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Protein body formation in stable transgenic tobacco expressing elastin-like polypeptide and hydrophobin fusion proteins.

Identifieur interne : 000452 ( Main/Exploration ); précédent : 000451; suivant : 000453

Protein body formation in stable transgenic tobacco expressing elastin-like polypeptide and hydrophobin fusion proteins.

Auteurs : Sonia P. Gutiérrez [Canada] ; Reza Saberianfar ; Susanne E. Kohalmi ; Rima Menassa

Source :

RBID : pubmed:23663656

Descripteurs français

English descriptors

Abstract

BACKGROUND

Plants are recognized as an efficient and inexpensive system to produce valuable recombinant proteins. Two different strategies have been commonly used for the expression of recombinant proteins in plants: transient expression mediated by Agrobacterium; or stable transformation of the plant genome. However, the use of plants as bioreactors still faces two main limitations: low accumulation levels of some recombinant proteins and lack of efficient purification methods. Elastin-like polypeptide (ELP), hydrophobin I (HFBI) and Zera® are three fusion partners found to increase the accumulation levels of recombinant proteins and induce the formation of protein bodies (PBs) in leaves when targeted to the endoplasmic reticulum (ER) in transient expression assays. In this study the effects of ELP and HFBI fusion tags on recombinant protein accumulation levels and PB formation was examined in stable transgenic Nicotiana tabacum.

RESULTS

The accumulation of recombinant protein and PB formation was evaluated in two cultivars of Nicotiana tabacum transformed with green fluorescent protein (GFP) fused to ELP or HFBI, both targeted and retrieved to the ER. The ELP and HFBI tags increased the accumulation of the recombinant protein and induced the formation of PBs in leaves of stable transgenic plants from both cultivars. Furthermore, these tags induced the formation of PBs in a concentration-dependent manner, where a specific level of recombinant protein accumulation was required for PBs to appear. Moreover, agro-infiltration of plants accumulating low levels of recombinant protein with p19, a suppressor of post-transcriptional gene silencing (PTGS), increased accumulation levels in four independent transgenic lines, suggesting that PTGS might have caused the low accumulation levels in these plants.

CONCLUSION

The use of ELP and HFBI tags as fusion partners in stable transgenic plants of tobacco is feasible and promising. In a constitutive environment, these tags increase the accumulation levels of the recombinant protein and induce the formation of PBs regardless of the cultivar used. However, a specific level of recombinant protein accumulation needs to be reached for PBs to form.


DOI: 10.1186/1472-6750-13-40
PubMed: 23663656
PubMed Central: PMC3659085


Affiliations:

