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  1. Article: Allele-specific germ cell epimutation in the spacer promoter of the 45S ribosomal RNA gene after Cr(III) exposure.

    Shiao, Yih-Horng / Crawford, Erik B / Anderson, Lucy M / Patel, Pritesh / Ko, Kinarm

    Toxicology and applied pharmacology

    2005  Volume 205, Issue 3, Page(s) 290–296

    Abstract: Paternal exposure of mice to Cr(III) causes increased tumor risk in offspring; an epigenetic mechanism has been hypothesized. Representational difference analysis of gene methylation in sperm revealed hypomethylation in the 45S ribosomal RNA (rRNA) gene ... ...

    Abstract Paternal exposure of mice to Cr(III) causes increased tumor risk in offspring; an epigenetic mechanism has been hypothesized. Representational difference analysis of gene methylation in sperm revealed hypomethylation in the 45S ribosomal RNA (rRNA) gene after Cr(III) exposure, compared with controls. The most striking effects were seen in the rRNA spacer promoter, a region in the intergenic region of rRNA gene clusters that can influence transcription. Methylation of the rRNA spacer promoter has not been studied heretofore. Sperm DNAs from Cr(III)-treated and control mice were modified by the bisulfite method followed by PCR amplification of the spacer promoter, including 27 CpG sites. Cloning and dideoxy sequencing identified sequence variants (T or G at base -2214) in the spacer promoter. The T allele had less DNA methylation than the G allele in control mice (17 of 17 clones vs. 42 of 72 clones, P = 0.0004). In spite of diversity of sperm DNA methylation patterns, the DNA clones from Cr(III)-exposed mice had fewer methylated CpG sites, by an average of 19% (P < 0.0001). This difference was limited to the G allele. The pyrosequencing technique was applied to quantify the percentage of methylation directly from amplified PCR products. Strikingly, for nine CpG sites including the spacer promoter core region, hypomethylation was highly significant in the Cr(III)-treated group (paired T test, P < 0.0001). Thus, one allele of the 45S rRNA spacer promoter is hypomethylated in sperm germ cells after Cr(III) exposure. This epimutation may lead to increase of tumor risk in the offspring.
    MeSH term(s) Alleles ; Animals ; Chromium/adverse effects ; Chromium/chemistry ; Clone Cells/drug effects ; CpG Islands/drug effects ; CpG Islands/genetics ; DNA/chemistry ; DNA/isolation & purification ; DNA Methylation/drug effects ; Germ Cells/physiology ; Male ; Methylation ; Mice ; Mutation/drug effects ; Mutation/genetics ; Polymorphism, Genetic ; Promoter Regions, Genetic/genetics ; RNA, Ribosomal/drug effects ; RNA, Ribosomal/genetics ; RNA, Ribosomal/metabolism ; Sequence Analysis, DNA/methods ; Species Specificity ; Spermatozoa/chemistry ; Spermatozoa/drug effects
    Chemical Substances RNA, Ribosomal ; RNA, ribosomal, 45S ; Chromium (0R0008Q3JB) ; DNA (9007-49-2)
    Language English
    Publishing date 2005-06-15
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 204477-8
    ISSN 1096-0333 ; 0041-008X
    ISSN (online) 1096-0333
    ISSN 0041-008X
    DOI 10.1016/j.taap.2004.10.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Molecular and organismal changes in offspring of male mice treated with chemical stressors.

    Shiao, Yih-Horng / Leighty, Robert M / Wang, Cuiju / Ge, Xin / Crawford, Erik B / Spurrier, Joshua M / McCann, Sean D / Fields, Janet R / Fornwald, Laura / Riffle, Lisa / Driver, Craig / Kasprzak, Kazimierz S / Quiñones, Octavio A / Wilson, Ralph E / Travlos, Gregory S / Alvord, W Gregory / Anderson, Lucy M

    Environmental and molecular mutagenesis

    2012  Volume 53, Issue 5, Page(s) 392–407

    Abstract: Both gene methylation changes and genetic instability have been noted in offspring of male rodents exposed to radiation or chemicals, but few specific gene targets have been established. Previously, we identified the gene for ribosomal RNA, rDNA, as ... ...

