Rice nucleosome patterns undergo remodeling coincident with stress-induced gene expression

被引:14
作者
Zhang, Qi [1 ]
Oh, Dong-Ha [1 ]
DiTusa, Sandra Feuer [1 ]
RamanaRao, Mangu V. [2 ]
Baisakh, Niranjan [2 ]
Dassanayake, Maheshi [1 ]
Smith, Aaron P. [1 ]
机构
[1] Louisiana State Univ, Dept Biol Sci, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Ctr Agr, Sch Plant Environm & Soil Sci, Baton Rouge, LA 70803 USA
来源
BMC GENOMICS | 2018年 / 19卷
基金
美国国家科学基金会;
关键词
Nucleosome patterns; Phosphate starvation; Chromatin remodeling; Differential gene expression; MNase-seq; RNA-seq; Rice; PHOSPHATE STARVATION RESPONSES; YEAST PHO5 PROMOTER; DNA ELEMENTS; TATA BOX; IN-VIVO; GENOME; CHROMATIN; PHOSPHORUS; OCCUPANCY; DETERMINANTS;
D O I
10.1186/s12864-017-4397-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Formation of nucleosomes along eukaryotic DNA has an impact on transcription. Major transcriptional changes occur in response to low external phosphate (Pi) in plants, but the involvement of chromatin-level mechanisms in Pi starvation responses have not been investigated. Results: We mapped nucleosomes along with transcriptional changes after 24-h of Pi starvation in rice (Oryza sativa) by deep sequencing of micrococcal nuclease digested chromatin and ribosome-depleted RNA. We demonstrated that nucleosome patterns at rice genes were affected by both cis- and trans-determinants, including GC content and transcription. Also, categorizing rice genes by nucleosome patterns across the transcription start site (TSS) revealed nucleosome patterns that correlated with distinct functional categories of genes. We further demonstrated that Pi starvation resulted in numerous dynamic nucleosomes, which were enhanced at genes differentially expressed in response to Pi starvation. Conclusions: We demonstrate that rice nucleosome patterns are suggestive of gene functions, and reveal a link between chromatin remodeling and transcriptional changes in response to deficiency of a major macronutrient. Our findings help to enhance the understanding towards eukaryotic gene regulation at the chromatin level.
引用
收藏
页数:16
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