TY - JOUR
T1 - Differential gene expression during floral transition in pineapple
AU - Paull, Robert E.
AU - Ksouri, Najla
AU - Kantar, Michael
AU - Zerpa-Catanho, Dessireé
AU - Chen, Nancy Jung
AU - Uruu, Gail
AU - Yue, Jingjing
AU - Guo, Shiyong
AU - Zheng, Yun
AU - Wai, Ching Man Jennifer
AU - Ming, Ray
N1 - The authors greatly appreciate the help provided by Liang Yu and Julie Nguyen in sequence library preparation and Kathleen Vickers for her help with editing. Dr. Paull was supported in part by the US Department of Agriculture, National Institute of Food and Agriculture, under an agreement 58‐2040‐5‐010 through the Agriculture Research Service and Hatch Project H862. The project would not be possible without the generous collaboration by Dole Food Company Hawaii who gave us access to their field for this research.
The authors greatly appreciate the help provided by Liang Yu and Julie Nguyen in sequence library preparation and Kathleen Vickers for her help with editing. Dr. Paull was supported in part by the US Department of Agriculture, National Institute of Food and Agriculture, under an agreement 58-2040-5-010 through the Agriculture Research Service and Hatch Project H862. The project would not be possible without the generous collaboration by Dole Food Company Hawaii who gave us access to their field for this research.
PY - 2023/11
Y1 - 2023/11
N2 - Pineapple (Ananas comosus var. comosus) and ornamental bromeliads are commercially induced to flower by treatment with ethylene or its analogs. The apex is transformed from a vegetative to a floral meristem and shows morphological changes in 8 to 10 days, with flowers developing 8 to 10 weeks later. During eight sampling stages ranging from 6 h to 8 days after treatment, 7961 genes were found to exhibit differential expression (DE) after the application of ethylene. In the first 3 days after treatment, there was little change in ethylene synthesis or in the early stages of the ethylene response. Subsequently, three ethylene response transcription factors (ERTF) were up-regulated and the potential gene targets were predicted to be the positive flowering regulator CONSTANS-like 3 (CO), a WUSCHEL gene, two APETALA1/FRUITFULL (AP1/FUL) genes, an epidermal patterning gene, and a jasmonic acid synthesis gene. We confirm that pineapple has lost the flowering repressor FLOWERING LOCUS C. At the initial stages, the SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1) was not significantly involved in this transition. Another WUSCHEL gene and a PHD homeobox transcription factor, though not apparent direct targets of ERTF, were up-regulated within a day of treatment, their predicted targets being the up-regulated CO, auxin response factors, SQUAMOSA, and histone H3 genes with suppression of abscisic acid response genes. The FLOWERING LOCUS T (FT), TERMINAL FLOWER (TFL), AGAMOUS-like APETELAR (AP2), and SEPETALA (SEP) increased rapidly within 2 to 3 days after ethylene treatment. Two FT genes were up-regulated at the apex and not at the leaf bases after treatment, suggesting that transport did not occur. These results indicated that the ethylene response in pineapple and possibly most bromeliads act directly to promote the vegetative to flower transition via APETALA1/FRUITFULL (AP1/FUL) and its interaction with SPL, FT, TFL, SEP, and AP2. A model based on AP2/ERTF DE and predicted DE target genes was developed to give focus to future research. The identified candidate genes are potential targets for genetic manipulation to determine their molecular role in flower transition.
AB - Pineapple (Ananas comosus var. comosus) and ornamental bromeliads are commercially induced to flower by treatment with ethylene or its analogs. The apex is transformed from a vegetative to a floral meristem and shows morphological changes in 8 to 10 days, with flowers developing 8 to 10 weeks later. During eight sampling stages ranging from 6 h to 8 days after treatment, 7961 genes were found to exhibit differential expression (DE) after the application of ethylene. In the first 3 days after treatment, there was little change in ethylene synthesis or in the early stages of the ethylene response. Subsequently, three ethylene response transcription factors (ERTF) were up-regulated and the potential gene targets were predicted to be the positive flowering regulator CONSTANS-like 3 (CO), a WUSCHEL gene, two APETALA1/FRUITFULL (AP1/FUL) genes, an epidermal patterning gene, and a jasmonic acid synthesis gene. We confirm that pineapple has lost the flowering repressor FLOWERING LOCUS C. At the initial stages, the SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1) was not significantly involved in this transition. Another WUSCHEL gene and a PHD homeobox transcription factor, though not apparent direct targets of ERTF, were up-regulated within a day of treatment, their predicted targets being the up-regulated CO, auxin response factors, SQUAMOSA, and histone H3 genes with suppression of abscisic acid response genes. The FLOWERING LOCUS T (FT), TERMINAL FLOWER (TFL), AGAMOUS-like APETELAR (AP2), and SEPETALA (SEP) increased rapidly within 2 to 3 days after ethylene treatment. Two FT genes were up-regulated at the apex and not at the leaf bases after treatment, suggesting that transport did not occur. These results indicated that the ethylene response in pineapple and possibly most bromeliads act directly to promote the vegetative to flower transition via APETALA1/FRUITFULL (AP1/FUL) and its interaction with SPL, FT, TFL, SEP, and AP2. A model based on AP2/ERTF DE and predicted DE target genes was developed to give focus to future research. The identified candidate genes are potential targets for genetic manipulation to determine their molecular role in flower transition.
KW - AGAMOUS
KW - APETALA1/FRUITFULL (AP1/FUL)
KW - Flowering Locus T
KW - Trans-Cis motifs
KW - ethylene response transcription factors
KW - floral transition
KW - flower regulators
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UR - http://www.scopus.com/inward/citedby.url?scp=85176396337&partnerID=8YFLogxK
U2 - 10.1002/pld3.541
DO - 10.1002/pld3.541
M3 - Article
C2 - 38028646
AN - SCOPUS:85176396337
SN - 2475-4455
VL - 7
JO - Plant Direct
JF - Plant Direct
IS - 11
M1 - e541
ER -