Vassilios Alexiadis , Mary E. Ballestas , Cecilia Sanchez , Sara Winokur , Vettaikorumakankav Vedanarayanan , Mary Warren , Melanie Ehrlich
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By RNAPol-ChIP and RT-PCR, little or no transcription of D4Z4 was detected in FSHD and normal myoblasts; lymphoblasts from an FSHD patient, a control, and a patient with D4Z4 hypomethylation due to mutation of DNMT3B (ICF syndrome); and normal or cancer tissues. However, RNAPol-ChIP assays indicated transcription of D4Z4 in a chromosome 4-containing human–mouse somatic cell hybrid. ChIP and RT-PCR showed satellite DNA transcription in some cancers and lymphoblastoid cell lines, although only at a low level. Given the evidence for the involvement of RNAi in satellite DNA heterochromatinization, it is surprising that, at most, a very small fraction of satellite DNA was associated with RNA Pol II. In addition, our results do not support the previously hypothesized disease-linked differential transcription of D4Z4 sequences in short, FSHD-linked arrays.</p></div>","PeriodicalId":100161,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression","volume":"1769 1","pages":"Pages 29-40"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bbaexp.2006.11.006","citationCount":"67","resultStr":"{\"title\":\"RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA\",\"authors\":\"Vassilios Alexiadis , Mary E. 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引用次数: 67
摘要
RNA干扰(RNAi)涉及维持串联DNA阵列作为组成性异染色质。我们使用RNA聚合酶II抗体的染色质免疫沉淀法(RNA - chip)检测了人类细胞中以下重复序列的转录:亚端粒D4Z4、周着丝粒卫星2和着丝粒卫星α。D4Z4在其3.3 kb重复单元的ORF上游有一个类似启动子的序列。位于4q35的短D4Z4序列与面肩肱骨肌营养不良症(FSHD)有关。通过rna - chip和RT-PCR检测,FSHD和正常成肌细胞中检测到D4Z4很少或没有转录;来自一名FSHD患者、一名对照组和一名DNMT3B突变导致D4Z4低甲基化的患者(ICF综合征)的淋巴细胞;正常组织和癌组织。然而,rna - chip检测显示D4Z4在含有4号染色体的人-鼠体细胞杂交中转录。ChIP和RT-PCR显示在一些癌症和淋巴母细胞样细胞系中有卫星DNA转录,尽管水平很低。鉴于RNAi参与卫星DNA异染色化的证据,令人惊讶的是,最多只有一小部分卫星DNA与RNA Pol II相关。此外,我们的结果不支持先前假设的D4Z4序列在短的fshd链接阵列中与疾病相关的差异转录。
RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA
RNA interference (RNAi) is implicated in maintaining tandem DNA arrays as constitutive heterochromatin. We used chromatin immunoprecipitation with antibodies to RNA polymerase II (RNAPol-ChIP) to test for transcription of the following repeat arrays in human cells: subtelomeric D4Z4, pericentromeric satellite 2, and centromeric satellite α. D4Z4 has a promoter-like sequence upstream of an ORF in its 3.3-kb repeat unit. A short D4Z4 array at 4q35 is linked to facioscapulohumeral muscular dystrophy (FSHD). By RNAPol-ChIP and RT-PCR, little or no transcription of D4Z4 was detected in FSHD and normal myoblasts; lymphoblasts from an FSHD patient, a control, and a patient with D4Z4 hypomethylation due to mutation of DNMT3B (ICF syndrome); and normal or cancer tissues. However, RNAPol-ChIP assays indicated transcription of D4Z4 in a chromosome 4-containing human–mouse somatic cell hybrid. ChIP and RT-PCR showed satellite DNA transcription in some cancers and lymphoblastoid cell lines, although only at a low level. Given the evidence for the involvement of RNAi in satellite DNA heterochromatinization, it is surprising that, at most, a very small fraction of satellite DNA was associated with RNA Pol II. In addition, our results do not support the previously hypothesized disease-linked differential transcription of D4Z4 sequences in short, FSHD-linked arrays.