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Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene

Phosphoenolpyruvate carboxylase (PEPC) is known to play a key role in the initial fixation of CO(2) in C4 photosynthesis. The PEPC gene from sugarcane (a C4 plant) was introduced into indica rice (Hang2), a process mediated by Agrobacterium tumefaciens. Integration patterns and copy numbers of the g...

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Autores principales: Lian, Ling, Wang, Xiaowei, Zhu, Yongsheng, He, Wei, Cai, Qiuhua, Xie, Huaan, Zhang, Muqing, Zhang, Jianfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968443/
https://www.ncbi.nlm.nih.gov/pubmed/24469712
http://dx.doi.org/10.1007/s11033-014-3070-4
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author Lian, Ling
Wang, Xiaowei
Zhu, Yongsheng
He, Wei
Cai, Qiuhua
Xie, Huaan
Zhang, Muqing
Zhang, Jianfu
author_facet Lian, Ling
Wang, Xiaowei
Zhu, Yongsheng
He, Wei
Cai, Qiuhua
Xie, Huaan
Zhang, Muqing
Zhang, Jianfu
author_sort Lian, Ling
collection PubMed
description Phosphoenolpyruvate carboxylase (PEPC) is known to play a key role in the initial fixation of CO(2) in C4 photosynthesis. The PEPC gene from sugarcane (a C4 plant) was introduced into indica rice (Hang2), a process mediated by Agrobacterium tumefaciens. Integration patterns and copy numbers of the gene was confirmed by DNA blot analysis. RT-PCR and western blotting results showed that the PEPC gene was expressed at both the mRNA and protein levels in the transgenic lines. Real-time PCR results indicated that expression of the sugarcane PEPC gene occurred mostly in green tissues and changed under high temperature and drought stress. All transgenic lines showed higher PEPC enzyme activities compared to the untransformed controls, with the highest activity (11.1 times higher than the controls) being observed in the transgenic line, T34. The transgenic lines also exhibited higher photosynthetic rates. The highest photosynthetic rate was observed in the transgenic line, T54 (22.3 μmol m(−2) s(−1); 24.6 % higher than that in non-transgenic plants) under high-temperature conditions. Furthermore, the filled grain and total grain numbers for transgenic lines were higher than those for non-transgenic plants, but the grain filling (%) and 1,000-grain weights of all transgenic lines remained unchanged. We concluded that over-expression of the PEPC gene from sugarcane in indica rice (Hang2) resulted in higher PEPC enzyme activities and higher photosynthesis rates under high-temperature conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11033-014-3070-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-39684432014-03-28 Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene Lian, Ling Wang, Xiaowei Zhu, Yongsheng He, Wei Cai, Qiuhua Xie, Huaan Zhang, Muqing Zhang, Jianfu Mol Biol Rep Article Phosphoenolpyruvate carboxylase (PEPC) is known to play a key role in the initial fixation of CO(2) in C4 photosynthesis. The PEPC gene from sugarcane (a C4 plant) was introduced into indica rice (Hang2), a process mediated by Agrobacterium tumefaciens. Integration patterns and copy numbers of the gene was confirmed by DNA blot analysis. RT-PCR and western blotting results showed that the PEPC gene was expressed at both the mRNA and protein levels in the transgenic lines. Real-time PCR results indicated that expression of the sugarcane PEPC gene occurred mostly in green tissues and changed under high temperature and drought stress. All transgenic lines showed higher PEPC enzyme activities compared to the untransformed controls, with the highest activity (11.1 times higher than the controls) being observed in the transgenic line, T34. The transgenic lines also exhibited higher photosynthetic rates. The highest photosynthetic rate was observed in the transgenic line, T54 (22.3 μmol m(−2) s(−1); 24.6 % higher than that in non-transgenic plants) under high-temperature conditions. Furthermore, the filled grain and total grain numbers for transgenic lines were higher than those for non-transgenic plants, but the grain filling (%) and 1,000-grain weights of all transgenic lines remained unchanged. We concluded that over-expression of the PEPC gene from sugarcane in indica rice (Hang2) resulted in higher PEPC enzyme activities and higher photosynthesis rates under high-temperature conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11033-014-3070-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2014-01-29 2014 /pmc/articles/PMC3968443/ /pubmed/24469712 http://dx.doi.org/10.1007/s11033-014-3070-4 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Lian, Ling
Wang, Xiaowei
Zhu, Yongsheng
He, Wei
Cai, Qiuhua
Xie, Huaan
Zhang, Muqing
Zhang, Jianfu
Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene
title Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene
title_full Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene
title_fullStr Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene
title_full_unstemmed Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene
title_short Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene
title_sort physiological and photosynthetic characteristics of indica hang2 expressing the sugarcane pepc gene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968443/
https://www.ncbi.nlm.nih.gov/pubmed/24469712
http://dx.doi.org/10.1007/s11033-014-3070-4
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