2022
DOI: 10.1016/j.jare.2021.12.004
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Multi-omics analysis reveals the genetic basis of rice fragrance mediated by betaine aldehyde dehydrogenase 2

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Cited by 14 publications
(13 citation statements)
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“…The badh2-E2 allele carried by ‘Changxianggeng 1813’ was consistent with that in a number of Chinese fragrant japonica rice cultivars, e.g., ‘Wuxiang 9915’, ‘Xiangjing 111’, ‘Zhenxiangjing 5’, suggesting that this allele is common by descent in Chinese fragrant rice cultivars [ 8 , 13 ]. Phylogenetic analysis of BADH2 haplotype data ( Figure S1b ) further showed that the badh2-E2 allele in ‘Changxianggeng 1813’ clustered together with a previously identified haplotype sequence endemic to two cultivated japonica rice (see [ 2 ] for full details). Taken together, these findings provided additional support for the previous studies indicating that badh2-E2 may arise and become fixed in the japonica gene pool [ 7 , 8 , 13 ].…”
Section: Resultsmentioning
confidence: 61%
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“…The badh2-E2 allele carried by ‘Changxianggeng 1813’ was consistent with that in a number of Chinese fragrant japonica rice cultivars, e.g., ‘Wuxiang 9915’, ‘Xiangjing 111’, ‘Zhenxiangjing 5’, suggesting that this allele is common by descent in Chinese fragrant rice cultivars [ 8 , 13 ]. Phylogenetic analysis of BADH2 haplotype data ( Figure S1b ) further showed that the badh2-E2 allele in ‘Changxianggeng 1813’ clustered together with a previously identified haplotype sequence endemic to two cultivated japonica rice (see [ 2 ] for full details). Taken together, these findings provided additional support for the previous studies indicating that badh2-E2 may arise and become fixed in the japonica gene pool [ 7 , 8 , 13 ].…”
Section: Resultsmentioning
confidence: 61%
“…The BADH2 gene sequence for ‘Changxianggeng 1813’ was extracted from its genome sequence according to annotation files and then compared to that of the non-fragrant cultivar Nipponbare using the MAFFT multiple sequence alignment program [ 75 ], to verify the presence/absence of the mutations associated with fragrance in ‘Changxianggeng 1813’. The BADH2 protein-coding sequence for ‘Changxianggeng 1813’, was further combined with previously published 38 haplotypes in the BADH2 coding region for phylogenetic analysis [ 2 ]. All 39 BADH2 coding sequences were aligned using ClustalW [ 76 ], and the resulting alignment was used for Neighbor-Joining (NJ) phylogenetic tree construction using MEGA v.11.0.11 [ 77 ], with 1000 bootstrap replicates.…”
Section: Methodsmentioning
confidence: 99%
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“…We utilized different databases for designing the Axiom rice genotyping chip:1) Resequencing data of Korean World Rice Collection (KRICE) of 475 accessions composed of 417 cultivated and 58 wild accessions ( Phitaktansakul et al., 2021 ), 2) Rice genome project data of 3,000 accessions (3 K-RGP) from the International Rice Research Institute (IRRI) ( ), 3) High-Density Rice Array (HDRA, 700K) array reported from Cornell university ( McCouch et al., 2016 ), 4) Affymetrix 44 K Rice Chip (Affy44K) ( Zhao et al., 2011 ), 5) QTARO database ( ) ( Yonemaru et al., 2010 ), 6) Plant Reactome Gramene Pathways database ( ) 7) Chloroplast ( Tong et al., 2016 ; Cheng et al., 2019 ) and mitochondria ( Tong et al., 2017 ) genomic sequences of japonica and rufipogon and 8) GMO, we used transgenic plants and genomes of various microorganisms as references for GMO marker design. The known GMO events consisted of host and insert regions; we utilized NCBI Primer-BLAST tool to get the full-length products and modified them into Axiom probes for 155 events.…”
Section: Methodsmentioning
confidence: 99%