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RNA-Seq 分析鉴定“红早酥”梨皮花青苷生物合成相关的转录因子及. 的功能研究

RNA-Seq Analysis Identifies Transcription Factors Involved in Anthocyanin Biosynthesis of 'Red Zaosu' Pear Peel and Functional Study of .

机构信息

College of Life Science, Hebei Normal University, Shijiazhuang 050024, China.

Institute of Biotechnology and Food Science, Hebei Academy of Agriculture and Forestry Sciences, Shijiazhuang 050051, China.

出版信息

Int J Mol Sci. 2022 Apr 27;23(9):4798. doi: 10.3390/ijms23094798.

Abstract

Red-skinned pears are favored by people for their attractive appearance and abundance of anthocyanins. However, the molecular basis of anthocyanin biosynthesis in red pears remains elusive. Here, a comprehensive transcriptome analysis was conducted to explore the potential regulatory mechanism of anthocyanin biosynthesis in 'Red Zaosu' pear ( × ). Gene co-expression analysis and transcription factor mining identified 263 transcription factors, which accounted for 6.59% of the total number of transcription factors in the pear genome in two gene modules that are highly correlated with anthocyanin biosynthesis. Clustering, gene network modeling with STRING-DB, and local motif enrichment analysis (CentriMo) analysis suggested that PpPIF8 may play a role in anthocyanin biosynthesis. Furthermore, eight PIFs were identified in the pear genome, of which only was rapidly induced by light. Functional studies showed that PpPIF8 localizes in the nucleus and is preferentially expressed in the tissue of higher levels of anthocyanin. The overexpression of PpPIF8 in pear peel and pear calli promotes anthocyanin biosynthesis and upregulates the expression of anthocyanin biosynthesis genes. Yeast-one hybrid and transgenic analyses indicated that PpPIF8 binds to the promoter to induce expression. The positive effect of PpPIF8 on anthocyanin biosynthesis is different from previously identified negative regulators of PyPIF5 and MdPIF7 in pear and apple. Taken together, our data not only provide a comprehensive view of transcription events during the coloration of pear peel, but also resolved the regulatory role of PpPIF8 in the anthocyanin biosynthesis pathway.

摘要

红皮梨因其外观诱人、富含花青素而深受人们喜爱。然而,红皮梨中花青素生物合成的分子基础仍不清楚。在这里,我们进行了全面的转录组分析,以探讨‘红早酥’梨( × )中花青素生物合成的潜在调控机制。基因共表达分析和转录因子挖掘鉴定了 263 个转录因子,占梨基因组中总转录因子的 6.59%,这两个基因模块与花青素生物合成高度相关。聚类、基于 STRING-DB 的基因网络建模和局部 motif 富集分析(CentriMo)分析表明,PpPIF8 可能在花青素生物合成中发挥作用。此外,在梨基因组中鉴定出了 8 个 PIFs,其中只有 被光迅速诱导。功能研究表明,PpPIF8 定位于细胞核,在花青素含量较高的组织中优先表达。在梨果皮和梨愈伤组织中过表达 PpPIF8 可促进花青素生物合成,并上调花青素生物合成基因的表达。酵母单杂交和转基因分析表明,PpPIF8 结合到 启动子上诱导 表达。PpPIF8 对花青素生物合成的正向作用不同于先前在梨和苹果中鉴定的负调控因子 PyPIF5 和 MdPIF7。总之,我们的数据不仅提供了梨果皮着色过程中转录事件的全面视图,还解析了 PpPIF8 在花青素生物合成途径中的调控作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c21/9099880/12595fdc713d/ijms-23-04798-g001.jpg

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