Research article Topical Sections

Genome-wide maps of nucleosomes of the trichostatin A treated and untreated archiascomycetous yeast Saitoella complicata

  • Received: 28 January 2016 Accepted: 11 March 2016 Published: 15 March 2016
  • We investigated the effects of trichostatin A (TSA) on gene expression and nucleosome position in the archiascomycetous yeast Saitoella complicata. The expression levels of 154 genes increased in a TSA-concentration-dependent manner, while the levels of 131 genes decreased. Conserved genes between S. complicata and Schizosaccharomyces pombe were more commonly TSA-concentration-dependent downregulated genes than upregulated genes. We calculated the correlation coefficients of nucleosome position profiles within 300 nucleotides (nt) upstream of a translational start of S. complicata grown in the absence and the presence of TSA (3 μg/mL). We found that 20 (13.0%) of the 154 TSA-concentration-dependent upregulated genes and 22 (16.8%) of the 131 downregulated genes had different profiles (r < 0.4) between TSA-free and TSA-treated. Additionally, 59 (38.3%) of the 154 upregulated genes and 58 (44.3%) of the 131 downregulated genes had similar profiles (r > 0.8). We did not observe a GC content bias between the 300 nt upstream of the translational start of the TSA-concentration-dependent genes with conserved nucleosome positioning and the genes with different nucleosome positioning, suggesting that TSA-induced nucleosome position change is likely not related to DNA sequence. Most gene promoters maintained their nucleosome positioning even after TSA treatment, which may be related to DNA sequence. Enriched and depleted dinucleotides distribution of S. complicata around the midpoints of highly positioned nucleosome dyads was not similar to that of the phylogenetically close yeast Schizosaccharomyces pombe but similar to the basidiomycete Mixia osmundae, which has similar genomic GC content to that of S. complicata.

    Citation: Kenta Yamauchi, Shinji Kondo, Makiko Hamamoto, Yutaka Suzuki, Hiromi Nishida. Genome-wide maps of nucleosomes of the trichostatin A treated and untreated archiascomycetous yeast Saitoella complicata[J]. AIMS Microbiology, 2016, 2(1): 69-91. doi: 10.3934/microbiol.2016.1.69

    Related Papers:

  • We investigated the effects of trichostatin A (TSA) on gene expression and nucleosome position in the archiascomycetous yeast Saitoella complicata. The expression levels of 154 genes increased in a TSA-concentration-dependent manner, while the levels of 131 genes decreased. Conserved genes between S. complicata and Schizosaccharomyces pombe were more commonly TSA-concentration-dependent downregulated genes than upregulated genes. We calculated the correlation coefficients of nucleosome position profiles within 300 nucleotides (nt) upstream of a translational start of S. complicata grown in the absence and the presence of TSA (3 μg/mL). We found that 20 (13.0%) of the 154 TSA-concentration-dependent upregulated genes and 22 (16.8%) of the 131 downregulated genes had different profiles (r < 0.4) between TSA-free and TSA-treated. Additionally, 59 (38.3%) of the 154 upregulated genes and 58 (44.3%) of the 131 downregulated genes had similar profiles (r > 0.8). We did not observe a GC content bias between the 300 nt upstream of the translational start of the TSA-concentration-dependent genes with conserved nucleosome positioning and the genes with different nucleosome positioning, suggesting that TSA-induced nucleosome position change is likely not related to DNA sequence. Most gene promoters maintained their nucleosome positioning even after TSA treatment, which may be related to DNA sequence. Enriched and depleted dinucleotides distribution of S. complicata around the midpoints of highly positioned nucleosome dyads was not similar to that of the phylogenetically close yeast Schizosaccharomyces pombe but similar to the basidiomycete Mixia osmundae, which has similar genomic GC content to that of S. complicata.


