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  1. 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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  2. 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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