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乙烯通过 SlMADS-RIN 转录因子对三个聚集的番茄 I 类小热休克伴侣蛋白基因的瞬时调控。

Transient regulation of three clustered tomato class-I small heat-shock chaperone genes by ethylene is mediated by SlMADS-RIN transcription factor.

机构信息

Sustainable Agricultural Systems Laboratory, USDA-ARS, Henry A. Wallace Beltsville Agricultural Research Center, Beltsville, MD, 20705-2350, USA.

Department of Biology, Penn State University at Harrisburg, Middletown, PA, 170-57, USA.

出版信息

Sci Rep. 2017 Jul 25;7(1):6474. doi: 10.1038/s41598-017-06622-0.

Abstract

Clustered class-I small heat-shock protein (sHSP) chaperone genes, SlHSP17.6, SlHSP20.0 and SlHSP20.1, in tomato are demonstrated to be transcriptionally regulated by ethylene during mature green (MG) fruit transition into ripening. These genes are constitutively expressed at MG fruit stage in two different tomato genotypes as well as in their ripening mutants, including rin, nor and Nr, and an ethylene-deficient transgenic line, ACS2-antisense. Notably, ethylene treatment of the MG fruit led to significant sHSP gene suppression in both wild-types, ACS2-antisense, nor/nor and Nr/Nr, but not the rin/rin mutant. Inability of ethylene to suppress sHSP genes in rin/rin mutant, which harbors MADS-RIN gene mutation, suggests that MADS-RIN transcription factor regulates the expression of these genes. Treatment of the wild type and ACS2-antisense fruit with the ethylene-signaling inhibitor, 1-methylcyclopropane (1-MCP), reversed the sHSP gene suppression. Transcripts of representative ethylene-responsive and ripening-modulated genes confirmed and validated sHSP transcript profile patterns. In silico analysis in conjunction with chromatin immunoprecipitation demonstrated MADS-RIN protein binding to specific CArG motifs present in the promoters of these chaperone genes. The results establish MADS-RIN protein as a transcriptional regulator of these chaperone genes in an ethylene-dependent manner, and that MADS-RIN protein-regulation of sHSPs is integral to tomato fruit ripening.

摘要

在番茄中,类-I 小热休克蛋白 (sHSP) 伴侣基因 SlHSP17.6、SlHSP20.0 和 SlHSP20.1 被证明在成熟绿 (MG) 果实向成熟转变过程中受乙烯的转录调控。这些基因在两个不同的番茄基因型及其成熟突变体 rin、nor 和 Nr 以及乙烯缺陷型转基因株系 ACS2-反义中在 MG 果实阶段持续表达。值得注意的是,乙烯处理 MG 果实导致野生型、ACS2-反义、nor/nor 和 Nr/Nr 中的 sHSP 基因显著下调,但 rin/rin 突变体除外。乙烯不能抑制 rin/rin 突变体(携带 MADS-RIN 基因突变)中的 sHSP 基因,表明 MADS-RIN 转录因子调节这些基因的表达。用乙烯信号抑制剂 1-甲基环丙烷 (1-MCP) 处理野生型和 ACS2-反义果实,逆转了 sHSP 基因的抑制。代表性的乙烯响应和成熟调节基因的转录本证实并验证了 sHSP 转录本谱模式。与染色质免疫沉淀相结合的计算机分析表明,MADS-RIN 蛋白与这些伴侣基因启动子中存在的特定 CArG 基序结合。结果确立了 MADS-RIN 蛋白作为这些伴侣基因在乙烯依赖性方式下的转录调节剂,并且 MADS-RIN 蛋白对 sHSPs 的调节是番茄果实成熟的重要组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffc/5527083/07e4f7d8625c/41598_2017_6622_Fig1_HTML.jpg

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