Literature DB >> 28032251

Long-term T-DNA insert stability and transgene expression consistency in field propagated sugarcane.

Kerry Hosmer Caffall1, Chengkun He2, Michele Smith-Jones3, Kristin Mayo1, Pearl Mai1, Shujie Dong1, John Ke1, Erik Dunder1, Michele Yarnall1, Rachel Whinna1, Joe DeMaio1, Weining Gu1, Judith Sheldon4, Martin Allen1, Tricia Costello1, Kristin Setliff1, Rakesh Jain5, Ada Snyder5, Clark Lovelady5, Eric Rawls5, Eric Palmer5, Yan Zhang1, Nicholas Bate1, Liang Shi1, Ian Jepson1.   

Abstract

KEY MESSAGE: This study addresses T-DNA insert stability and transgene expression consistency in multiple cycles of field propagated sugarcane. T-DNA inserts are stable; no transgene rearrangements were observed. AmCYAN1 and PMI protein accumulation levels were maintained. There was no evidence that production of either protein declined across generations and no transgene silencing was observed in three commercial sugarcane varieties through commercially relevant ratooning, propagation-by-setts, and micro-propagation generation processes over 4 years of field testing. Long term transgene expression consistency and T-DNA insert stability can be achieved in sugarcane, suggesting that it is highly probable that transgenic sugarcane can be successfully commercialized. This study addresses T-DNA insert stability and transgene expression consistency in multiple cycles of field propagated sugarcane. These data are critical supporting information needed for successful commercialization of GM sugarcane. Here seventeen transgenic events, containing the AmCYAN1 gene driven by a CMP promoter and the E. coli PMI gene driven by either a CMP or Ubi promoter, were used to monitor T-DNA insert stability and consistency of transgene encoded protein accumulation through commercially relevant ratooning, propagation-by-setts, and micro-propagation generation processes. The experiments were conducted in three commercial sugarcane varieties over 4 years of field testing. DNA gel blot analysis showed that the T-DNA inserts are stable; no transgene rearrangements were observed. Quantitative ELISA showed no evidence of decreasing AmCYAN1 and PMI protein levels across generations and no transgene silencing was observed. These results indicate that long term transgene expression consistency and T-DNA insert stability can be achieved in sugarcane, suggesting that it is highly probable that transgenic sugarcane can be successfully commercialized.

Entities:  

Keywords:  AmCYAN1; Expression consistency; PMI; T-DNA insert stability; Transgenic sugarcane

Mesh:

Substances:

Year:  2016        PMID: 28032251     DOI: 10.1007/s11103-016-0572-6

Source DB:  PubMed          Journal:  Plant Mol Biol        ISSN: 0167-4412            Impact factor:   4.076


  14 in total

1.  Posttranscriptional gene silencing in transgenic sugarcane. Dissection Of homology-dependent virus resistance in a monocot that has a complex polyploid genome

Authors: 
Journal:  Plant Physiol       Date:  1999-04       Impact factor: 8.340

2.  Quantitative real-time PCR assay for determining transgene copy number in transformed plants.

Authors:  D J Ingham; S Beer; S Money; G Hansen
Journal:  Biotechniques       Date:  2001-07       Impact factor: 1.993

3.  Comparative expression analysis of two sugarcane polyubiquitin promoters and flanking sequences in transgenic plants.

Authors:  Hairong Wei; Ming-Li Wang; Paul H Moore; Henrik H Albert
Journal:  J Plant Physiol       Date:  2003-10       Impact factor: 3.549

4.  Field performance of transgenic sugarcane produced using Agrobacterium and biolistics methods.

Authors:  Priya Joyce; Scott Hermann; Anthony O'Connell; Quang Dinh; Leonard Shumbe; Prakash Lakshmanan
Journal:  Plant Biotechnol J       Date:  2013-12-12       Impact factor: 9.803

5.  Recombinant cellulase accumulation in the leaves of mature, vegetatively propagated transgenic sugarcane.

Authors:  Mark D Harrison; R Jason Geijskes; Robyn Lloyd; Stacy Miles; Anthony Palupe; Manuel B Sainz; James L Dale
Journal:  Mol Biotechnol       Date:  2014-09       Impact factor: 2.695

6.  Ubiquitin promoter-based vectors for high-level expression of selectable and/or screenable marker genes in monocotyledonous plants.

Authors:  A H Christensen; P H Quail
Journal:  Transgenic Res       Date:  1996-05       Impact factor: 2.788

7.  Cestrum yellow leaf curling virus (CmYLCV) promoter: a new strong constitutive promoter for heterologous gene expression in a wide variety of crops.

Authors:  Livia Stavolone; Maria Kononova; Sandra Pauli; Antonio Ragozzino; Peter de Haan; Steve Milligan; Kay Lawton; Thomas Hohn
Journal:  Plant Mol Biol       Date:  2003-11       Impact factor: 4.076

8.  Efficient silencing of reporter transgenes coupled to known functional promoters in sugarcane, a highly polyploid crop species.

Authors:  Stephen R Mudge; Kenji Osabe; Rosanne E Casu; Graham D Bonnett; John M Manners; Robert G Birch
Journal:  Planta       Date:  2008-11-15       Impact factor: 4.116

9.  Transgenic rice plants harboring an introduced potato proteinase inhibitor II gene are insect resistant.

Authors:  X Duan; X Li; Q Xue; M Abo-el-Saad; D Xu; R Wu
Journal:  Nat Biotechnol       Date:  1996-04       Impact factor: 54.908

10.  Transgenic maize plants expressing a fungal phytase gene.

Authors:  Rumei Chen; Guangxing Xue; Ping Chen; Bin Yao; Wenzhu Yang; Qianli Ma; Yunliu Fan; Zuoyu Zhao; Mitchell C Tarczynski; Jinrui Shi
Journal:  Transgenic Res       Date:  2007-10-12       Impact factor: 2.788

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  1 in total

Review 1.  Phytohormone signalling and cross-talk to alleviate aluminium toxicity in plants.

Authors:  Alok Ranjan; Ragini Sinha; Shambhu Krishan Lal; Sujit Kumar Bishi; Anil Kumar Singh
Journal:  Plant Cell Rep       Date:  2021-06-04       Impact factor: 4.570

  1 in total

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