Wei Yun-Liang, Li Jia-Na, Lu Jun, Tang Zhang-Lin, Pu Dong-Chun, Chai You-Rong
Chongqing Rapeseed Engineering Research Center, Southwest University, 216 Tiansheng Road, Beibei, Chongqing 400716, People's Republic of China.
Mol Biol Rep. 2007 Jun;34(2):105-20. doi: 10.1007/s11033-006-9024-8. Epub 2006 Nov 18.
Three members of Brassica napus TRANSPARENT TESTA 2 (BnTT2) gene family encoding potential R2R3-MYB regulatory proteins of proanthocyanidin biosynthesis were isolated. BnTT2-1, BnTT2-2, and BnTT2-3 are 1102 bp with two introns, and have a 938-bp full-length cDNA with a 260 amino acid open reading frame. They share 98.2-99.3% nucleotide and 96.5-98.5% amino acid identities to each other, and are orthologous to Arabidopsis thaliana TT2 (AtTT2) with 74.1-74.8% nucleotide and 71.1-71.8% amino acid identities. An mRNA type of BnTT2-2 was found to contain unspliced intron 2 and encode a premature protein. They all have an alternative polyadenylation site. BnTT2-1 and BnTT2-3 also have an alternative transcription initiation site. Aligned with AtTT2, their 5' untranslated regions (UTRs) are astonishingly conserved, and two conserved regions were also found in their 3' UTRs. Oligonucleotide deletion leads to double-start codons of them. Resembling AtTT2, BnTT2 proteins are nuclear-located R2R3-MYB proteins containing predicted DNA-binding sites, bHLH interaction residues, and transcription activation domains. Southern blot indicated that there might be three BnTT2 members in B. napus, lower than triplication-based prediction. Semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) revealed that the expression of BnTT2-2 is mostly like AtTT2 with intensive expression in young seeds, but it is also expressed in root in which AtTT2 has no expression. BnTT2-1 shows lower tissue specificity and transcription levels, whereas BnTT2-3 is the lowest. Comparative cloning and RT-PCR indicated that seed color near-isogenic lines L1 and L2 have equivalent BnTT2 genes, and the yellow seed color in L2 might be caused by locus/loci other than BnTT2. Our results lay the basis for further investigating the regulatory mechanism of BnTT2 genes in flavonoid pathway and for transgenic creation of novel yellow-seeded B. napus stocks.
分离出了甘蓝型油菜透明种皮2(BnTT2)基因家族的三个成员,它们编码原花青素生物合成中潜在的R2R3-MYB调控蛋白。BnTT2-1、BnTT2-2和BnTT2-3全长1102 bp,含两个内含子,具有一个938 bp的全长cDNA,开放阅读框为260个氨基酸。它们彼此之间的核苷酸同源性为98.2 - 99.3%,氨基酸同源性为96.5 - 98.5%,与拟南芥TT2(AtTT2)是直系同源基因,核苷酸同源性为74.1 - 74.8%,氨基酸同源性为71.1 - 71.8%。发现BnTT2-2的一种mRNA类型含有未剪接的内含子2,并编码一种早熟蛋白。它们都有一个可变聚腺苷酸化位点。BnTT2-1和BnTT2-3也有一个可变转录起始位点。与AtTT2比对,它们的5'非翻译区(UTR)惊人地保守,在其3'UTR中也发现了两个保守区域。寡核苷酸缺失导致它们出现双起始密码子。与AtTT2相似,BnTT2蛋白是定位于细胞核的R2R3-MYB蛋白,含有预测的DNA结合位点、bHLH相互作用残基和转录激活结构域。Southern杂交表明甘蓝型油菜中可能有三个BnTT2成员,低于基于三倍化的预测。半定量逆转录-聚合酶链反应(RT-PCR)显示,BnTT2-2的表达模式与AtTT2最为相似,在幼嫩种子中大量表达,但在AtTT2不表达的根中也有表达。BnTT2-1的组织特异性和转录水平较低,而BnTT2-3最低。比较克隆和RT-PCR表明,种子颜色近等基因系L1和L2具有等同的BnTT2基因,L2中的黄色种子颜色可能是由BnTT2以外的一个或多个基因座引起的。我们的结果为进一步研究BnTT2基因在类黄酮途径中的调控机制以及创建新型黄色种子甘蓝型油菜转基因材料奠定了基础。