    Abstract Both gene methylation changes and genetic instability have been noted in offspring of male rodents exposed to radiation or chemicals, but few specific gene targets have been established. Previously, we identified the gene for ribosomal RNA, rDNA, as showing methylation change in sperm of mice treated with the preconceptional carcinogen, chromium(III) chloride. rDNA is a critical cell growth regulator. Here, we investigated the effects of paternal treatments on rDNA in offspring tissue. A total of 93 litters and 758 offspring were obtained, permitting rigorous mixed-effects models statistical analysis of the results. We show that the offspring of male mice treated with Cr(III) presented increased methylation in a promoter sequence of the rDNA gene, specifically in lung. Furthermore polymorphic variants of the multi-copy rDNA genes displayed altered frequencies indicative of structural changes, as a function of both tissue type and paternal treatments. Organismal effects also occurred: some groups of offspring of male mice treated with either Cr(III) or its vehicle, acidic saline, compared with those of untreated mice, had altered average body and liver weights and levels of serum glucose and leptin. Males treated directly with Cr(III) or acidic saline presented serum hormone changes consistent with a stress response. These results establish for the first time epigenetic and genetic instability effects in a gene of central physiological importance, in offspring of male mice exposed preconceptionally to chemicals, possibly related to a stress response in these males.
    MeSH term(s) Animals ; DNA Methylation ; DNA, Ribosomal/genetics ; Genotype ; Insulin-Like Growth Factor I/genetics ; Male ; Mice ; Regulatory Sequences, Nucleic Acid ; Stress, Physiological/drug effects
    Chemical Substances DNA, Ribosomal ; Insulin-Like Growth Factor I (67763-96-6)
    Language English
    Publishing date 2012-06
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural
    ZDB-ID 639145-x
    ISSN 1098-2280 ; 0893-6692
    ISSN (online) 1098-2280
    ISSN 0893-6692
    DOI 10.1002/em.21701
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Ontogeny-driven rDNA rearrangement, methylation, and transcription, and paternal influence.

    Shiao, Yih-Horng / Leighty, Robert M / Wang, Cuiju / Ge, Xin / Crawford, Erik B / Spurrier, Joshua M / McCann, Sean D / Fields, Janet R / Fornwald, Laura / Riffle, Lisa / Driver, Craig / Quiñones, Octavio A / Wilson, Ralph E / Kasprzak, Kazimierz S / Travlos, Gregory S / Alvord, W Gregory / Anderson, Lucy M

    PloS one

    2011  Volume 6, Issue 7, Page(s) e22266

    Abstract: Gene rearrangement occurs during development in some cell types and this genome dynamics is modulated by intrinsic and extrinsic factors, including growth stimulants and nutrients. This raises a possibility that such structural change in the genome and ... ...

    Abstract Gene rearrangement occurs during development in some cell types and this genome dynamics is modulated by intrinsic and extrinsic factors, including growth stimulants and nutrients. This raises a possibility that such structural change in the genome and its subsequent epigenetic modifications may also take place during mammalian ontogeny, a process undergoing finely orchestrated cell division and differentiation. We tested this hypothesis by comparing single nucleotide polymorphism-defined haplotype frequencies and DNA methylation of the rDNA multicopy gene between two mouse ontogenic stages and among three adult tissues of individual mice. Possible influences to the genetic and epigenetic dynamics by paternal exposures were also examined for Cr(III) and acid saline extrinsic factors. Variables derived from litters, individuals, and duplicate assays in large mouse populations were examined using linear mixed-effects model. We report here that active rDNA rearrangement, represented by changes of haplotype frequencies, arises during ontogenic progression from day 8 embryos to 6-week adult mice as well as in different tissue lineages and is modifiable by paternal exposures. The rDNA methylation levels were also altered in concordance with this ontogenic progression and were associated with rDNA haplotypes. Sperm showed highest level of methylation, followed by lungs and livers, and preferentially selected haplotypes that are positively associated with methylation. Livers, maintaining lower levels of rDNA methylation compared with lungs, expressed more rRNA transcript. In vitro transcription demonstrated haplotype-dependent rRNA expression. Thus, the genome is also dynamic during mammalian ontogeny and its rearrangement may trigger epigenetic changes and subsequent transcriptional controls, that are further influenced by paternal exposures.
    MeSH term(s) Animals ; Base Sequence ; CpG Islands/genetics ; DNA Methylation/genetics ; DNA, Ribosomal/genetics ; Epigenesis, Genetic ; Gene Rearrangement/genetics ; Haplotypes/genetics ; Male ; Mice ; Models, Genetic ; Molecular Sequence Data ; Paternal Exposure ; Promoter Regions, Genetic/genetics ; Sequence Analysis, DNA ; Transcription, Genetic
    Chemical Substances DNA, Ribosomal
    Language English
    Publishing date 2011-07-12
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0022266
    Database MEDical Literature Analysis and Retrieval System OnLINE

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