China-UK HUST-RRes Genetic Engineering and Genomics Joint Laboratory, The Genetic Engineering International Cooperation Base of Ministry of Science and Technology, College of Life Science and Technology, Huazhong University of Science and Technology, Luoyu Road 1037, Wuhan, 430074, China.
Mol Biol Rep. 2010 Oct;37(7):3351-61. doi: 10.1007/s11033-009-9922-7. Epub 2009 Dec 15.
Carotene desaturation, an essential step in the carotenoid biosynthesis pathway, is catalyzed by two carotene desaturases, phytoene desaturase (PDS) and ζ-carotene desaturase (ζ-carotene desaturase, ZDS). Full-length cDNAs designated TaPDS and TaZDS were cloned from wheat (Triticum aestivum cv. Chinese Spring) respectively, using the rapid amplification of cDNA ends (RACE) approach. The cDNA of TaPDS sequence was 2076 bp long, containing a 1731 bp open reading frame (ORF) which deduced protein having 576 amino acid residues with predicted molecular mass of 64.3 kDa and having a putative transit sequence for plastid targeting in the N-terminal region. While the cDNA sequence of TaZDS was 2150 bp long, contained an ORF sequence of 1707 bp, and encoded a putative protein of 568 amino acid residues with an estimated molecular mass of 62.5 kDa. Phylogenetic analysis demonstrated that TaPDS and TaZDS showed high homology with other PDSs and ZDSs in higher plant species, respectively. Moreover, sequences analysis also showed a high degree of conservation among plant PDSs and ZDSs. The deduced TaPDS and TaZDS protein both have the dinucleotide binding domain and conserved regions characteristic of other carotene desaturases. Analysis of the expression pattern of wheat TaPDS and TaZDS in different tissues revealed that the transcripts levels were higher in leaves and flowers petals, followed by in inflorescences, and were nearly absent in the roots and seeds. Southern analysis of genomic DNA indicated that the wheat TaPDS and TaZDS probably belong to a low-copy-number gene family.
类胡萝卜素的双键不饱和化是类胡萝卜素生物合成途径中的一个关键步骤,该过程由两种类胡萝卜素双键不饱和酶,即番茄红素脱饱和酶(PDS)和 ζ-胡萝卜素脱饱和酶(ζ-carotene desaturase,ZDS)催化。本研究采用快速扩增 cDNA 末端(RACE)方法,分别从小麦(Triticum aestivum cv. Chinese Spring)中克隆得到全长 cDNAs TaPDS 和 TaZDS。TaPDS cDNA 序列长 2076 bp,包含一个 1731 bp 的开放阅读框(ORF),编码一个含有 576 个氨基酸残基的蛋白质,预测分子量为 64.3 kDa,在 N 端具有质体靶向的假定转运序列。而 TaZDS cDNA 序列长 2150 bp,包含一个 1707 bp 的 ORF 序列,编码一个推测的 568 个氨基酸残基的蛋白质,估计分子量为 62.5 kDa。系统进化分析表明,TaPDS 和 TaZDS 分别与高等植物中的其他 PDS 和 ZDS 具有高度同源性。此外,序列分析还表明,植物 PDS 和 ZDS 之间具有高度的保守性。推测的 TaPDS 和 TaZDS 蛋白都具有二核苷酸结合结构域和其他类胡萝卜素双键不饱和酶的保守区域。对小麦 TaPDS 和 TaZDS 在不同组织中的表达模式进行分析表明,叶片和花瓣中的转录本水平较高,花序次之,而根和种子中几乎检测不到。基因组 DNA 的 Southern 分析表明,小麦 TaPDS 和 TaZDS 可能属于低拷贝数基因家族。