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SUB1A-1锚定了一个用于水稻耐淹性表观遗传和转录调控的调控级联。

SUB1A-1 anchors a regulatory cascade for epigenetic and transcriptional controls of submergence tolerance in rice.

作者信息

Lin Chih-Cheng, Lee Wan-Jia, Zeng Cyong-Yu, Chou Mei-Yi, Lin Ting-Jhen, Lin Choun-Sea, Ho Meng-Chiao, Shih Ming-Che

机构信息

Agricultural Biotechnology Research Center, Academia Sinica, Taipei 11529, Taiwan.

Institute of Plant Biology, National Taiwan University, Taipei 10617, Taiwan.

出版信息

PNAS Nexus. 2023 Jul 11;2(7):pgad229. doi: 10.1093/pnasnexus/pgad229. eCollection 2023 Jul.

Abstract

Most rice () cultivars cannot survive under prolonged submergence. However, some ssp. cultivars, such as FR13A, are highly tolerant owing to the () allele, which encodes a Group VII ethylene-responsive factor (ERFVII) protein; other submergence-intolerant cultivars contain a allele. The two alleles differ only by a single substitution at the 186 amino acid position from serine in SUB1A-1 to proline in SUB1A-2 resulting in only SUB1A-1 being able to be phosphorylated. Two other ERFVIIs, and , function downstream of SUB1A-1 to form a regulatory cascade in response to submergence stress. Here, we show that SUB1A-1, but not SUB1A-2, interacts with ADA2b of the ADA2b-GCN5 acetyltransferase complex, in which GCN5 functions as a histone acetyltransferase. Phosphorylation of SUB1A-1 at serine 186 enhances the interaction of SUB1A-1 with ADA2b. and expression was induced under submergence, suggesting that these two genes might play roles in response to submergence stress. In transient assays, binding of SUB1A-1 to the promoter and transcription were highly induced when SUB1A-1 was expressed together with the ADA2b-GCN5 acetyltransferase complex. Taken together, these results suggest that phospho-SUB1A-1 recruits the ADA2-GCN5 acetyltransferase complex to modify the chromatin structure of the promoter regions and activate gene expression, which in turn enhances rice submergence tolerance.

摘要

大多数水稻()品种在长时间淹水条件下无法存活。然而,一些稻种(ssp.)品种,如FR13A,由于SUB1()等位基因而具有高度耐受性,该等位基因编码一种VII类乙烯响应因子(ERFVII)蛋白;其他不耐淹的品种则含有sub1()等位基因。这两个等位基因仅在第186个氨基酸位置有一个单碱基替换,从SUB1A - 1中的丝氨酸变为SUB1A - 2中的脯氨酸,导致只有SUB1A - 1能够被磷酸化。另外两个ERFVII蛋白,SNORKEL1和SNORKEL2,在SUB1A - 1的下游起作用,以形成应对淹水胁迫的调控级联反应。在这里,我们表明SUB1A - 1而非SUB1A - 2与ADA2b - GCN5乙酰转移酶复合物中的ADA2b相互作用,其中GCN5作为组蛋白乙酰转移酶发挥作用。SUB1A - 1在丝氨酸186处的磷酸化增强了SUB1A - 1与ADA2b的相互作用。SNORKEL1和SNORKEL2的表达在淹水条件下被诱导,表明这两个基因可能在应对淹水胁迫中发挥作用。在瞬时分析中,当SUB1A - 1与ADA2b - GCN5乙酰转移酶复合物一起表达时,SUB1A - 1与SNORKEL1启动子的结合以及SNORKEL1转录被高度诱导。综上所述,这些结果表明磷酸化的SUB1A - 1募集ADA2 - GCN5乙酰转移酶复合物来修饰SNORKEL1启动子区域的染色质结构并激活基因表达,进而增强水稻的淹水耐受性。

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