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Journal articles on the topic 'APETALA2'

Author: Grafiati

Published: 31 August 2024

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1

Liu, Z., and E. M. Meyerowitz. "LEUNIG regulates AGAMOUS expression in Arabidopsis flowers." Development 121, no. 4 (1995): 975–91. http://dx.doi.org/10.1242/dev.121.4.975.

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LEUNIG was identified in a genetic screen designed to isolate second-site enhancer mutations of the floral homeotic mutant apetala2-1. leunig mutations not only enhance apetala2, but by themselves cause a similar but less-pronounced homeotic transformation than apetala2 mutations. leunig flowers have sepals that are transformed toward stamens and carpels, and petals that are either staminoid or absent. In situ hybridization experiments with leunig mutants revealed altered expression pattern of the floral homeotic genes APETALA1, APETALA3, PISTILLATA, and AGAMOUS. Double mutants of leunig and a

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2

Schultz, E. A., and G. W. Haughn. "Genetic analysis of the floral initiation process (FLIP) in Arabidopsis." Development 119, no. 3 (1993): 745–65. http://dx.doi.org/10.1242/dev.119.3.745.

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Within the Arabidopsis inflorescence, two distinct developmental phases exist. The early inflorescence phase is characterized by nodes bearing coflorescences and leaves, and the late inflorescence phase by nodes bearing flowers. Four genes, TERMINAL FLOWER 1, LEAFY, APETALA1 and APETALA2 are necessary to initiate the switch from formation of early to formation of late inflorescence nodes at the appropriate time. We have investigated the relative roles of these genes in development by isolating and characterizing new alleles of TERMINAL FLOWER 1, LEAFY and APETALA1, and by constructing double m

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3

Clark, S. E., M. P. Running, and E. M. Meyerowitz. "CLAVATA1, a regulator of meristem and flower development in Arabidopsis." Development 119, no. 2 (1993): 397–418. http://dx.doi.org/10.1242/dev.119.2.397.

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We have investigated the effects on plant development of mutations in the Arabidopsis thaliana CLAVATA1 gene. In clavata1 plants, vegetative, inflorescence and floral meristems are all enlarged relative to wild type. The apical meristem can fasciate in the more severe mutant alleles, and this fasciation can occur prior to the transition to flowering. Flowers of clavata1 plants can have increased numbers of organs in all four whorls, and can also have additional whorls not present in wild-type flowers. Double mutant combinations of clavata1 with agamous, apetala2, apetala3 and pistillata indica

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4

Bowman, J. L., J. Alvarez, D. Weigel, E. M. Meyerowitz, and D. R. Smyth. "Control of flower development in Arabidopsis thaliana by APETALA1 and interacting genes." Development 119, no. 3 (1993): 721–43. http://dx.doi.org/10.1242/dev.119.3.721.

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Mutations in the APETALA1 gene disturb two phases of flower development, flower meristem specification and floral organ specification. These effects become manifest as a partial conversion of flowers into inflorescence shoots and a disruption of sepal and petal development. We describe the changes in an allelic series of nine apetala1 mutants and show that the two functions of APETALA1 are separable. We have also studied the interaction between APETALA1 and other floral genes by examining the phenotypes of multiply mutant plants and by in situ hybridization using probes for several floral cont

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5

Bowman, J. L., D. R. Smyth, and E. M. Meyerowitz. "Genetic interactions among floral homeotic genes of Arabidopsis." Development 112, no. 1 (1991): 1–20. http://dx.doi.org/10.1242/dev.112.1.1.

