Phosphoproteome analysis reveals the involvement of protein dephosphorylation in ethylene-induced corolla senescence in petunia.
Phosphoproteome analysis reveals the involvement of protein dephosphorylation in ethylene-induced corolla senescence in petunia.
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磷酸蛋白质组分析揭示蛋白质去磷酸化参与乙烯诱导的矮牵牛花冠衰老
DOI:
10.1186/s12870-021-03286-x
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发表时间:
2021-11-03
影响因子:
5.3
通讯作者:
Liu J
中科院分区:
文献类型:
--
作者:
Zhong S;Sang L;Zhao Z;Deng Y;Liu H;Yu Y;Liu J
BackgroundSenescence represents the last stage of flower development. Phosphorylation is the key posttranslational modification that regulates protein functions, and kinases may be more required than phosphatases during plant growth and development. However, little is known about global phosphorylation changes during flower senescence.ResultsIn this work, we quantitatively investigated the petunia phosphoproteome following ethylene or air treatment. In total, 2170 phosphosites in 1184 protein groups were identified, among which 2059 sites in 1124 proteins were quantified. To our surprise, treatment with ethylene resulted in 697 downregulated and only 117 upregulated phosphosites using a 1.5-fold threshold (FDR < 0.05), which showed that ethylene negatively regulates global phosphorylation levels and that phosphorylation of many proteins was not necessary during flower senescence. Phosphoproteome analysis showed that ethylene regulates ethylene and ABA signalling transduction pathways via phosphorylation levels. One of the major targets of ethylene-induced dephosphorylation is the plant mRNA splicing machinery, and ethylene treatment increases the number of alternative splicing events of precursor RNAs in petunia corollas.ConclusionsProtein dephosphorylation could play an important role in ethylene-induced senescence, and ethylene treatment increased the number of AS precursor RNAs in petunia corollas.
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影响因子:
8.7
作者:
Du L;Song J;Forney C;Palmer LC;Fillmore S;Zhang Z
通讯作者:
Zhang Z
DOI:
10.1073/pnas.011405198
发表时间:
2001-01-02
影响因子:
11.1
作者:
Frye, CA;Tang, DZ;Innes, RW
通讯作者:
Innes, RW
影响因子:
--
作者:
Chen, Ruiqiang;Binder, Brad M.;Cooper, Bret
通讯作者:
Cooper, Bret
影响因子:
6.9
作者:
Bai S;Willard B;Chapin LJ;Kinter MT;Francis DM;Stead AD;Jones ML
通讯作者:
Jones ML
影响因子:
7.2
作者:
Joo, Sunjoo;Liu, Yidong;Zhang, Shuqun
通讯作者:
Zhang, Shuqun