The Anaerobic Product Ethanol Promotes Autophagy-Dependent Submergence Tolerance in Arabidopsis.
The Anaerobic Product Ethanol Promotes Autophagy-Dependent Submergence Tolerance in Arabidopsis.
复制标题
厌氧产物乙醇促进拟南芥自噬依赖性淹没耐受性。
DOI:
10.3390/ijms21197361
复制
发表时间:
2020-10-05
影响因子:
5.6
通讯作者:
Xie LJ
中科院分区:
文献类型:
--
作者:
Yuan LB;Chen L;Zhai N;Zhou Y;Zhao SS;Shi LL;Xiao S;Yu LJ;Xie LJ
In response to hypoxia under submergence, plants switch from aerobic respiration to anaerobic fermentation, which leads to the accumulation of the end product, ethanol. We previously reported that Arabidopsis thaliana autophagy-deficient mutants show increased sensitivity to ethanol treatment, indicating that ethanol is likely involved in regulating the autophagy-mediated hypoxia response. Here, using a transcriptomic analysis, we identified 3909 genes in Arabidopsis seedlings that were differentially expressed in response to ethanol treatment, including 2487 upregulated and 1422 downregulated genes. Ethanol treatment significantly upregulated genes involved in autophagy and the detoxification of reactive oxygen species. Using transgenic lines expressing AUTOPHAGY-RELATED PROTEIN 8e fused to green fluorescent protein (GFP-ATG8e), we confirmed that exogenous ethanol treatment promotes autophagosome formation in vivo. Phenotypic analysis showed that deletions in the alcohol dehydrogenase gene in adh1 mutants result in attenuated submergence tolerance, decreased accumulation of ATG proteins, and diminished submergence-induced autophagosome formation. Compared to the submergence-tolerant Arabidopsis accession Columbia (Col-0), the submergence-intolerant accession Landsberg erecta (Ler) displayed hypersensitivity to ethanol treatment; we linked these phenotypes to differences in the functions of ADH1 and the autophagy machinery between these accessions. Thus, ethanol promotes autophagy-mediated submergence tolerance in Arabidopsis.
登录
查看更多内容
影响因子:
7.4
作者:
Bailey-Serres, Julia;Lee, Seung Cho;Brinton, Erin
通讯作者:
Brinton, Erin
影响因子:
13.3
作者:
Chen L;Liao B;Qi H;Xie LJ;Huang L;Tan WJ;Zhai N;Yuan LB;Zhou Y;Yu LJ;Chen QF;Shu W;Xiao S
通讯作者:
Xiao S
影响因子:
5.6
作者:
Banti V;Giuntoli B;Gonzali S;Loreti E;Magneschi L;Novi G;Paparelli E;Parlanti S;Pucciariello C;Santaniello A;Perata P
通讯作者:
Perata P
DOI:
10.1111/j.1530-0277.2012.01742.x
发表时间:
2012-08
期刊:
Alcoholism, clinical and experimental research
影响因子:
--
作者:
Dolganiuc A;Thomes PG;Ding WX;Lemasters JJ;Donohue TM Jr
通讯作者:
Donohue TM Jr
影响因子:
7.4
作者:
Giuntoli, Beatrice;Perata, Pierdomenico
通讯作者:
Perata, Pierdomenico