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We describe allelic series for three loci, mutations in which result in homeotic conversions in two adjacent whorls in the Arabidopsis thaliana flower. Both the structure of the mature flower and its development from the initial primordium are described by scanning electron microscopy. New mutations at the APETALA2 locus, ap2-2, ap2-8 and ap2-9, cause homeotic conversions in the outer two whorls: sepals to carpels (or leaves) and petals to stamens. Two new mutations of PISTILLATA, pi-2 and pi-3, cause second and third whorl organs to differentiate incorrectly. Homeotic conversions are petals t

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6

H D D Bandupriya. "Expression of Aintegumenta-like Gene Related to Embryogenic Competence in Coconut Confirmed by 454-pyrosequencing Transcriptome Analysis." CORD 31, no. 2 (2015): 11. http://dx.doi.org/10.37833/cord.v31i2.58.

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A member of the Aintegumenta sub-family of Apetala gene family encoding two APETALA2 (AP2) domains was isolated and termed as Cocos nucifera Aintegumenta like gene (CnANT). The deduced amino acid sequence of the conserved domains shared a high similarity with Aintegumenta-Like (ANT like) genes in Arabidopsis thaliana, Elaeis guineensis, Oryza sativa. Comparison of transcriptomes in different tissues revealed that CnANT transcripts were high in mature zygotic embryo (12 months after pollination; 12ME). Quantitative RT-PCR results confirmed the higher CnANT transcript accumulation in mature zygo

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7

Okamuro, Jack K., Wayne Szeto, Cynthia Lotys-Prass, and K. Diane Jofuku. "Photo and Hormonal Control of Meristem Identity in the Arabidopsis Flower Mutants apetala2 and apetala1." Plant Cell 9, no. 1 (1997): 37. http://dx.doi.org/10.2307/3870369.

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8

Widiyanto, Srinanan M., Eri Mustari, Diky Setya Diningrat, and Rina Ratnasih. "APETALA2 and APETALA3 Genes Expression Profiling on Floral Development of Teak (Tectona grandis Linn f.)." Journal of Plant Sciences 11, no. 4 (2016): 61–68. http://dx.doi.org/10.3923/jps.2016.61.68.

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9

Okamuro, J. K., W. Szeto, C. Lotys-Prass, and K. D. Jofuku. "Photo and hormonal control of meristem identity in the Arabidopsis flower mutants apetala2 and apetala1." Plant Cell 9, no. 1 (1997): 37–47. http://dx.doi.org/10.1105/tpc.9.1.37.

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10

Bowman, J. L., H. Sakai, T. Jack, D. Weigel, U. Mayer, and E. M. Meyerowitz. "SUPERMAN, a regulator of floral homeotic genes in Arabidopsis." Development 114, no. 3 (1992): 599–615. http://dx.doi.org/10.1242/dev.114.3.599.

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We describe a locus, SUPERMAN, mutations in which result in extra stamens developing at the expense of the central carpels in the Arabidopsis thaliana flower. The development of superman flowers, from initial primordium to mature flower, is described by scanning electron microscopy. The development of doubly and triply mutant strains, constructed with superman alleles and previously identified homeotic mutations that cause alterations in floral organ identity, is also described. Essentially additive phenotypes are observed in superman agamous and superman apetala2 double mutants. The epistatic

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11

Patil, Vrushali, Hannah I. McDermott, Trisha McAllister, et al. "APETALA2 control of barley internode elongation." Development 146, no. 11 (2019): dev170373. http://dx.doi.org/10.1242/dev.170373.

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12

Ohto, M. a., R. L. Fischer, R. B. Goldberg, K. Nakamura, and J. J. Harada. "Control of seed mass by APETALA2." Proceedings of the National Academy of Sciences 102, no. 8 (2005): 3123–28. http://dx.doi.org/10.1073/pnas.0409858102.

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13

Lin, Wanping, Suresh Kumar Gupta, Tzahi Arazi, and Ben Spitzer-Rimon. "MIR172d Is Required for Floral Organ Identity and Number in Tomato." International Journal of Molecular Sciences 22, no. 9 (2021): 4659. http://dx.doi.org/10.3390/ijms22094659.

