| Literature DB >> 27600536 |
Keith Lowe1, Emily Wu1, Ning Wang1, George Hoerster1, Craig Hastings1, Myeong-Je Cho2, Chris Scelonge1, Brian Lenderts1, Mark Chamberlin1, Josh Cushatt1, Lijuan Wang1, Larisa Ryan1, Tanveer Khan3, Julia Chow-Yiu1, Wei Hua1, Maryanne Yu2, Jenny Banh2, Zhongmeng Bao1, Kent Brink4, Elizabeth Igo4, Bhojaraja Rudrappa5, P M Shamseer5, Wes Bruce6, Lisa Newman1, Bo Shen1, Peizhong Zheng7, Dennis Bidney1, Carl Falco1, Jim Register1, Zuo-Yu Zhao1, Deping Xu1, Todd Jones1, William Gordon-Kamm8.
Abstract
While transformation of the major monocot crops is currently possible, the process typically remains confined to one or two genotypes per species, often with poor agronomics, and efficiencies that place these methods beyond the reach of most academic laboratories. Here, we report a transformation approach involving overexpression of the maize (Zea mays) Baby boom (Bbm) and maize Wuschel2 (Wus2) genes, which produced high transformation frequencies in numerous previously nontransformable maize inbred lines. For example, the Pioneer inbred PHH5G is recalcitrant to biolistic and Agrobacterium tumefaciens transformation. However, when Bbm and Wus2 were expressed, transgenic calli were recovered from over 40% of the starting explants, with most producing healthy, fertile plants. Another limitation for many monocots is the intensive labor and greenhouse space required to supply immature embryos for transformation. This problem could be alleviated using alternative target tissues that could be supplied consistently with automated preparation. As a major step toward this objective, we transformed Bbm and Wus2 directly into either embryo slices from mature seed or leaf segments from seedlings in a variety of Pioneer inbred lines, routinely recovering healthy, fertile T0 plants. Finally, we demonstrated that the maize Bbm and Wus2 genes stimulate transformation in sorghum (Sorghum bicolor) immature embryos, sugarcane (Saccharum officinarum) callus, and indica rice (Oryza sativa ssp indica) callus.Entities:
Year: 2016 PMID: 27600536 PMCID: PMC5059793 DOI: 10.1105/tpc.16.00124
Source DB: PubMed Journal: Plant Cell ISSN: 1040-4651 Impact factor: 11.277