    加载中
    [1] Igo-Kemenes T, Hörz W, Zachau HG (1982) Chromatin. Ann Rev Biochem 51: 89–121. doi: 10.1146/annurev.bi.51.070182.000513
    [2] Luger K, Mäder AW, Richmond RK, et al. (1997) Crystal structure of the nucleosome core particle at 2.8 Å resolution. Nature 389: 251–260.
    [3] Millar CB, Grunstein M (2006) Genome-wide patterns of histone modifications in yeast. Nat Rev Mol Cell Biol 7: 657–666. doi: 10.1038/nrm1986
    [4] Li B, Carey M, Workman JL (2007) The role of chromatin during transcription. Cell 128: 707–719. doi: 10.1016/j.cell.2007.01.015
    [5] Luger K, Richmond TJ (1998) The histone tails of the nucleosome. Curr Opin Genet Dev 8: 140–146. doi: 10.1016/S0959-437X(98)80134-2
    [6] Sasaki K, Ito T, Nishino N, et al. (2009) Real-time imaging of histone H4 hyperacetylation in living cells. Proc Natl Acad Sci USA 106: 16257–16262. doi: 10.1073/pnas.0902150106
    [7] Yoshida M, Horinouchi S, Beppu T (1995) Trichostatin A and trapoxin: novel chemical probes for the role of histone acetylation in chromatin structure and function. BioEssays 17: 423–430. doi: 10.1002/bies.950170510
    [8] Nishida H, Motoyama T, Suzuki Y, et al. (2010) Genome-wide maps of mononucleosomes and dinucleosomes containing hyperacetylated histones of Aspergillus fumigatus. PLOS ONE 5: e9916. doi: 10.1371/journal.pone.0009916
    [9] Liu Y, Leigh JW, Brinkmann H, et al. (2009) Phylogenomic analyses support the monophyly of Taphrinomycotina, including Schizosaccharomyces fission yeasts. Mol Biol Evol 26: 27–34.
    [10] Nishida H, Sugiyama J (1994) Archiascomycetes: detection of a major new lineage within the Ascomycota. Mycoscience 35: 361–366. doi: 10.1007/BF02268506
    [11] Goto S, Sugiyama J, Hamamoto M, et al. (1987) Saitoella, a new anamorph genus in the Cryptococcaceae to accommodate two Himalayan yeast isolates formerly identified as Rhodotorula glutinis. J Gen Appl Microbiol 33: 75–85. doi: 10.2323/jgam.33.75
    [12] Nishida H, Hamamoto M, Sugiyama J (2011) Draft genome sequencing of the enigmatic yeast Saitoella complicata. J Gen Appl Microbiol 57: 243–246. doi: 10.2323/jgam.57.243
    [13] Nishida H, Matsumoto T, Kondo S, et al. (2014) The early diverging ascomycetous budding yeast Saitoella complicata has three histone deacetylases belonging to the Clr6, Hos2, and Rpd3 lineages. J Gen Appl Microbiol 60: 7–12. doi: 10.2323/jgam.60.7
    [14] Ekwall K, Olsson T, Tumer BM, et al. (1997) Transient inhibitor of histone deacetylation alters the structural and functional imprint at fission yeast centromeres. Cell 91: 1021–1032. doi: 10.1016/S0092-8674(00)80492-4
    [15] Yamauchi K, Kondo S, Hamamoto M, et al. (2015) Draft genome sequence of the archiascomycetous yeast Saitoella complicata. Genome Announc 3: e00220–15.
    [16] Trapnell C, Pachter L, Salzberg SL (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25: 1105–1111. doi: 10.1093/bioinformatics/btp120
    [17] Li H, Handsaker B, Wysoker A, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25: 2078–2079. doi: 10.1093/bioinformatics/btp352
    [18] Ogasawara O, Mashima J, Kodama Y, et al. (2013) DDBJ new system and service refactoring. Nucleic Acids Res 41: D25–D29. doi: 10.1093/nar/gks1152
