期刊文献+

Decoding the Epigenetic Language of Plant Development 被引量:11

Decoding the Epigenetic Language of Plant Development
原文传递
导出
摘要 Epigenetics refers to the study of heritable changes in gene expression or cellular phenotype without changes in DNA sequence. Epigenetic regulation of gene expression is accomplished by DNA methylation, histone modifications, histone variants, chromatin remodeling, and may involve small RNAs. DNA methylation at cytosine is carried out by enzymes called DNA Methyltransferases and is involved in many cellular processes, such as silencing of transposable elements and pericentromeric repeats, X-chromosome inactivation and genomic imprinting, etc. Histone modifications refer to posttranslational covalent attachment of chemical groups onto histones such as phosphorylation, acetylation, and methylation, etc. Histone variants, the non-canonical histones with amino acid sequences divergent from canonical histones, can have different epigenetic impacts on the genome from canonical histones. Higher-order chromatin structures maintained or modified by chromatin remodeling proteins also play important roles in regulating gene expression. Small non-coding RNAs play various roles in the regulation of gene expression at preas well as posttranscriptional levels. A special issue of Molecular Plant on 'Epigenetics and Plant Development' (Volume 4, Number 2, 2009) published a variety of articles covering many aspects of epigenetic regulation of plant development. We have tried here to present a bird's-eye view of these credible efforts towards understanding the mysterious world of epigenetics. The majority of the articles are about the chromatin modifying proteins, including histone modifiers, histone variants, and chromatin remodeling pro- teins that regulate various developmental processes, such as flowering time, vernalization, stem cell maintenance, and response to hormonal and environmental stresses, etc. Regulation of expression of seed transcriptome, involvement of direct tandem repeat elements in the PHE1 imprinting in addition to PcG proteins activity, paramutation, and epigenetic barriers in species hybridization are described well. The last two papers are about the Pol V-mediated heterochromatin formation in- dependent of the 24nt-siRNA and the effect of genome position and tissue type on epigenetic regulation of gene expression. These findings not only further our current understanding of epigenetic mechanisms involved in many biological phenomena, but also pave the path for the future work, by raising many new questions that are discussed in the following lines. Epigenetics refers to the study of heritable changes in gene expression or cellular phenotype without changes in DNA sequence. Epigenetic regulation of gene expression is accomplished by DNA methylation, histone modifications, histone variants, chromatin remodeling, and may involve small RNAs. DNA methylation at cytosine is carried out by enzymes called DNA Methyltransferases and is involved in many cellular processes, such as silencing of transposable elements and pericentromeric repeats, X-chromosome inactivation and genomic imprinting, etc. Histone modifications refer to posttranslational covalent attachment of chemical groups onto histones such as phosphorylation, acetylation, and methylation, etc. Histone variants, the non-canonical histones with amino acid sequences divergent from canonical histones, can have different epigenetic impacts on the genome from canonical histones. Higher-order chromatin structures maintained or modified by chromatin remodeling proteins also play important roles in regulating gene expression. Small non-coding RNAs play various roles in the regulation of gene expression at preas well as posttranscriptional levels. A special issue of Molecular Plant on 'Epigenetics and Plant Development' (Volume 4, Number 2, 2009) published a variety of articles covering many aspects of epigenetic regulation of plant development. We have tried here to present a bird's-eye view of these credible efforts towards understanding the mysterious world of epigenetics. The majority of the articles are about the chromatin modifying proteins, including histone modifiers, histone variants, and chromatin remodeling pro- teins that regulate various developmental processes, such as flowering time, vernalization, stem cell maintenance, and response to hormonal and environmental stresses, etc. Regulation of expression of seed transcriptome, involvement of direct tandem repeat elements in the PHE1 imprinting in addition to PcG proteins activity, paramutation, and epigenetic barriers in species hybridization are described well. The last two papers are about the Pol V-mediated heterochromatin formation in- dependent of the 24nt-siRNA and the effect of genome position and tissue type on epigenetic regulation of gene expression. These findings not only further our current understanding of epigenetic mechanisms involved in many biological phenomena, but also pave the path for the future work, by raising many new questions that are discussed in the following lines.
出处 《Molecular Plant》 SCIE CAS CSCD 2010年第4期719-728,共10页 分子植物(英文版)
关键词 Chromatin structure and remodeling EPIGENETICS gene silencing flowering. Chromatin structure and remodeling epigenetics gene silencing flowering.
  • 相关文献

参考文献15

二级参考文献964

  • 1Paulus M Fong,Lu Tian,Z Jeffrey Chen.Arabidopsis thaliana histone deacetylase1(AtHD1)is localized in euchromatic regions and demonstrates histone deacetylase activity in vitro[J].Cell Research,2006,16(5):479-488. 被引量:6
  • 2Kao, C.Y., Cocciolone, S.M., Vasil, I.K., and McCarty, D.R. (1996). Localization and interaction of the cis-acting elements for abscisic acid, VIVIPAROUSI, and light activation of the C1 gene of maize. Plant Cell. 8, 1171-1179.
  • 3Kehle, J., Beuchle, D., Treuheit, S., Christen, B., Kennison, J.A., Bienz, M., and Miiller, J. (1998). dMi-2, a hunchback-interacting protein that functions in Polycomb repression. Science. 282, 1897-1900.
  • 4Keith, K., Kraml, M., Dengler, N.G., and McCourt, R (1994). fusca3: a heterochronic mutation affecting late embryo development in Arabidopsis. Plant Cell. 6, 589-600.
  • 5Kohler, C., and Villar, C.B. (2008). Programming of gene expression by Polycomb group proteins. Trends Cell Biol. 18, 236-243.
  • 6Kohler, C., Hennig, L., Spillane, C., Pien, S., Gruissem, W., and Grossniklaus. U. (2003). The Polycomb-group protein MEDEA regulates seed development by controlling expression of the MADS-box gene PHERES1. Genes Dev. 17, 1540-1553.
  • 7Konev, A.Y, et al. (2007). CHD1 motor protein is required for deposition of histone variant H3.3 into chromatin in vivo. Science. 317, 1087-1090.
  • 8Koornneef, M., Reuling, G., and Karssen, C.M. (1984). The isolation and characterization of abscisic acid-insensitive mutants of Arabidopsis thaliana. Physiologia Plantarum. 61,377-383.
  • 9Kouzarides, T. (2007). Chromatin modifications and their function. Cell. 128, 693-705.
  • 10Kwon, C., Hibara, K., Pfluger, J., Bezhani, S., Metha, H., Aida, M., Tasaka, M., and Wagner, D. (2006). A role for chromatin remodeling in regulation of CUC gene expression in the Arabidopsis cotyledon boundary. Development. 133, 3223-3230.

共引文献132

同被引文献73

引证文献11

二级引证文献54

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部