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991.
Silvia F. Carambula 《Biochemical and biophysical research communications》2009,388(2):418-158
Apoptosis in the bovine embryo cannot be induced by activators of the extrinsic apoptosis pathway until the 8-16-cell stage. Depolarization of mitochondria with the decoupling agent carbonyl cyanide 3-chlorophenylhydrazone (CCCP) can activate caspase-3 in 2-cell embryos but DNA fragmentation does not occur. Here we hypothesized that the repression of apoptosis is caused by methylation of DNA and deacetylation of histones. To test this hypothesis, we evaluated whether reducing DNA methylation by 5-aza-2′-deoxycytidine (AZA) or inhibition of histone deacetylation by trichostatin-A (TSA) would make 2-cell embryos susceptible to DNA fragmentation caused by CCCP. The percent of blastomeres positive for TUNEL was affected by a treatment × CCCP interaction (P < 0.0001). CCCP did not cause a large increase in the percent of cells positive for TUNEL in embryos treated with vehicle but did increase the percent of cells that were TUNEL positive if embryos were pretreated with AZA or TSA. Immunostaining using an antibody against 5-methyl-cytosine antibody revealed that AZA and TSA reduced DNA methylation. In conclusion, disruption of DNA methylation and histone deacetylation removes the block to apoptosis in bovine 2-cell embryos. 相似文献
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PKD2 gene encodes a critical cation channel protein that plays important roles in various developmental processes and is usually
evolutionarily conserved. In the present study, we analyzed the evolutionary patterns of PKD2 and its homologous genes (PKD2L1, PKD2L2) from nine mammalian species. In this study, we demonstrated the orthologs of PKD2 gene family evolved under a dominant purifying selection force. Our results in combination with the reported evidences from
functional researches suggested the entire PKD2 gene family are conserved and perform essential biological roles during mammalian evolution. In rodents, PKD2 gene family members appeared to have evolved more rapidly than other mammalian lineages, probably resulting from relaxation
of purifying selection. However, positive selection imposed on synonymous sites also potentially contributed to this case.
For the paralogs, our results implied that PKD2L2 genes evolved under a weaker purifying selection constraint than PKD2 and PKD2L1 genes. Interestingly, some loop regions of transmembrane domain of PKD2L2 exhibited higher P
N/P
S ratios than expected, suggesting these regions are more functional divergent in organisms and worthy of special attention.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.
Chun Ye, Huan Sun have contributed equally to this work. 相似文献
994.
ROOT GORELICK JESSICA CARPINONE 《Biological journal of the Linnean Society. Linnean Society of London》2009,98(4):707-728
Sex is generally thought of as meiosis, conjugation, and syngamy, with the primary function of sex believed to be genetic mixing. However, conjugation does not occur with complete automixis, whereas syngamy does not occur with restitutional automixis. Self sex in the forms of automixis and autogamy does not include genetic mixing. Yet sex, including self sex, is necessary for most eukaryotic lineages. What is the purpose of sex without genetic mixing? Obligate self sex is not an evolutionary dead end, but holds the key to understanding the evolutionary origin, function, maintenance, and ubiquity of sex. We extend the rejuvenescence hypothesis that sex provides a necessary developmental reset for multicellular eukaryotes and even many unicellular eukaryotes. Sex reduces additive genetic variance of epigenetic signals, especially cytosine methylation, and of ploidy levels. Furthermore, we argue that syngamy is a modified form of meiosis that maintains ploidy and resets epigenetic signals. Epigenetic resetting is consistent with sex being induced by starvation or desiccation. Diminution of additive genetic variance is consistent with the origin and maintenance of an adaptive trait, sex, that has been present for approximately two billion years. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 98 , 707–728. 相似文献
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iTRAQ‐coupled 2‐D LC‐MS/MS analysis of protein profile associated with HBV‐modulated DNA methylation
The development of hepatocellular carcinoma (HCC) is believed to be associated with multiple risk factors, including the infection of hepatitis B virus (HBV). Based on the analysis of individual genes, evidence has indicated the association between HCC and HBV and has also been expanded to epigenetic regulation, with an involvement of HBV in the DNA methylation of the promoter of cellular target genes leading to changes in their expression. Proteomic study has been widely used to map a comprehensive protein profile, which in turn could provide a better understanding of underlying mechanisms of disease onset. In the present study, we performed a proteomic profiling by using iTRAQ‐coupled 2‐D LC/MS‐MS analysis to identify cellular genes down‐regulated in HBV‐producing HepG2.2.15 cells compared with HepG2 cells. A total of 15 proteins including S100A6 and Annexin A2 were identified by our approach. The significance of these cellular proteins as target of HBV‐mediated epigenetic regulation was supported by our validation assays, including their reactivation in cells treated with 5‐aza‐2′‐deoxycytidine (a DNA methyltransferase inhibitor) by real‐time RT‐PCR and Western blot analysis, as well as the DNA methylation status analysis by bisulfite genome sequencing. Our approach provides a comprehensive analysis of cellular target proteins to HBV‐mediated epigenetic regulation and further analysis should facilitate a better understanding of its involvement in HCC development. 相似文献
998.
Jian Huang 《中国科学:生命科学英文版》2009,52(1):31-42
Hepatocellular carcinoma is the main type of primary liver cancer, and also one of the most malignant tumors. At present,
the pathogenesis mechanisms of liver cancer are not entirely clear. It has been shown that inactivation of tumor suppressor
genes and activation of oncogenes play a significant role in carcinogenesis, caused by the genetic and epigenetic aberrance.
In the past, people generally thought that genetic mutation is a key event of tumor pathogenesis, and somatic mutation of
tumor suppressor genes is in particular closely associated with oncogenesis. With deeper understanding of tumors in recent
years, increasing evidence has shown that epigenetic silencing of those genes, as a result of aberrant hypermethylation of
CpG islands in promoters and histone modification, is essential to carcinogenesis and metastasis. The term epigenetics refers
to heritable changes in gene expression caused by regulation mechanisms, other than changes in the underlying DNA sequence.
Specific epigenetic processes include DNA methylation, genome imprinting, chromotin remodeling, histone modification and microRNA
regulations. This paper reviews recent epigenetics research progress in the hepatocellular carcinoma study, and tries to depict
the relationships between hepatocellular carcinomagenesis and DNA methylation as well as microRNA regulation.
Supported by National Basic Research Program of China (Grant No. 2006CD910402) and Science and Technology Commission of Shanghai
Municipality (Grant No. 05DZ22201 and 08JC1416400). 相似文献
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