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MicroRNA172 (miR172) functions as a central regulator of flowering time and flower development by post-transcriptional repression of APETALA2-LIKE transcription factors. In the model crop Solanum lycopersicum (tomato), the miR172 family is still poorly annotated and information about the functions of specific members is lacking. Here, de-novo prediction of tomato miR172 coding loci identified seven genes (SlMIR172a-g), that code for four unique species of miR172 (sly-miR172). During reproductive development, sly-miR172s are differentially expressed, with sly-miR172c and sly-miR172d being the m

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14

Crone, Wilson, and Elizabeth M. Lord. "Floral organ initiation and development in wild-type Arabidopsis thaliana (Brassicaceae) and in the organ identity mutants apetala2-1 and agamous-1." Canadian Journal of Botany 72, no. 3 (1994): 384–401. http://dx.doi.org/10.1139/b94-052.

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The flowers of Arabidopsis thaliana (Brassicaceae) were examined for histological events during organ initiation and later development. An inflorescence floral plastochron of the main stem raceme was used as a basis for the timing and staging of developmental events. Sepals, petals, stamens, and carpels in wild-type Landsberg erecta Arabidopsis are distinguishable as primordia in terms of cell division events associated with initiation, size, and component cell numbers. Flower organogenesis in the organ identity (homeotic) mutants apetala2-1 and agamous-1 was compared with that of the wild typ

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15

Hill, T. A., C. D. Day, S. C. Zondlo, A. G. Thackeray, and V. F. Irish. "Discrete spatial and temporal cis-acting elements regulate transcription of the Arabidopsis floral homeotic gene APETALA3." Development 125, no. 9 (1998): 1711–21. http://dx.doi.org/10.1242/dev.125.9.1711.

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The APETALA3 floral homeotic gene is required for petal and stamen development in Arabidopsis. APETALA3 transcripts are first detected in a meristematic region that will give rise to the petal and stamen primordia, and expression is maintained in this region during subsequent development of these organs. To dissect how the APETALA3 gene is expressed in this spatially and temporally restricted domain, various APETALA3 promoter fragments were fused to the uidA reporter gene encoding beta-glucuronidase and assayed for the resulting patterns of expression in transgenic Arabidopsis plants. Based on

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16

Chandler, John W. "Class VIIIb APETALA2 Ethylene Response Factors in Plant Development." Trends in Plant Science 23, no. 2 (2018): 151–62. http://dx.doi.org/10.1016/j.tplants.2017.09.016.

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17

Bomblies, Kirsten, Nicole Dagenais, and Detlef Weigel. "Redundant Enhancers Mediate Transcriptional Repression of AGAMOUS by APETALA2." Developmental Biology 216, no. 1 (1999): 260–64. http://dx.doi.org/10.1006/dbio.1999.9504.

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18

Alegría-Mundo, H., L. Yong, A. Cruz-Ramírez, L. Herrera-Estrella, and A. Cruz-Hernández. "MOLECULAR ANALYSIS OF MARIGOLD (TAGETES ERECTA) APETALA2 IN FLOWER DEVELOPMENT." Acta Horticulturae, no. 929 (March 2012): 293–98. http://dx.doi.org/10.17660/actahortic.2012.929.43.

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19

Kim, Sangtae, Pamela S. Soltis, Kerr Wall, and Douglas E. Soltis. "Phylogeny and Domain Evolution in the APETALA2-like Gene Family." Molecular Biology and Evolution 23, no. 1 (2005): 107–20. http://dx.doi.org/10.1093/molbev/msj014.

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20

Ó’Maoiléidigh, Diarmuid S., Annabel D. van Driel, Anamika Singh, et al. "Systematic analyses of the MIR172 family members of Arabidopsis define their distinct roles in regulation of APETALA2 during floral transition." PLOS Biology 19, no. 2 (2021): e3001043. http://dx.doi.org/10.1371/journal.pbio.3001043.

