2016
DOI: 10.1007/s11240-016-0992-7
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Regeneration selection improves transformation efficiency in narrow-leaf lupin

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Cited by 14 publications
(9 citation statements)
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“…This study provided novel evidences supporting the concept that RAP2.7 may control low-alkaloid iucundus phenotype, however, further evidence would require cis -trans tests. Nonetheless, such studies are hampered by very low transformation efficiency in narrow-leafed lupin [70].…”
Section: Resultsmentioning
confidence: 99%
“…This study provided novel evidences supporting the concept that RAP2.7 may control low-alkaloid iucundus phenotype, however, further evidence would require cis -trans tests. Nonetheless, such studies are hampered by very low transformation efficiency in narrow-leafed lupin [70].…”
Section: Resultsmentioning
confidence: 99%
“…In such a scenario, deletion of two copies of the BES1 binding site motif via the 1,208‐bp INDEL genotype would be sufficient to elevate LanFTc1 expression to an intermediate level, and deletion of all three motifs via the 1,423‐ or 5,162‐bp INDELs would fully derepress expression. With genome editing tools, such as the CRISPR/Cas‐9 system (Bortesi & Fischer, ), and more efficient transformation protocols in narrow‐leafed lupin (Barker et al, ), it may be feasible to modify BES1 binding site motifs in the wild‐type sequence to test the validity of this hypothesis in the future. If BES1 has a role in regulating LanFTc1 , BES1's known involvement within the photoperiodic pathway could explain why cultivars with the 1,423‐bp deletion are also less responsive to inductive long days than wild‐types without the large deletion in the promoter region of LanFTc1 (J. D. Berger, unpublished data).…”
Section: Discussionmentioning
confidence: 99%
“…As has been demonstrated in Arabidopsis, increasing from three to four tandem repeats of a 7-bp motif for CYCLING DOF FACTOR 1 in the promoter of CO increases the day-time repression of this gene and significantly delays flowering time (Rosas et al, 2014). We identified motifs for the binding site of a single transcription factor, named BES1, present once within the C H and twice within the C M critical regions (Tables 2, S4, and S5), yet nowhere else in the 5' UTR and 5' regulatory region of (Bortesi & Fischer, 2015), and more efficient transformation protocols in narrow-leafed lupin (Barker et al, 2016), it may be feasible to modify BES1 binding site motifs in the wild-type sequence to test the validity of this hypothesis in the future. If BES1 has a role in regulating LanFTc1, BES1's known involvement within the photoperiodic pathway could explain why cultivars with the 1,423-bp deletion are also less responsive to inductive long days than wild-types without the large deletion in the promoter region of LanFTc1 (J. D. Berger, unpublished data).…”
Section: Assessment Of Linkage Disequilibrium In the Lanftc1 Genomimentioning
confidence: 97%
“…The function of candidate genes may be studied by genetic transformation of lupin, the primary method being Agrobacterium tumefaciens -mediated transformation of wounded seedling shoot apical meristems to generate transgenic shoots ( Pigeaire et al, 1997 ). While transformation efficiencies are low due to low survival and chimeric nature of T 0 plants, this method has been successful in generating transgenic NLL ( Molvig et al, 1997 ; Pigeaire et al, 1997 ; Wijayanto et al, 2009 ; Tabe et al, 2010 ; Atkins et al, 2011 ; Barker et al, 2016 ), L. luteus ( Li et al, 2000 ; Pniewski et al, 2006 ), and L. mutabilis ( Babaoglu et al, 2000 ; Polowick et al, 2014 ) to confer various traits, with recent modifications improving this transformation method for NLL ( Nguyen et al, 2016a , b ). For L. albus , however, A. tumefaciens -mediated transformation has been unsuccessful and as such hairy root transformation using A. rhizogenes ( Uhde-Stone et al, 2005 ; Sbabou et al, 2010 ; Cheng et al, 2011 ) and VIGS using the Peanut stunt virus vector ( Yamagishi et al, 2015 ) have been used to study gene function in this species.…”
Section: Future Prospectsmentioning
confidence: 99%