Generation of a selectable marker free, highly expressed single copy locus as landing pad for transgene stacking in sugarcane

Authors
Zhao, YangKim, Jae Y.Karan, RatnaJung, Je H.Pathak, BhuvanWilliamson, BruceKannan, BaskaranWang, DuoduoFan, ChunyangYu, WenjinDong, ShujieSrivastava, VibhaAltpeter, Fredy
Issue Date
2019-06
Publisher
SPRINGER
Citation
PLANT MOLECULAR BIOLOGY, v.100, no.3, pp.247 - 263
Abstract
Sugarcane, a tropical C4 grass in the genus Saccharum (Poaceae), accounts for nearly 80% of sugar produced worldwide and is also an important feedstock for biofuel production. Generating transgenic sugarcane with predictable and stable transgene expression is critical for crop improvement. In this study, we generated a highly expressed single copy locus as landing pad for transgene stacking. Transgenic sugarcane lines with stable integration of a single copy nptII expression cassette flanked by insulators supported higher transgene expression along with reduced line to line variation when compared to single copy events without insulators by NPTII ELISA analysis. Subsequently, the nptII selectable marker gene was efficiently excised from the sugarcane genome by the FLPe/FRT site-specific recombination system to create selectable marker free plants. This study provides valuable resources for future gene stacking using site-specific recombination or genome editing tools.
Keywords
SITE-SPECIFIC RECOMBINATION; VECTOR BACKBONE SEQUENCES; T-DNA; PARTICLE BOMBARDMENT; GENE INTEGRATION; CHALCONE SYNTHASE; RICE PLANTS; AGROBACTERIUM; TRANSFORMATION; ARABIDOPSIS; Sugarcane; Selection marker removal; Site-specific recombination; Insulator; FLP; FLPe
ISSN
0167-4412
URI
https://pubs.kist.re.kr/handle/201004/119917
DOI
10.1007/s11103-019-00856-4
Appears in Collections:
KIST Article > 2019
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE