2015
DOI: 10.1016/j.plantsci.2014.11.004
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Ectopic expression of a Catalpa bungei (Bignoniaceae) PISTILLATA homologue rescues the petal and stamen identities in Arabidopsis pi-1 mutant

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Cited by 30 publications
(43 citation statements)
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“…Our results, therefore, revealed that LFMADS2 may have the activity of B-class MADS-box transcription factor because the ectopic expression in Arabidopsis ( PI/pi background) turned the sepals into petaloid organs, although restoration of petals and stamens formation was not observed in this heterozygote pi-1 mutant with the overexpressed LFMADS2. This notion also has been observed in previous studies on PI homologue of other plant species, in which ectopic overexpression of other B-class MADS-box genes CabuPI led to the petaloid sepals change in transgenic Arabidopsis with PI / pi background [68]. …”
Section: Resultssupporting
confidence: 78%
“…Our results, therefore, revealed that LFMADS2 may have the activity of B-class MADS-box transcription factor because the ectopic expression in Arabidopsis ( PI/pi background) turned the sepals into petaloid organs, although restoration of petals and stamens formation was not observed in this heterozygote pi-1 mutant with the overexpressed LFMADS2. This notion also has been observed in previous studies on PI homologue of other plant species, in which ectopic overexpression of other B-class MADS-box genes CabuPI led to the petaloid sepals change in transgenic Arabidopsis with PI / pi background [68]. …”
Section: Resultssupporting
confidence: 78%
“…Amino acid sequences of these proteins, which contain the M, I, K, and C domains, were aligned using a ClustalW program (Thompson et al, 1994). A phylogenetic tree was constructed using MEGA 5.0 software (Kumar et al, 2008;Tamura et al, 2011) and the method described by Jing et al (2015). Parameters of the phylogenetic tree were the bootstrap of 1,000 replicates, substitution model of Jones-Taylor-Thornton (Jones et al, 1992), uniform rates, nearest neighbor interchange, and the complete deletion of gaps/missing data.…”
Section: Sequence Alignments and Phylogenetic Analysismentioning
confidence: 99%
“…The qRT-PCR were assayed using the SYBR green I (Takara, Japan) and CFX96 Touch Real-time PCR Detection System (Bio-Rad, USA). The reaction mixture was cycled using the previous parameters described by Jing et al (2015). As an internal control, the E. japonica b-actin was used to normalize small differences in template amounts with the primers qEjactinF and qEjactinR (Shan et al, 2008).…”
Section: Sequence Alignments and Phylogenetic Analysismentioning
confidence: 99%
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