Utsugi Shigeko, Nakamura Shingo, Noda Kazuhiko, Maekawa Masahiko
Research Institute for Bioresources, Okayama University, Kurashiki, Okayama, Japan.
Genes Genet Syst. 2008 Apr;83(2):153-66. doi: 10.1266/ggs.83.153.
Viviparous 1 (Vp1) of maize is known to encode a transcription factor VP1 that controls seed germination. Hexaploid wheat possesses three Vp1 homoeologues (TaVp1): TaVp-A1, TaVp-B1 and TaVp-D1. In this study, we attempted to characterize the molecular properties of TaVp1 in a highly dormant wheat cultivar, Minamino-komugi (Minamino). The seeds of Minamino showed much higher sensitivity to the inhibitory effect of ABA on germination than those of non-dormant cultivars, Sanin-1 and Tozan-18. The sequence analyses of cDNAs also revealed that some of TaVp-A1 transcripts and TaVp-D1 transcripts were spliced incorrectly, presumably resulting in production of truncated or deleted proteins. Most TaVp-B1 transcripts were spliced correctly, but some had an additional 3-bp (AAG) insertion in the B3 domain, which may not affect their function. RT-PCR analyses showed that TaVp1 was highly expressed in Minamino embryos in maturing seeds but much less in roots and leaves of seedlings. The level of TaVp1 mRNA was high when the embryos were treated with ABA but markedly decreased in water-imbibed mature embryos whose dormancy had been broken. Expression analyses of the individual homoeologues showed that the level of TaVp-A1 transcripts was highest in embryos of DAP 20 but much lower in the matured embryos. TaVp-B1 was highly expressed in developing and maturing seed embryos, while TaVp-D1 mRNA existed at lower levels in developing embryos but increased as the seeds were matured. These results suggest that the majority of TaVp1, especially TaVp-B1, are properly spliced and may function as a transcription factor playing an important role on dormancy in Minamino. By employing an efficient transient expression system using diploid wheat seeds, we confirmed the dual function of TaVP-B1: the activation of Em expression and the repression of alpha-amylase expression.
已知玉米的胎生1(Vp1)编码一种控制种子萌发的转录因子VP1。六倍体小麦拥有三个Vp1同源基因(TaVp1):TaVp - A1、TaVp - B1和TaVp - D1。在本研究中,我们试图在高度休眠的小麦品种南之庄小麦(Minamino - komugi,简称Minamino)中表征TaVp1的分子特性。与非休眠品种佐贺1号(Sanin - 1)和登仙18号(Tozan - 18)相比,Minamino的种子对脱落酸(ABA)抑制萌发的作用更为敏感。对cDNA的序列分析还表明,一些TaVp - A1转录本和TaVp - D1转录本存在错误剪接,推测这会导致截短或缺失蛋白的产生。大多数TaVp - B1转录本剪接正确,但有些在B3结构域中有一个额外的3碱基对(AAG)插入,这可能不影响其功能。逆转录聚合酶链反应(RT - PCR)分析表明,TaVp1在成熟种子的Minamino胚中高度表达,但在幼苗的根和叶中表达量低得多。当胚用ABA处理时,TaVp1的mRNA水平较高,但在休眠已被打破的吸胀成熟胚中显著下降。对各个同源基因的表达分析表明,TaVp - A1转录本水平在授粉后20天(DAP 20)的胚中最高,但在成熟胚中低得多。TaVp - B1在发育中和成熟的种子胚中高度表达,而TaVp - D1 mRNA在发育中的胚中水平较低,但随着种子成熟而增加。这些结果表明,大多数TaVp1,尤其是TaVp - B1,剪接正确,可能作为转录因子在Minamino的休眠中发挥重要作用。通过使用二倍体小麦种子的高效瞬时表达系统,我们证实了TaVP - B1的双重功能:激活Em表达和抑制α -淀粉酶表达。