2022
DOI: 10.3390/d14100861
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Genome-Wide Characterization and Identification of the YABBY Gene Family in Mango (Mangifera indica)

Abstract: YABBY is a specific transcription factor gene family in plants. It has the typical N-terminal C2C2-type zinc-finger domain and the C-terminal YABBY conservative structure domain, which play an important role in the development of the leaves and floral organs. The YABBY gene family directs leaf polarity in mango, playing an important role in maintaining species specificity. In this study, a total of seven YABBY genes were identified in the mango (Mangifera indica) genome. The seven YABBY family members possesse… Show more

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Cited by 3 publications
(7 citation statements)
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“…MdYABBY genes within the same clade had similar motif compositions. Similar results have been identified in A. thaliana [ 3 ], A. carambola [ 4 ], L. sativa [ 6 ], M. indica [ 22 ], Juglans regia and J. mandshurica [ 24 ], indicating that the YABBY gene family is highly conserved in plant.…”
Section: Discussionsupporting
confidence: 80%
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“…MdYABBY genes within the same clade had similar motif compositions. Similar results have been identified in A. thaliana [ 3 ], A. carambola [ 4 ], L. sativa [ 6 ], M. indica [ 22 ], Juglans regia and J. mandshurica [ 24 ], indicating that the YABBY gene family is highly conserved in plant.…”
Section: Discussionsupporting
confidence: 80%
“…This phenomenon is also found in L. sativa , which loses clade YABBY2 [ 6 ]. M. indica only has three clades, including CRC, YAB5, and YAB3 [ 22 ]. In addition, only four clades (CRC/DL, FIL, INO, and YAB2) were found in rice [ 11 ].…”
Section: Discussionmentioning
confidence: 99%
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“…In mango, X. campestris pv. mangiferaeindicae and C. gloeosporioides are the most representative bacterium and pathogenic fungus of mango, respectively [ 52 ]. We analyzed the MiCOMT genes’ expression levels during infection of the leaves with X. campestris pv.…”
Section: Discussionmentioning
confidence: 99%
“…We ground the plant material into a powder in liquid nitrogen and extracted it using an RNA extraction kit (centrifugal column type) (TIANGEN, Beijing, China) [83]. We used QuantStudio 6 Flex (Applied Biosystems, Waltham, MA, USA) to determine the expression of the gene and 2 −∆∆CT to calculate it [52,73]. The qRT-PCR primers of the MiCOMT genes were designed via Primer3 Plus (https://www.bioinformatics.nl/cgi%E2%80%93 bin/primer3 plus/primer3 plus.cgi, accessed on 14 March 2023) to determine the specific primers (Table S10) [84].…”
Section: Rna Isolation and Quantitative Real-time Pcr (Qrt-pcr)mentioning
confidence: 99%