Expression Characteristic of TaPDC-E1α Gene and Its regulatory Enzymes Gene in Male Sterile Line of Wheat

Q3 Agricultural and Biological Sciences Acta Agronomica Sinica Pub Date : 2011-04-01 DOI:10.1016/S1875-2780(11)60017-5
Long-Yu ZHANG, Lei YUAN, Shu-Ling YANG, Gai-Sheng ZHANG, Jun-Sheng WANG, Yu-Long SONG, Na NIU, Shou-Cai MA
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引用次数: 5

Abstract

To understand the mechanism of male sterility induced by gametocide SQ-1 in wheat (Triticum aestivum L.), TaPDC-E1α gene was isolated using silcon cloning technique. The open reading frame of this gene is 1401 bp in length, putatively encoding 388 amino acid residues. This gene possesses the conserved TPP domains. Two potential phosphorylation sites of serine residues might be present in the TaPDC-E1α protein of wheat. According to semiquantitative reverse transcription polymerase chain reaction (RT-PCR) analysis, the expression levels of TaPDC-E1α in the physiological and genetic male sterile lines were lower than those in the fertile lines. Compared with the fertile lines, the expression of PDK was obviously down-regulated in the physiological male sterile line induced by SQ-1. However, PDK gene was highly expressed in the genetic male sterile lines. The expression levels of PDP gene were similar in the fertile and the male-sterile lines. These results suggest that the pathway of energy metabolism in the SQ-1 induced sterile line is more susceptible than that of the genetic male-sterile line. The upstream signal mechanism of mediating PDK gene may be inconsistent between the male-sterile line induced by SQ-1 and the genetic male-sterile line.

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小麦雄性不育系TaPDC-E1α基因及其调控酶基因的表达特征
为了解配子体杀菌剂SQ-1诱导小麦雄性不育的机制,采用硅克隆技术分离了TaPDC-E1α基因。该基因的开放阅读框长度为1401 bp,推测编码388个氨基酸残基。该基因具有保守的TPP结构域。小麦TaPDC-E1α蛋白中可能存在两个潜在的丝氨酸残基磷酸化位点。根据半定量反转录聚合酶链反应(RT-PCR)分析,TaPDC-E1α在雄性生理和遗传不育系中的表达水平低于可育系。与可育系相比,SQ-1诱导的生理雄性不育系中PDK的表达明显下调。而PDK基因在遗传雄性不育系中高表达。PDP基因在可育系和不育系中的表达水平相似。这些结果表明,SQ-1诱导不育系的能量代谢途径比遗传雄性不育系更敏感。SQ-1诱导的雄性不育系与遗传雄性不育系之间介导PDK基因的上游信号机制可能不一致。
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30 weeks
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