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杨树中六个基因的分子克隆、转录谱分析、亚细胞定位及miRNA结合位点分析

Molecular Cloning, Transcriptional Profiling, Subcellular Localization, and miRNA-Binding Site Analysis of Six Genes in Poplar.

作者信息

Zhao Meiqi, Xuan Lei, Qi Haoran, Shen Tengfei, Xu Meng

机构信息

Key Laboratory of Forest Genetics and Biotechnology of Ministry of Education, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China.

Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem, Sun Yat-Sen), Nanjing 210014, China.

出版信息

Plants (Basel). 2021 Jun 30;10(7):1338. doi: 10.3390/plants10071338.

Abstract

The SCL9 subfamily is a key member of the GRAS family that regulates plant development and stress responses. Nevertheless, the functional role of these genes in the growth and development of poplar still unclear. Here, we reported the six genes, which were found to be differentially expressed during poplar adventitious root formation. The full-length sequences of genes of 'Nanlin895' poplar ( × ) were cloned by the RACE technique All genes lacked introns. RT-qPCR revealed that genes displayed a dynamic expression pattern in the adventitious root of poplar, according to RT-qPCR data. A series of comprehensive genes characteristics analysis were carried out for six genes by bioinformation. Meanwhile, transient expression analysis of the protoplasts showed that all the PeSCL9 proteins were localized in the nucleus. In addition, the degradome and sRNA of 'Nanlin895' poplar in combination were used to predict miRNAs that regulate . It was found that miR396a and miR396c may affect expression via cleavage, which was further verified by a transient expression experiment in protoplasts. Overall, the development of poplar adventitious root and other tissues was closely related to these six genes, and they serve as a starting point for further research into the mechanisms regulating poplar growth and development.

摘要

SCL9亚家族是GRAS家族的关键成员,调控植物发育和胁迫反应。然而,这些基因在杨树生长发育中的功能作用仍不清楚。在此,我们报道了6个基因,发现它们在杨树不定根形成过程中差异表达。采用RACE技术克隆了‘南林895’杨树(×)基因的全长序列。所有基因均无内含子。根据RT-qPCR数据,RT-qPCR显示这些基因在杨树不定根中呈现动态表达模式。通过生物信息学对6个基因进行了一系列全面的基因特征分析。同时,原生质体的瞬时表达分析表明,所有PeSCL9蛋白均定位于细胞核。此外,结合‘南林895’杨树的降解组和小RNA预测调控的miRNA。发现miR396a和miR396c可能通过切割影响表达,这在原生质体的瞬时表达实验中得到进一步验证。总体而言,杨树不定根和其他组织的发育与这6个基因密切相关,它们是进一步研究杨树生长发育调控机制的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a83f/8309000/89d7c3da1dab/plants-10-01338-g001.jpg

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