Nomura Taiji, Nasuda Shuhei, Kawaura Kanako, Ogihara Yasunari, Kato Nobuhiko, Sato Fumihiko, Kojima Toshio, Toyoda Atsushi, Iwamura Hajime, Endo Takashi R
Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto, 606-8502, Japan.
Theor Appl Genet. 2008 Feb;116(3):373-81. doi: 10.1007/s00122-007-0675-1. Epub 2007 Nov 27.
Common wheat (2n=6x=42, genome formula AABBDD) accumulates benzoxazinones (Bxs) as defensive compounds. There are five Bx biosynthetic genes (TaBx1-TaBx5), and their homoeologous alleles are located on all three homoeologous chromosomes of the A, B and D genomes. Here the molecular structures of the TaBx3 and TaBx4 loci, both of which are located on chromosomes 5A, 5B and 5D, were revealed by sequencing transformation-competent artificial chromosome (TAC) clones. In all homoeologous chromosomes, TaBx3 existed downstream of TaBx4 in a tail-to-head manner, and the two genes were separated from each other by 9.0 kb in 5A, 7.3 kb in 5B and 11.3 kb in 5D. Among the three homoeologs of TaBx3 and TaBx4, the promoter sequences were less conserved than the coding sequences. The promoter sequences of TaBx3 and TaBx4 were highly similar to those of their respective orthologs in the diploid progenitors of common wheat, but were not similar to those of the maize orthologs. Sequence similarity was found between the TaBx3 and TaBx4 coding sequences, but not between their promoter sequences despite their similar transcription pattern at the seedling stage. Some putative cis-elements were found to be shared by all TaBx3 and TaBx4 promoter regions. These results imply that stage-specific transcription of TaBx3 and TaBx4 is not controlled by global sequence similarity of their promoters but by some essential cis-elements. The promoter activity measured by transient assays in wheat protoplasts was similar among the three homoeologs of TaBx3 and TaBx4 in spite of their differential transcript levels in wheat seedlings.
普通小麦(2n = 6x = 42,基因组公式为AABBDD)积累苯并恶嗪酮(Bxs)作为防御性化合物。有五个Bx生物合成基因(TaBx1 - TaBx5),它们的同源等位基因位于A、B和D基因组的所有三条同源染色体上。在此,通过对具备转化能力的人工染色体(TAC)克隆进行测序,揭示了位于5A、5B和5D染色体上的TaBx3和TaBx4位点的分子结构。在所有同源染色体中,TaBx3以尾对首的方式存在于TaBx4的下游,这两个基因在5A中相隔9.0 kb,在5B中相隔7.3 kb,在5D中相隔11.3 kb。在TaBx3和TaBx4的三个同源基因中,启动子序列的保守性低于编码序列。TaBx3和TaBx4的启动子序列与其在普通小麦二倍体祖先中各自的直系同源序列高度相似,但与玉米直系同源序列不相似。尽管TaBx3和TaBx4在幼苗期转录模式相似,但其编码序列之间存在序列相似性,而启动子序列之间不存在。发现一些推定的顺式元件在所有TaBx3和TaBx4启动子区域中共享。这些结果表明,TaBx3和TaBx4的阶段特异性转录不是由其启动子的整体序列相似性控制,而是由一些必需的顺式元件控制。尽管TaBx3和TaBx4在小麦幼苗中的转录水平存在差异,但通过小麦原生质体瞬时测定法测得的启动子活性在这三个同源基因中相似。