Jia Qi-Shi, Zhu Jun, Xu Xiao-Feng, Lou Yue, Zhang Zhan-Lin, Zhang Zhi-Ping, Yang Zhong-Nan
College of Life and Environment Sciences, Shanghai Normal University, Shanghai, 200234, China College of Agriculture, Henan University of Science and Technology, Luoyang, 471003, China.
College of Life and Environment Sciences, Shanghai Normal University, Shanghai, 200234, China.
Mol Plant. 2014 Oct 20. doi: 10.1093/mp/ssu114.
Nexine is a conserved layer of the pollen wall. We previously reported that the nexine layer is absent in the knockout mutant of TRANSPOSABLE ELEMENT SILENCING VIA AT-HOOK (TEK). In this work, we characterized the molecular function of TEK in pollen development and identified direct targets of TEK, Arabinogalactan proteins (AGPs), which are responsible for nexine formation. Electrophoretic mobility shift assay (EMSA) showed that TEK can directly bind to the nuclear matrix attachment region (MAR). Phenotypic similarity between tek and the TEK-SRDX transgenic lines indicated that TEK plays a role in transcriptional activation in anther development. Microarray analysis identified a total of 661 genes downstream of TEK, including four genes encoding AGPs, AGP6, AGP11, AGP23 and AGP40. Chromatin immunoprecipitation (ChIP) followed by PCR analysis using the FLAG-tagged TEK complement lines suggested that TEK is enriched in the promoters of these four genes. EMSA further confirmed that TEK binds to the AGP6 promoter. The expression of AGP6 driven by the TEK promoter in tek can partially rescue both nexine formation and plant fertility. These results show that TEK directly regulates AGPs expression in the anther. It is proposed that glycoproteins are an essential component of the nexine layer in the pollen wall.
外壁内层是花粉壁的一个保守层。我们之前报道过,通过AT钩转座元件沉默(TEK)的基因敲除突变体中不存在外壁内层。在这项研究中,我们对TEK在花粉发育中的分子功能进行了表征,并鉴定出TEK的直接靶标——阿拉伯半乳聚糖蛋白(AGP),其负责外壁内层的形成。电泳迁移率变动分析(EMSA)表明,TEK能直接结合到核基质附着区(MAR)。tek与TEK-SRDX转基因系之间的表型相似性表明,TEK在花药发育的转录激活中发挥作用。微阵列分析共鉴定出661个TEK下游基因,包括四个编码AGP的基因,即AGP6、AGP11、AGP23和AGP40。使用带有FLAG标签的TEK互补系进行染色质免疫沉淀(ChIP),随后进行PCR分析,结果表明TEK在这四个基因的启动子区域富集。EMSA进一步证实,TEK能结合到AGP6启动子上。由TEK启动子驱动的AGP6在tek中的表达能够部分挽救外壁内层的形成和植株育性。这些结果表明,TEK直接调控花药中AGP的表达。我们推测糖蛋白是花粉壁外壁内层的重要组成部分。