NAD+激酶
烟酰胺腺嘌呤二核苷酸
辅因子
生物
受体
信号转导
程序性细胞死亡
病菌
细胞生物学
化学
生物化学
细胞凋亡
酶
遗传学
作者
S. Horsefield,Hayden Burdett,Xiaoxiao Zhang,M.K. Manik,Yun Shi,Jian Chen,Tiancong Qi,Jonathan Gilley,Jhih‐Siang Lai,Maxwell X. Rank,Lachlan W. Casey,Weixi Gu,Daniel J. Ericsson,Gabriel Foley,Robert Hughes,Todd Bosanac,Mark von Itzstein,John P. Rathjen,Jeffrey D. Nanson,Mikael Bodén
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-08-23
卷期号:365 (6455): 793-799
被引量:484
标识
DOI:10.1126/science.aax1911
摘要
NAD depletion as pathogen response One way that plants respond to pathogen infection is by sacrificing the infected cells. The nucleotide-binding leucine-rich repeat immune receptors responsible for this hypersensitive response carry Toll/interleukin-1 receptor (TIR) domains. In two papers, Horsefield et al. and Wan et al. report that these TIR domains cleave the metabolic cofactor nicotinamide adenine dinucleotide (NAD + ) as part of their cell-death signaling in response to pathogens. Similar signaling links mammalian TIR-containing proteins to NAD + depletion during Wallerian degeneration of neurons. Science , this issue p. 793 , p. 799
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