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院士发表Plant Cell文章解析miRNAs

来自中科院上海植物生理生态研究所植物分子遗传国家重点实验室,加拿大哥伦比亚大学的研究人员发现miR156-靶基因SPL调控拟南芥表皮毛的分布。这一研究成果公布在植物科学研究权威期刊PlantCell上。

领导这一研究的是中科院上海植物生理生态研究所的陈晓亚研究员,他2005年当选为中国科学院院士。1982年毕业于南京大学生物学系,1985年在英国里丁(Reading)大学获博士学位。现任植物生理生态研究所所长、植物分子遗传国家重点实验室主任等。

 

 

植物表皮毛覆盖于植物地上组织的表面,具有多种不同的生理功能,有些还具有重要的经济价值,如棉纤维。表皮毛的分布受到时空调控。模式植物拟南芥在营养发育时期,表皮毛主要生长于莲座叶的近轴面;而当植物进入生殖发育期,表皮毛的数量随着花序轴的延伸而减少,直至花器官(除花萼外)基本无毛。这一分布特征表明表皮毛发育的调控与植物发育的时相转换有着密不可分的关系。

在这篇文章中,研究人员发现miR156-靶基因SPL调控拟南芥表皮毛的分布,受miR156调控的SPLs基因家族是连接植物发育进程和表皮毛发育的桥梁。

SPL (SQUMOSA PROMOTER BINDING PROTEINLIKE)基因编码重要的转录因子。SPL家族的大部分成员是microRNA156的靶基因,它们在植物进入生殖生长期的时相转换过程中起关键的调控作用。过量表达miR156(p35S::MIR156f)导致SPLs水平降低,花序轴上部和花柄器官均出现异位毛生长;反之SPL基因高表达导致茎杆上表皮毛数量下降甚至光滑无毛。在拟南芥表皮毛发育过程中,GL1-GL3-TTG1蛋白复合体正调控表皮毛发育,而棉纤维发育也由类似复合体控制。

另一类单MYB转录因子TRICHOMELESS 1 (TCL1) 和TRIPTYCHON(TRY)在蛋白水平上与GL1竞争结合GL3,从而阻断表皮毛发育。研究表明,SPL9通过直接结合TCL1和TRY的启动子来激活这两个负调控因子,抑制表皮毛生长。上述结果表明,受miR156调控的SPLs基因家族是连接植物发育进程和表皮毛发育的桥梁。棉花植物中miR156的含量很高,其对棉纤维发育的调控作用值得进一步探讨。
 

原文摘要:

Temporal Control of Trichome Distribution byMicroRNA156-Targeted SPL Genes in Arabidopsis thaliana[W],[OA]

The production and distribution of plant trichomes is temporallyand spatially regulated. After entering into the flowering stage,Arabidopsis thaliana plants have progressively reduced numbers oftrichomes on the inflorescence stem, and the floral organs arenearly glabrous. We show here that SQUAMOSA PROMOTER BINDINGPROTEIN LIKE (SPL) genes, which define an endogenous floweringpathway and are targeted by microRNA 156 (miR156), temporallycontrol the trichome distribution during flowering. Plantsoverexpressing miR156 developed ectopic trichomes on the stem andfloral organs. By contrast, plants with elevated levels of SPLsproduced fewer trichomes. During plant development, the increase inSPL transcript levels is coordinated with the gradual loss oftrichome cells on the stem. The MYB transcription factor genesTRICHOMELESS1 (TCL1) and TRIPTYCHON (TRY) are negative regulatorsof trichome development. We show that SPL9 directly activates TCL1and TRY expression through binding to their promoters and that thisactivation is independent of GLABROUS1 (GL1). The phytohormonescytokinin and gibberellin were reported to induce trichomeformation on the stem and inflorescence via the C2H2 transcriptionfactors GIS, GIS2, and ZFP8, which promote GL1 expression. We showthat the GIS-dependent pathway does not affect the regulation ofTCL1 and TRY by miR156-targeted SPLs, represented by SPL9. Theseresults demonstrate that the miR156-regulated SPLs establish adirect link between developmental programming and trichomedistribution.