LINC01193, LINC01194, LINGO2, LMF1, LOC100128505, LOC100133669, LOC100188947, LOC100289333, LOC101927069, LOC101927280, LOC101927286, LOC101929064, LOC101929387, LOC102723742, LOC145837, LOC283683, LOC285768, LOC286083, LOC442132, LPA, LPPR1, LRP1B, LRRC4C, LTBP1, LUZP2, MAD1L1, MAGT1, MAML3, MAOA, MAP3K15, MAP4K5, MAPK10, MAPK8, MAPK8IP3, MAST2, MCTP1, MCU, MEF2A, MEI4, MELK, METTL15, METTL9, MFHAS1, MIR1273H, MIR518B, MIR518F, MIR520B, MIR548H2, MIR548O2, MIR6130, MIR6744, MOB3B, MOCOS, MTG1, MTMR7, MUC2, MUC5B, MUM1L1, MYO10, MYO5A, MYO9A, MYT1, MYT1L, NAA20, NAALADL2, NAT1, NAV2, NBPF10, NBPF20, NCALD, NCOA2, NEBL, NFATC3, NIFK-AS1, NIPA1, NKAIN2, NKAIN3, NLRP4, NME7, NOC4L, NONO, NPHP4, NQO2, NRXN3, NSUN6, NTSR1, NUBPL, NXN, OGG1, OR8S1, OSBP2, OSBPL6, OSMR, PACS2, PARK2, PARL, PAWR, PCBP3, PCDH19, PCDH9, PCNT, PCNXL2, PCSK6, PDAP1, PDE11A, PDE4D, PGAM1P5, PGAM5, PHKB, PHRF1, PIK3C2A, PIK3CA, PIP5K1B, PKD2L1, PKHD1, PKIB, PLCD1, PLCH1, PLEC, PLOD2, POLR1A, POMK, PPARA, PPARGC1B, PPP2R5C, PRH1, PRH1-PRR4, PRICKLE1, PRKAR1B, PRKCZ, PROSER2, PROSER2-AS1, PRR26, PRUNE2, PTCD3, PTDSS2, PTGFRN, PTPN21, PTPRD, PTPRN2, PYGB, RAB28, RAB3D, RAB3GAP2, RAB3IP, RABGAP1L, RAPGEF6, RBFOX1, RC3H2, RFX7, RGS6, RGS7, RNF115, RNH1, RNU6-52P, RNU6-81P, RPH3AL, RPIA, RPL35A, RPS6KC1, RSPH1, RYR1, S100Z, SCAPER, SCCPDH, SCEL, SCFD2, SCHLAP1, SCMH1, SDHAP3, SDK1, SEC14L1, SEC24D, SEL1L, SEMA3C, SERPINB3, SESN2, SESTD1, SETD1A, SETDB1, SHANK2, SHC2, SIL1, SIN3B, SLC12A3, SLC22A15, SLC24A2, SLC38A10, SLC44A5, SLC6A1, SLC8A1-AS1, SNORD115-1, SNORD115-2, SNTB2, SNTG2, SNX29, SORCS2, SOX5, SPATA5, SPIDR, SPIRE1, SPTB, SPTBN2, SPTLC3, SRD5A1, SRRM4, ST20, ST20-MTHFS, ST6GAL1, STARD9, <strong>STIM1<\/strong>, STK31, STK38, STON1-GTF2A1L, STXBP5-AS1, SUPT3H, SYN3, TAF1L, TAS2R19, TENM2, TENM3, THRB, THSD7B, TIMM23B, TJP2, TLK1, TMCC1, TMED1, TMEM132D, TMEM218, TMEM66, TMTC2, TNRC6B, TPST1, TPTE, TRAPPC9, TRIO, TRPC4AP, TRPM2, TRRAP, TSNARE1, TSPAN15, TSPEAR, TSSC1, TTC28, TTC40, TULP4, TYRO3P, TYSND1, TYW1B, UGGT2, UHRF1, ULK4, UNC5D, UNC79, UNC93A, USP13, USP15, USP34, USP50, VGLL4, VPRBP, VPS53, WDPCP, WDR1, WDR19, <strong>WDR36<\/strong>, WDR60, WWOX, XAF1, ZBTB20, ZCWPW2, ZFPM2, ZFYVE9, ZKSCAN5, ZMAT1, ZMYM4, ZNF135, ZNF14, ZNF317, ZNF32, ZNF32-AS1, ZNF32-AS2, ZNF32-AS3, ZNF335, ZNF341, ZNF350, ZNF382, ZNF415, ZNF556, ZNF595, ZNF664-FAM101A, ZNF670, ZNF670-ZNF695, ZNF7, ZNF717, ZNF718, ZNF767P, ZNF808, ZNF845, ZNRF1, ZSWIM5<\/p><\/blockquote>\n<p>(I dropped two genes as they are only\u00a0date-formatted numbers in the supplied Excel sheet).<\/p>\n<p>The interesting question\u00a0for me is if there is an\u00a0interaction with genes identified earlier in asthma and allergy research. According to the GWAS catalog there are 190 associated genes\u00a0that match\u00a0only 9\u00a0on the list above: AS1, CLEC16A, CTNNA3, EDIL3, PDE4D, PGAM1P5, SDK1, WDR36.\u00a0Nothing exciting, in particular no HLA association. WDR36 is the only gene, <a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/19198610\">we published <\/a>some years ago. I find also\u00a0only one match (COL15A1) of the <a href=\"http:\/\/www.nature.com\/nature\/journal\/v520\/n7549\/abs\/nature14125.html\">73 low methylation IgE loci<\/a>\u00a0published earlier.