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Le document en format XML

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<term>Elastin (metabolism)</term>
<term>Endoplasmic Reticulum (chemistry)</term>
<term>Endoplasmic Reticulum (metabolism)</term>
<term>Fungal Proteins (biosynthesis)</term>
<term>Fungal Proteins (genetics)</term>
<term>Fungal Proteins (metabolism)</term>
<term>Green Fluorescent Proteins (analysis)</term>
<term>Green Fluorescent Proteins (biosynthesis)</term>
<term>Green Fluorescent Proteins (genetics)</term>
<term>Green Fluorescent Proteins (metabolism)</term>
<term>Plant Leaves (chemistry)</term>
<term>Plant Leaves (metabolism)</term>
<term>Plants, Genetically Modified (genetics)</term>
<term>Plants, Genetically Modified (metabolism)</term>
<term>Protein Engineering (MeSH)</term>
<term>RNA Interference (MeSH)</term>
<term>Recombinant Fusion Proteins (analysis)</term>
<term>Recombinant Fusion Proteins (biosynthesis)</term>
<term>Recombinant Fusion Proteins (genetics)</term>
<term>Recombinant Fusion Proteins (metabolism)</term>
<term>Tobacco (genetics)</term>
<term>Tobacco (metabolism)</term>
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<term>Feuilles de plante (composition chimique)</term>
<term>Feuilles de plante (métabolisme)</term>
<term>Ingénierie des protéines (MeSH)</term>
<term>Interférence par ARN (MeSH)</term>
<term>Protéines de fusion recombinantes (analyse)</term>
<term>Protéines de fusion recombinantes (biosynthèse)</term>
<term>Protéines de fusion recombinantes (génétique)</term>
<term>Protéines de fusion recombinantes (métabolisme)</term>
<term>Protéines fongiques (biosynthèse)</term>
<term>Protéines fongiques (génétique)</term>
<term>Protéines fongiques (métabolisme)</term>
<term>Protéines à fluorescence verte (analyse)</term>
<term>Protéines à fluorescence verte (biosynthèse)</term>
<term>Protéines à fluorescence verte (génétique)</term>
<term>Protéines à fluorescence verte (métabolisme)</term>
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<term>Réticulum endoplasmique (métabolisme)</term>
<term>Tabac (génétique)</term>
<term>Tabac (métabolisme)</term>
<term>Végétaux génétiquement modifiés (génétique)</term>
<term>Végétaux génétiquement modifiés (métabolisme)</term>
<term>Élastine (biosynthèse)</term>
<term>Élastine (génétique)</term>
<term>Élastine (métabolisme)</term>
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<term>Recombinant Fusion Proteins</term>
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<term>Fungal Proteins</term>
<term>Green Fluorescent Proteins</term>
<term>Recombinant Fusion Proteins</term>
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<term>Fungal Proteins</term>
<term>Green Fluorescent Proteins</term>
<term>Recombinant Fusion Proteins</term>
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<term>Fungal Proteins</term>
<term>Green Fluorescent Proteins</term>
<term>Recombinant Fusion Proteins</term>
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<term>Protéines à fluorescence verte</term>
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<term>Plant Leaves</term>
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<term>Feuilles de plante</term>
<term>Réticulum endoplasmique</term>
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<term>Plants, Genetically Modified</term>
<term>Tobacco</term>
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<term>Protéines de fusion recombinantes</term>
<term>Protéines fongiques</term>
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<term>Tobacco</term>
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<term>Protéines de fusion recombinantes</term>
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<term>Protéines à fluorescence verte</term>
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<term>Végétaux génétiquement modifiés</term>
<term>Élastine</term>
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<term>RNA Interference</term>
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<b>BACKGROUND</b>
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<p>Plants are recognized as an efficient and inexpensive system to produce valuable recombinant proteins. Two different strategies have been commonly used for the expression of recombinant proteins in plants: transient expression mediated by Agrobacterium; or stable transformation of the plant genome. However, the use of plants as bioreactors still faces two main limitations: low accumulation levels of some recombinant proteins and lack of efficient purification methods. Elastin-like polypeptide (ELP), hydrophobin I (HFBI) and Zera® are three fusion partners found to increase the accumulation levels of recombinant proteins and induce the formation of protein bodies (PBs) in leaves when targeted to the endoplasmic reticulum (ER) in transient expression assays. In this study the effects of ELP and HFBI fusion tags on recombinant protein accumulation levels and PB formation was examined in stable transgenic Nicotiana tabacum.</p>
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<p>
<b>RESULTS</b>
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<p>The accumulation of recombinant protein and PB formation was evaluated in two cultivars of Nicotiana tabacum transformed with green fluorescent protein (GFP) fused to ELP or HFBI, both targeted and retrieved to the ER. The ELP and HFBI tags increased the accumulation of the recombinant protein and induced the formation of PBs in leaves of stable transgenic plants from both cultivars. Furthermore, these tags induced the formation of PBs in a concentration-dependent manner, where a specific level of recombinant protein accumulation was required for PBs to appear. Moreover, agro-infiltration of plants accumulating low levels of recombinant protein with p19, a suppressor of post-transcriptional gene silencing (PTGS), increased accumulation levels in four independent transgenic lines, suggesting that PTGS might have caused the low accumulation levels in these plants.</p>
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<b>CONCLUSION</b>
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<p>The use of ELP and HFBI tags as fusion partners in stable transgenic plants of tobacco is feasible and promising. In a constitutive environment, these tags increase the accumulation levels of the recombinant protein and induce the formation of PBs regardless of the cultivar used. However, a specific level of recombinant protein accumulation needs to be reached for PBs to form.</p>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Plants are recognized as an efficient and inexpensive system to produce valuable recombinant proteins. Two different strategies have been commonly used for the expression of recombinant proteins in plants: transient expression mediated by Agrobacterium; or stable transformation of the plant genome. However, the use of plants as bioreactors still faces two main limitations: low accumulation levels of some recombinant proteins and lack of efficient purification methods. Elastin-like polypeptide (ELP), hydrophobin I (HFBI) and Zera® are three fusion partners found to increase the accumulation levels of recombinant proteins and induce the formation of protein bodies (PBs) in leaves when targeted to the endoplasmic reticulum (ER) in transient expression assays. In this study the effects of ELP and HFBI fusion tags on recombinant protein accumulation levels and PB formation was examined in stable transgenic Nicotiana tabacum.</AbstractText>
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