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细胞核定位的更多硫积累蛋白1通过表观遗传调控拟南芥中的硫稳态。

Nuclear Localised MORE SULPHUR ACCUMULATION1 Epigenetically Regulates Sulphur Homeostasis in Arabidopsis thaliana.

作者信息

Huang Xin-Yuan, Chao Dai-Yin, Koprivova Anna, Danku John, Wirtz Markus, Müller Steffen, Sandoval Francisco J, Bauwe Hermann, Roje Sanja, Dilkes Brian, Hell Rüdiger, Kopriva Stanislav, Salt David E

机构信息

Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, United Kingdom.

Botanical Institute, Cluster of Excellence on Plant Sciences (CEPLAS), University of Cologne, Cologne, Germany.

出版信息

PLoS Genet. 2016 Sep 13;12(9):e1006298. doi: 10.1371/journal.pgen.1006298. eCollection 2016 Sep.

Abstract

Sulphur (S) is an essential element for all living organisms. The uptake, assimilation and metabolism of S in plants are well studied. However, the regulation of S homeostasis remains largely unknown. Here, we report on the identification and characterisation of the more sulphur accumulation1 (msa1-1) mutant. The MSA1 protein is localized to the nucleus and is required for both S-adenosylmethionine (SAM) production and DNA methylation. Loss of function of the nuclear localised MSA1 leads to a reduction in SAM in roots and a strong S-deficiency response even at ample S supply, causing an over-accumulation of sulphate, sulphite, cysteine and glutathione. Supplementation with SAM suppresses this high S phenotype. Furthermore, mutation of MSA1 affects genome-wide DNA methylation, including the methylation of S-deficiency responsive genes. Elevated S accumulation in msa1-1 requires the increased expression of the sulphate transporter genes SULTR1;1 and SULTR1;2 which are also differentially methylated in msa1-1. Our results suggest a novel function for MSA1 in the nucleus in regulating SAM biosynthesis and maintaining S homeostasis epigenetically via DNA methylation.

摘要

硫(S)是所有生物的必需元素。植物中硫的吸收、同化和代谢已得到充分研究。然而,硫稳态的调控在很大程度上仍不清楚。在此,我们报告了硫积累更多1(msa1-1)突变体的鉴定和特征。MSA1蛋白定位于细胞核,是生成S-腺苷甲硫氨酸(SAM)和DNA甲基化所必需的。细胞核定位的MSA1功能丧失导致根中SAM减少,即使在硫供应充足时也会引发强烈的缺硫反应,导致硫酸盐、亚硫酸盐、半胱氨酸和谷胱甘肽过度积累。补充SAM可抑制这种高硫表型。此外,MSA1突变会影响全基因组DNA甲基化,包括缺硫响应基因的甲基化。msa1-1中硫积累增加需要硫酸盐转运蛋白基因SULTR1;1和SULTR1;2表达增加,这两个基因在msa1-1中也存在差异甲基化。我们的结果表明,MSA1在细胞核中具有新功能,即通过DNA甲基化调控SAM生物合成并表观遗传地维持硫稳态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d7/5021336/d55474513012/pgen.1006298.g001.jpg

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