Singh Mala, Bag Sumit Kumar, Bhardwaj Archana, Ranjan Amol, Mantri Shrikant, Nigam Deepti, Sharma Yogesh Kumar, Sawant Samir Vishwanath
CSIR-National Botanical Research Institute, Rana Pratap Marg, Lucknow, 226001, India.
Academy of Scientific and Innovative Research (AcSIR), Anusandhan Bhawan, 2 Rafi Marg, New Delhi, 110 001, India.
BMC Plant Biol. 2015 Jan 21;15:13. doi: 10.1186/s12870-014-0404-2.
The nucleosome positioning regulates the gene expression and many other DNA-related processes in eukaryotes. Genome-wide mapping of nucleosome positions and correlation of genome-wide nucleosomal remodeling with the changes in the gene expression can help us understanding gene regulation on genome level.
In the present study, we correlate the gene expression and the genomic nucleosomal remodeling in response to salicylic acid (SA) treatment in A. thaliana. We have mapped genome-wide nucleosomes by performing tiling microarray using 146 bp mononucleosomal template DNA. The average nucleosomal coverage is approximately 346 bp per nucleosome both under the control and the SA-treated conditions. The nucleosomal coverage is more in the coding region than in the 5' regulatory regions. We observe approximately 50% nucleosomal remodeling on SA treatment where significant nucleosomal depletion and nucleosomal enrichment around the transcription start site (TSS) occur in SA induced genes and SA repressed genes respectively in response to SA treatment. Especially in the case of the SA-induced group, the nucleosomal remodeling over the minimal promoter in response to SA is especially significant in the Non-expresser of PR1 (NPR1)-dependent genes. A detailed investigation of npr1-1 mutant confirms a distinct role of NPR1 in the nucleosome remodeling over the core promoter. We have also identified several motifs for various hormonal responses; including ABRE elements in the remodeled nucleosomal regions around the promoter region in the SA regulated genes. We have further identified that the W-box and TGACG/C motif, reported to play an important role in SA-mediated induction, are enriched in nucleosome free regions (NFRs) of the promoter region of the SA induced genes.
This is the first study reporting genome-wide effects of SA treatment on the chromatin architecture of A. thaliana. It also reports significant role of NPR1 in genome-wide nucleosomal remodeling in response to SA.
核小体定位调节真核生物中的基因表达及许多其他与DNA相关的过程。全基因组范围内核小体位置的图谱绘制以及全基因组核小体重塑与基因表达变化的相关性,有助于我们从基因组水平理解基因调控。
在本研究中,我们将拟南芥中水杨酸(SA)处理后的基因表达与基因组核小体重塑进行了关联。我们使用146 bp的单核小体模板DNA通过平铺微阵列绘制了全基因组范围的核小体图谱。在对照和SA处理条件下,每个核小体的平均核小体覆盖范围约为346 bp。编码区的核小体覆盖范围比5'调控区更多。我们观察到SA处理后约50%的核小体重塑,其中SA诱导基因和SA抑制基因分别在转录起始位点(TSS)周围出现显著的核小体缺失和核小体富集,以响应SA处理。特别是在SA诱导组的情况下,响应SA时最小启动子上的核小体重塑在PR1非表达子(NPR1)依赖性基因中尤为显著。对npr1 - 1突变体的详细研究证实了NPR1在核心启动子上的核小体重塑中具有独特作用。我们还鉴定了几种不同激素反应的基序;包括SA调控基因启动子区域周围重塑的核小体区域中的ABRE元件。我们进一步鉴定出据报道在SA介导的诱导中起重要作用的W - box和TGACG/C基序,在SA诱导基因启动子区域的无核小体区域(NFRs)中富集。
这是第一项报道SA处理对拟南芥染色质结构全基因组影响的研究。它还报道了NPR1在响应SA的全基因组核小体重塑中的重要作用。