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Acta Agron Sin ›› 2016, Vol. 42 ›› Issue (02): 170-179.doi: 10.3724/SP.J.1006.2016.00170

• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles     Next Articles

Molecular Cloning of ZmPP6C Gene and Its Expression Patterns in Response to Light and Stress Treatments in Maize (Zea mays L.)

YUAN Huan-Huan1,2,**,SUN Guang-Hua1,2,**,YAN Lei 2,GUO Lin2,FAN Xiao-Cong1,2,XIAO Yang3,MENG Fan-Hua2,SONG Mei-Fang2,4,ZHAN Ke-Hui1,YANG Qing-hua1,*, YANG Jian-Ping1,2,*   

  1. 1 College of Agronomy, Henan Agricultural University/Collaborative Innovation Center of Henan Grain Crops, Zhengzhou 450002, China; 2 Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China; 3 Graduate School, Chinese Academy of Agricultural Sciences, Beijing 100081, China; 4Beijing Radiation Center, Beijing 100875, China
  • Received:2015-08-27 Revised:2015-11-20 Online:2016-02-12 Published:2015-12-07
  • Supported by:

    This study was supported by the Natural Science Foundation (6151002), the Major Project of China on New Varieties of GMO Cultivation (2014ZX08010-002), the National Natural Science Foundation of China (31570268, 31170267) and the Agricultural Science and Technology Innovation Program (ASTIP) of CAAS.

Abstract:

PP6C is the catalytic subunits of Ser/Thr protein phosphatase 6 (PP6) gene, which plays important roles in auxin transport polarity, ABA (abscisic acid) signal transduction, flowering time control though light signaling pathway. To clarify structural characteristics of PP6C protein and the evolution relationships among plant PP6Chomologs, we cloned ZmPP6C gene by RT-PCR. The open reading frame (ORF) of ZmPP6C possesses 912 nucleotides and encodes 303 amino acid residues with one PP2Ac domain (the catalytic subunits of Ser/Thr protein phosphatase 2A). Phylogenetic analysis indicated that ZmPP6C belongs to the same branch with the PP6C of Sorghum bicolor, and shows high similarity to all PP6C proteins from other monocotyledons and dicotyledons. Further quantitative RT-PCR (qRT-PCR) assays indicated that ZmPP6C was highly expressed in leaf and lowly in stem, stamen, pulvinus, sheath, and pedical. ZmPP6C transcription abundances could respond to different light and circadian treatments (both long-day and short-day conditions), especially to the light transitions from the dark to far-red or red light condition. In addition, ZmPP6C transcription abundances were up-regulated by high osmosis, high salt and water logging. Our results suggested that ZmPP6C may be involved in light signaling pathway, flowering time control, and abiotic stress response in maize, and its roles in crop improvement are worthy of more exploration in the future.

Key words: Zea mays, ZmPP6C, Expression patterns, Phytochrome, Light signaling pathway, Abiotic stress

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