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拟南芥MYB26/雄性不育35调控药室内壁的次生加厚,对花药开裂至关重要。

Arabidopsis MYB26/MALE STERILE35 regulates secondary thickening in the endothecium and is essential for anther dehiscence.

作者信息

Yang Caiyun, Xu Zhengyao, Song Jie, Conner Katie, Vizcay Barrena Gema, Wilson Zoe A

机构信息

Plant Sciences Division, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough, Leicstershire LE12 5RD, United Kingdom.

出版信息

Plant Cell. 2007 Feb;19(2):534-48. doi: 10.1105/tpc.106.046391. Epub 2007 Feb 28.

Abstract

The Arabidopsis thaliana MYB26/MALE STERILE35 (MS35) gene is critical for the development of secondary thickening in the anther endothecium and subsequent dehiscence. MYB26 is localized to the nucleus and regulates endothecial development and secondary thickening in a cell-specific manner in the anther. MYB26 expression is seen in anthers and also in the style and nectaries, although there is no effect on female fertility in the ms35 mutant. MYB26 expression in anthers occurs early during endothecial development, with maximal expression during pollen mitosis I and bicellular stages, indicating a regulatory role in specifying early endothecial cell development. Overexpression of MYB26 results in ectopic secondary thickening in both Arabidopsis and tobacco (Nicotiana tabacum) plants, predominantly within the epidermal tissues. MYB26 regulates a number of genes linked to secondary thickening, including IRREGULAR XYLEM1 (IRX1), IRX3, IRX8, and IRX12. Changes in expression were also detected in two NAC domain genes, NAC SECONDARY WALL-PROMOTING FACTOR1 (NST1) and NST2, which have been linked to secondary thickening in the anther endothecium. These data indicate that MYB26 regulates NST1 and NST2 expression and in turn controls the process of secondary thickening. Therefore, MYB26 appears to function in a regulatory role involved in determining endothecial cell development within the anther and acts upstream of the lignin biosynthesis pathway.

摘要

拟南芥MYB26/雄性不育35(MS35)基因对于花药内壁次生加厚及随后的开裂发育至关重要。MYB26定位于细胞核,并以细胞特异性方式调节花药内壁的发育和次生加厚。虽然ms35突变体对雌性育性没有影响,但在花药以及花柱和蜜腺中均可见MYB26的表达。MYB26在花药内壁发育早期表达,在花粉有丝分裂I期和双细胞期表达量最高,表明其在确定早期内壁细胞发育过程中具有调节作用。在拟南芥和烟草(Nicotiana tabacum)植株中,MYB26的过表达都会导致异位次生加厚,主要发生在表皮组织中。MYB26调节多个与次生加厚相关的基因,包括不规则木质部1(IRX1)、IRX3、IRX8和IRX12。在两个NAC结构域基因,即与花药内壁次生加厚相关的NAC次生壁促进因子1(NST1)和NST2中也检测到了表达变化。这些数据表明,MYB26调节NST1和NST2的表达,进而控制次生加厚过程。因此,MYB26似乎在确定花药内壁细胞发育的调节作用中发挥功能,并在木质素生物合成途径的上游起作用。

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