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作物学报 ›› 2011, Vol. 37 ›› Issue (04): 620-628.doi: 10.3724/SP.J.1006.2011.00620

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

小麦雄性不育系中TaPDC-E1a及其调节酶基因的表达特征

张龙雨,袁蕾,杨书玲,张改生*,王俊生,宋瑜龙,赵卓军,牛娜,马守才   

  1. 西北农林科技大学 / 陕西省作物杂种优势研究与利用重点实验室 / 小麦育种教育部工程研究中心，陕西杨凌 712100
  • 收稿日期:2010-09-25 修回日期:2011-01-06 出版日期:2011-04-12 网络出版日期:2011-02-24
  • 通讯作者: 张改生, E-mail: zhanggsh@public.xa.sn.cn, Tel: 029-87092152
  • 基金资助:

    本研究由国家高技术研究发展计划(863计划)重大专项(2009AA101102), 国家自然科学基金项目(31071477), 高等学校博士学科点专项科研基金(20090204110024)和西北农林科技大学拔尖人才支持计划项目资助。

Expression Characteristic on TaPDC-E1a Gene and Its regulatory Enzymes Gene in Male Sterile Line of Wheat (Triticum aestivum)

ZHANG Long-Yu,YUAN Lei,YANG Shu-Ling,ZHANG Gai-Sheng*,WANG Jun-Sheng,SONG Yu-Long,ZHAO Zhuo-Jun,NIU Na,MA Shou-Cai   

  1. Northwest A&F University/Key Laboratory of Crop Heterosis of Shaanxi Province / Wheat Breeding Engineering Research Center, Ministry of Education, Yangling 712100, China
  • Received:2010-09-25 Revised:2011-01-06 Published:2011-04-12 Published online:2011-02-24
  • Contact: 张改生, E-mail: zhanggsh@public.xa.sn.cn, Tel: 029-87092152

PDF

995

被引次数

24

摘要： 为进一步研究杀雄剂SQ-1诱导小麦雄性不育的机制，采用电子克隆的方法分离TaPDC-E1a基因，并利用半定量RT-PCR技术分析该基因及其调节酶基因PDK和PDP的表达特性。结果表明，TaPDC-E1a基因编码388个氨基酸，具有TPP保守结构域，可能存在2个丝氨酸磷酸化位点；与可育系相比，TaPDC-E1a基因在生理型不育系和遗传型不育系中表达下调；PDK基因在生理型不育系中表达下调，而在遗传型不育系中表达上调；PDP基因在可育系及不育系中的表达趋势无明显变化。表明经杀雄剂SQ-1诱导形成的生理型不育系在败育过程中其能量代谢途径更容易受到影响，推测对PDK基因进行调节的上游信号机制在小麦生理型不育系与遗传型不育系中可能不一致。

关键词: 杀雄剂SQ-1, TaPDC-E1a, PDK, PDP, 磷酸化位点

Abstract: To deeply study the mechanism of male sterility induced by gametocide SQ-1 in wheat (Triticum aestivum L.), we isolated TaPDC-E1a gene using silcon cloning technique. The open reading frame of this gene is 1 401 bp in length, putatively encoding 388 amino acids. This gene possesses the conserved TPP domains. Two potential phosphorylation sites of serine residues might be present in the TaPDC-E1a protein of wheat. According to semi-quantitative RT-PCR analysis, the expression levels of TaPDC-E1a in the physiological and genetic male sterile lines were lower than those in fertile lines. Compared with 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 fertile and male-sterile lines. These results suggest that the pathway of energy metabolism of sterile line induced by SQ-1 is more susceptible than that of genetic male-sterile line.The upstream signal mechanism of mediating PDK gene may be inconsistent between male-sterile line induced bySQ-1 and genetic male-sterile line.

Key words: Wheat, gametocide SQ-1, TaPDC-E1a, PDK, PDP, Phosphorylation site

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