Suppr超能文献

CROWN ROOTLESS1 以一种松弛的特异性结合 DNA,并激活 OsROP 和 OsbHLH044 基因,这些基因参与水稻冠根的形成。

CROWN ROOTLESS1 binds DNA with a relaxed specificity and activates OsROP and OsbHLH044 genes involved in crown root formation in rice.

机构信息

UMR DIADE, Université de Montpellier, IRD, CIRAD, 911 Avenue Agropolis, 34394, Montpellier cedex 5, France.

Laboratoire Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRAE, INRIA, Lyon, 69007, France.

出版信息

Plant J. 2022 Jul;111(2):546-566. doi: 10.1111/tpj.15838. Epub 2022 Jul 9.

Abstract

In cereals, the root system is mainly composed of post-embryonic shoot-borne roots, named crown roots. The CROWN ROOTLESS1 (CRL1) transcription factor, belonging to the ASYMMETRIC LEAVES2-LIKE/LATERAL ORGAN BOUNDARIES DOMAIN (ASL/LBD) family, is a key regulator of crown root initiation in rice (Oryza sativa). Here, we show that CRL1 can bind, both in vitro and in vivo, not only the LBD-box, a DNA sequence recognized by several ASL/LBD transcription factors, but also another not previously identified DNA motif that was named CRL1-box. Using rice protoplast transient transactivation assays and a set of previously identified CRL1-regulated genes, we confirm that CRL1 transactivates these genes if they possess at least a CRL1-box or an LBD-box in their promoters. In planta, ChIP-qPCR experiments targeting two of these genes that include both a CRL1- and an LBD-box in their promoter show that CRL1 binds preferentially to the LBD-box in these promoter contexts. CRISPR/Cas9-targeted mutation of these two CRL1-regulated genes, which encode a plant Rho GTPase (OsROP) and a basic helix-loop-helix transcription factor (OsbHLH044), show that both promote crown root development. Finally, we show that OsbHLH044 represses a regulatory module, uncovering how CRL1 regulates specific processes during crown root formation.

摘要

在谷类作物中,根系主要由胚后茎生根组成,称为冠根。冠根缺失 1 型(CRL1)转录因子属于不对称叶片 2 样/LATERAL ORGAN BOUNDARIES DOMAIN(ASL/LBD)家族,是水稻(Oryza sativa)冠根起始的关键调节因子。在这里,我们表明,CRL1 不仅可以在体外和体内结合 LBD 盒,这是几个 ASL/LBD 转录因子识别的 DNA 序列,还可以结合另一个以前未识别的 DNA 基序,我们将其命名为 CRL1 盒。利用水稻原生质体瞬时转激活测定和一组先前鉴定的 CRL1 调节基因,我们证实如果这些基因的启动子中至少存在一个 CRL1 盒或 LBD 盒,CRL1 就可以转录激活这些基因。在体内,针对两个包含启动子中 CRL1 盒和 LBD 盒的这些基因的 ChIP-qPCR 实验表明,CRL1 在这些启动子环境中优先结合 LBD 盒。CRISPR/Cas9 靶向突变这两个 CRL1 调节基因,它们编码植物 Rho GTPase(OsROP)和碱性螺旋-环-螺旋转录因子(OsbHLH044),表明它们都促进冠根发育。最后,我们表明 OsbHLH044 抑制一个调节模块,揭示了 CRL1 如何在冠根形成过程中调节特定过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b0/9542200/308679a3cdc0/TPJ-111-546-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验