GC-Rich DNA Elements Enable Replication Origin Activity in the Methylotrophic Yeast Pichia pastoris

被引:33
作者
Liachko, Ivan [1 ]
Youngblood, Rachel A. [1 ]
Tsui, Kyle [2 ,3 ]
Bubb, Kerry L. [1 ]
Queitsch, Christine [1 ]
Raghuraman, M. K. [1 ]
Nislow, Corey [2 ,4 ]
Brewer, Bonita J. [1 ]
Dunham, Maitreya J. [1 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
[3] Univ Toronto, Dept Pharmaceut Sci, Toronto, ON, Canada
[4] Univ Toronto, Donnelly Ctr, Toronto, ON, Canada
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SCHIZOSACCHAROMYCES-POMBE GENOME; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTORS; NUCLEOSOME OCCUPANCY; FISSION YEAST; SEQUENCE; INITIATION; PROTEIN; SITES; CHROMATIN;
D O I
10.1371/journal.pgen.1004169
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The well-studied DNA replication origins of the model budding and fission yeasts are A/T-rich elements. However, unlike their yeast counterparts, both plant and metazoan origins are G/C-rich and are associated with transcription start sites. Here we show that an industrially important methylotrophic budding yeast, Pichia pastoris, simultaneously employs at least two types of replication origins-a G/C-rich type associated with transcription start sites and an A/T-rich type more reminiscent of typical budding and fission yeast origins. We used a suite of massively parallel sequencing tools to map and dissect P. pastoris origins comprehensively, to measure their replication dynamics, and to assay the global positioning of nucleosomes across the genome. Our results suggest that some functional overlap exists between promoter sequences and G/C-rich replication origins in P. pastoris and imply an evolutionary bifurcation of the modes of replication initiation.
引用
收藏
页数:13
相关论文
共 72 条
[1]   Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition [J].
Adey, Andrew ;
Morrison, Hilary G. ;
Asan ;
Xun, Xu ;
Kitzman, Jacob O. ;
Turner, Emily H. ;
Stackhouse, Bethany ;
MacKenzie, Alexandra P. ;
Caruccio, Nicholas C. ;
Zhang, Xiuqing ;
Shendure, Jay .
GENOME BIOLOGY, 2010, 11 (12)
[2]   Regulation of HSF1 Function in the Heat Stress Response: Implications in Aging and Disease [J].
Anckar, Julius ;
Sistonen, Lea .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80, 2011, 80 :1089-1115
[3]  
Bailey T L, 1994, Proc Int Conf Intell Syst Mol Biol, V2, P28
[4]   Combining evidence using p-values: application to sequence homology searches [J].
Bailey, TL ;
Gribskov, M .
BIOINFORMATICS, 1998, 14 (01) :48-54
[5]   Replication timing and its emergence from stochastic processes [J].
Bechhoefer, John ;
Rhind, Nicholas .
TRENDS IN GENETICS, 2012, 28 (08) :374-381
[6]   DNA replication in eukaryotic cells [J].
Bell, SP ;
Dutta, A .
ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 :333-374
[7]   Diversity of Eukaryotic DNA Replication Origins Revealed by Genome-Wide Analysis of Chromatin Structure [J].
Berbenetz, Nicolas M. ;
Nislow, Corey ;
Brown, Grant W. .
PLOS GENETICS, 2010, 6 (09)
[8]   Confidently Estimating the Number of DNA Replication Origins [J].
Bhaskar, Anand ;
Keich, Uri .
STATISTICAL APPLICATIONS IN GENETICS AND MOLECULAR BIOLOGY, 2010, 9 (01)
[9]   Prediction of Saccharomyces cerevisiae replication origins -: art. no. R22 [J].
Breier, AM ;
Chatterji, S ;
Cozzarelli, NR .
GENOME BIOLOGY, 2004, 5 (04)
[10]   THE LOCALIZATION OF REPLICATION ORIGINS ON ARS PLASMIDS IN SACCHAROMYCES-CEREVISIAE [J].
BREWER, BJ ;
FANGMAN, WL .
CELL, 1987, 51 (03) :463-471