The yeast genome is globally accessible in living cells

被引:1
作者
Prajapati, Hemant K. [1 ]
Eriksson, Peter R. [1 ]
Elizalde, Paul A. [1 ,2 ]
Coey, Christopher T. [1 ]
Xu, Zhuwei [1 ]
Clark, David J. [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Huma, NIH, Div Dev Biol, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, NIH JHU Grad Partnership Program, Baltimore, MD USA
关键词
SACCHAROMYCES-CEREVISIAE; GENE-EXPRESSION; NUCLEOSOMAL DNA; BUDDING YEAST; CHROMATIN; TRANSCRIPTION; CHD1; MECHANISMS; DYNAMICS; BINDING;
D O I
10.1038/s41594-024-01318-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eukaryotic genomes are packaged into chromatin, which is composed of condensed filaments of regularly spaced nucleosomes, resembling beads on a string. The nucleosome contains similar to 147 bp of DNA wrapped almost twice around a central core histone octamer. The packaging of DNA into chromatin represents a challenge to transcription factors and other proteins requiring access to their binding sites. Consequently, control of DNA accessibility is thought to play a key role in gene regulation. Here we measure DNA accessibility genome wide in living budding yeast cells by inducible expression of DNA methyltransferases. We find that the genome is globally accessible in living cells, unlike in isolated nuclei, where DNA accessibility is severely restricted. Gene bodies are methylated at only slightly slower rates than promoters, indicating that yeast chromatin is highly dynamic in vivo. In contrast, silenced loci and centromeres are strongly protected. Global shifts in nucleosome positions occur in cells as they are depleted of ATP-dependent chromatin remodelers, suggesting that nucleosome dynamics result from competition among these enzymes. We conclude that chromatin is in a state of continuous flux in living cells, but static in nuclei, suggesting that DNA packaging in yeast is not generally repressive.
引用
收藏
页码:247 / 256
页数:24
相关论文
共 75 条
[1]   Ten principles of heterochromatin formation and function [J].
Allshire, Robin C. ;
Madhani, Hiten D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2018, 19 (04) :229-244
[2]   Single molecule tracking of Ace1p in Saccharomyces cerevisiae defines a characteristic residence time for non-specific interactions of transcription factors with chromatin [J].
Ball, David A. ;
Mehta, Gunjan D. ;
Salomon-Kent, Ronit ;
Mazza, Davide ;
Morisaki, Tatsuya ;
Mueller, Florian ;
McNally, James G. ;
Karpova, Tatiana S. .
NUCLEIC ACIDS RESEARCH, 2016, 44 (21)
[3]   Mammalian ISWI and SWI/SNF selectively mediate binding of distinct transcription factors [J].
Barisic, Darko ;
Stadler, Michael B. ;
Iurlaro, Mario ;
Schuebeler, Dirk .
NATURE, 2019, 569 (7754) :136-+
[4]   Human SMARCA5 is continuously required to maintain nucleosome spacing [J].
Bomber, Monica L. ;
Wang, Jing ;
Liu, Qi ;
Barnett, Kelly R. ;
Layden, Hillary M. ;
Hodges, Emily ;
Stengel, Kristy R. ;
Hiebert, Scott W. .
MOLECULAR CELL, 2023, 83 (04) :507-+
[5]   Rapid accessibility of nucleosomal DNA in yeast on a second time scale [J].
Bucceri, Andrea ;
Kapitza, Kristin ;
Thoma, Fritz .
EMBO JOURNAL, 2006, 25 (13) :3123-3132
[6]   Cell-Cycle-Dependent Structural Transitions in the Human CENP-A Nucleosome In Vivo [J].
Bui, Minh ;
Dimitriadis, Emilios K. ;
Hoischen, Christian ;
An, Eunkyung ;
Quenet, Delphine ;
Giebe, Sindy ;
Nita-Lazar, Aleksandra ;
Diekmann, Stephan ;
Dalal, Yamini .
CELL, 2012, 150 (02) :317-326
[7]   The epigenetic basis of cellular heterogeneity [J].
Carter, Benjamin ;
Zhao, Keji .
NATURE REVIEWS GENETICS, 2021, 22 (04) :235-250
[8]   Accessibility of promoter DNA is not the primary determinant of chromatin-mediated gene regulation [J].
Chereji, Razvan V. ;
Eriksson, Peter R. ;
Ocampo, Josefina ;
Prajapati, Hemant K. ;
Clark, David J. .
GENOME RESEARCH, 2019, 29 (12) :1985-1995
[9]   Major Determinants of Nucleosome Positioning [J].
Chereji, Razvan V. ;
Clark, David J. .
BIOPHYSICAL JOURNAL, 2018, 114 (10) :2279-2289
[10]   MNase-Sensitive Complexes in Yeast: Nucleosomes and Non-histone Barriers [J].
Chereji, Razvan V. ;
Ocampo, Josefina ;
Clark, David J. .
MOLECULAR CELL, 2017, 65 (03) :565-+