<\/p>\n<p>Possibly, any of these persistent methylated genes can even stand on its\u00a0own feet with just one silenced \/ activated gene \u00a0being responsible for the\u00a0pathology in a\u00a0pedigree. I cannot identify so many signals in the list above, maybe some IL1 related stuff (IL1RAPL2, IL31RA, IRAK1BP1).\u00a0CD46 at least is\u00a0a good candidate\u00a0<a href=\"http:\/\/www.jacionline.org\/article\/S0091-6749(14)00810-0\/abstract\">as it is known<\/a> that enhanced CD46-induced regulatory T cells will suppress allergic inflammation after allergen specific immunotherapy.<\/p>\n<p>Unexpectedly, there are\u00a0also no vitamin D related genes, no VDR, no\u00a0cytochrome P450 enzymes. Nevertheless I recognize a whole bunch of calcium related genes: \u00a0STIM1 (transmembrane protein that mediates Ca2+ influx), \u00a0ATP11A + ATP2C1\u00a0(ATP dependent Ca2+ transporter),\u00a0TRPM2 ( another Ca2+ channel), TRPC4AP + RYR1 (sarcoplasmic reticulum calcium channels) and NCALD (a cytosolic calcium transporter).<\/p>\n<p>So would be definitely interesting to test the methylation status of these genes along with vitamin D levels in allergic parents and their kids.<\/p>\n\n<p>&nbsp;<\/p>\n<div class=\"bottom-note\">\n  <span class=\"mod1\">CC-BY-NC Science Surf , accessed 07.05.2026<\/span>\n <\/div>","protected":false},"excerpt":{"rendered":"<p>New Scientist Health has a short report how parents&#8217; lives could change children&#8217;s DNA. Azim Surani at Cambridge University and colleagues have demonstrated that some genes in the developing fetus escape the cleaning mechanism.\u00a0Surani&#8217;s team analysed methylation patterns in a type of fetal cell that later forms a fetus&#8217;s own sperm or eggs. We would &hellip; <a href=\"https:\/\/www.wjst.de\/blog\/sciencesurf\/2015\/06\/5-of-methylated-sites-escape-reprogramming-a-new-allergy-research-direction\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">5% of methylated sites escape reprogramming &#8211; a new allergy research direction<\/span> <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8,2,10],"tags":[2942,2939,2938,2618,1944,2941,287,2940,1287],"class_list":["post-7637","post","type-post","status-publish","format-standard","hentry","category-asthma-allergy","category-genetics-biology","category-sunshine-vitamin","tag-dohad","tag-kammerer","tag-waddington","tag-calcium","tag-calcium-supplementation","tag-early-priming","tag-epigenetics","tag-vitamin-d-deficiency","tag-vitamin-d"],"_links":{"self":[{"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/posts\/7637","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/comments?post=7637"}],"version-history":[{"count":16,"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/posts\/7637\/revisions"}],"predecessor-version":[{"id":7672,"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/posts\/7637\/revisions\/7672"}],"wp:attachment":[{"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/media?parent=7637"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/categories?post=7637"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.wjst.de\/blog\/wp-json\/wp\/v2\/tags?post=7637"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}