    [19] Robinson MD, McCarthy DJ, Smyth GK (2010) edgeR: a Bioconductor package for different expression analysis of digital gene expression data. Bioinformatics 26: 139–140. doi: 10.1093/bioinformatics/btp616
    [20] Valouev A, Johnson SM, Boyd SD, et al. (2011) Determinants of nucleosome organization in primary human cells. Nature 474: 516–520. doi: 10.1038/nature10002
    [21] Kaplan N, Moore IK, Fondufe-Mittendorf Y, et al. (2008) The DNA-encoded nucleosome organization of a eukaryotic genome. Nature 458: 362–366.
    [22] Altschul SF, Gish W, Miller W, et al. (1990) Basic local alignment search tool. J Mol Biol 215: 403–410. doi: 10.1016/S0022-2836(05)80360-2
    [23] Amit M, Donyo M, Hollander D, et al. (2012) Differential GC content between exons and introns establishes distinct strategies of splice-site recognition. Cell Rep 1: 543–556. doi: 10.1016/j.celrep.2012.03.013
    [24] Nishida H, Katayama T, Suzuki Y, et al. (2013) Base composition and nucleosome density in exonic and intronic regions in genes of the filamentous ascomycetes Aspergillus nidulans and Aspergillus oryzae. Gene 525: 5–10. doi: 10.1016/j.gene.2013.04.077
    [25] Yu J, Hu S, Wang J, et al. (2002) A draft sequence of the rice genome (Oryza sativa L. ssp. indica). Science 296: 79–92.
    [26] Nishida H, Kondo S, Matsumoto T, et al. (2012) Characteristics of nucleosomes and linker DNA regions on the genome of the basidiomycete Mixia osmundae revealed by mono- and dinucleosome mapping. Open Biol 2: 120043. doi: 10.1098/rsob.120043
    [27] Graessle S, Dangl M, Haas H, et al. (2000) Characterization of two putative histone deacetylase genes from Aspergillus nidulans. Biochim Biophys Acta 1492: 120–126. doi: 10.1016/S0167-4781(00)00093-2
    [28] Andersson R, Enroth S, Rada-Iglesias A, et al. (2009) Nucleosomes are well positioned in exons and carry characteristic histone modifications. Genome Res 19: 1732–1741. doi: 10.1101/gr.092353.109
    [29] Chen W, Luo L, Zhang L (2010) The organization of nucleosomes around splice sites. Nucleic Acids Res 38: 2788–2798. doi: 10.1093/nar/gkq007
    [30] Schwartz S, Ast G (2010) Chromatin density and splicing density: on the cross-talk between chromatin structure and splicing. EMBO J 29: 1629–1636. doi: 10.1038/emboj.2010.71
    [31] Schwartz S, Meshorer E, Ast G (2009) Chromatin organization marks exon–intron structure. Nat Struct Mol Biol 16: 990–995. doi: 10.1038/nsmb.1659
    [32] Tilgner H, Nikolaou C, Althammer S, et al. (2009) Nucleosome positioning as a determinant of exon recognition. Nat Struct Mol Biol 16: 996–1001. doi: 10.1038/nsmb.1658
    [33] Tsankov A, Yanagisawa Y, Rhind N, et al. (2011) Evolutionary divergence of intrinsic and trans-regulated nucleosome positioning sequences reveals plastic rules for chromatin organization. Genome Res 21: 1851–1862. doi: 10.1101/gr.122267.111
    [34] Shim YS, Choi Y, Kang K, et al. (2012) Hrp3 controls nucleosome positioning to suppress non-coding transcription in eu- and heterochromatin. EMBO J 31: 4375–4387. doi: 10.1038/emboj.2012.267
  • Reader Comments
  • © 2016 the Author(s), licensee AIMS Press. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Metrics

Article views(5641) PDF downloads(1387) Cited by(2)

Article outline

Figures and Tables

Figures(7)  /  Tables(2)

/

DownLoad:  Full-Size Img  PowerPoint
Return
Return

Catalog