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MicroRNAs (miRNAs) play important roles in regulating flowering and reproduction of angiosperms. Mature miRNAs are encoded by multipleMIRNAgenes that can differ in their spatiotemporal activities and their contributions to gene regulatory networks, but the functions of individualMIRNAgenes are poorly defined. We functionally analyzed the activity of all 5Arabidopsis thaliana MIR172genes, which encode miR172 and promote the floral transition by inhibiting the accumulation of APETALA2 (AP2) and APETALA2-LIKE (AP2-LIKE) transcription factors (TFs). Through genome editing and detailed confocal mic

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21

Xie, Xiu-lan, Xue-ren Yin, and Kun-song Chen. "Roles of APETALA2/Ethylene-Response Factors in Regulation of Fruit Quality." Critical Reviews in Plant Sciences 35, no. 2 (2016): 120–30. http://dx.doi.org/10.1080/07352689.2016.1213119.

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22

Würschum, Tobias, Rita Groß-Hardt, and Thomas Laux. "APETALA2 Regulates the Stem Cell Niche in the Arabidopsis Shoot Meristem." Plant Cell 18, no. 2 (2005): 295–307. http://dx.doi.org/10.1105/tpc.105.038398.

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23

Eckardt, Nancy A. "A Role for APETALA2 in Maintenance of the Stem Cell Niche." Plant Cell 18, no. 2 (2006): 275–77. http://dx.doi.org/10.1105/tpc.106.040972.

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24

Tang, Meifang, Guisheng Li, and Mingsheng Chen. "The Phylogeny and Expression Pattern of APETALA2-like Genes in Rice." Journal of Genetics and Genomics 34, no. 10 (2007): 930–38. http://dx.doi.org/10.1016/s1673-8527(07)60104-0.

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25

Liu, Zhaolei, Chunsun Gu, Fadi Chen, et al. "Identification and Expression of an APETALA2-Like Gene from Nelumbo nucifera." Applied Biochemistry and Biotechnology 168, no. 2 (2012): 383–91. http://dx.doi.org/10.1007/s12010-012-9782-9.

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26

Cheng, Cheng, Likun An, Fangzhe Li, et al. "Wide-Range Portrayal of AP2/ERF Transcription Factor Family in Maize (Zea mays L.) Development and Stress Responses." Genes 14, no. 1 (2023): 194. http://dx.doi.org/10.3390/genes14010194.

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The APETALA2/Ethylene-Responsive Transcriptional Factors containing conservative AP2/ERF domains constituted a plant-specific transcription factor (TF) superfamily, called AP2/ERF. The configuration of the AP2/ERF superfamily in maize has remained unresolved. In this study, we identified the 229 AP2/ERF genes in the latest (B73 RefGen_v5) maize reference genome. Phylogenetic classification of the ZmAP2/ERF family members categorized it into five clades, including 27 AP2 (APETALA2), 5 RAV (Related to ABI3/VP), 89 DREB (dehydration responsive element binding), 105 ERF (ethylene responsive factor

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27

Jofuku, K. Diane, Bart G. W. den Boer, Marc Van Montagu, and Jack K. Okamuro. "Control of Arabidopsis Flower and Seed Development by the Homeotic Gene APETALA2." Plant Cell 6, no. 9 (1994): 1211. http://dx.doi.org/10.2307/3869820.

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28

Finkelstein, Ruth R., Ming Li Wang, Tim J. Lynch, Shashirekha Rao, and Howard M. Goodman. "The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein." Plant Cell 10, no. 6 (1998): 1043. http://dx.doi.org/10.2307/3870689.

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29

Martínez-Fernández, Irene, Stéfanie Menezes de Moura, Marcio Alves-Ferreira, Cristina Ferrándiz, and Vicente Balanzà. "Identification of Players Controlling Meristem Arrest Downstream of the FRUITFULL-APETALA2 Pathway." Plant Physiology 184, no. 2 (2020): 945–59. http://dx.doi.org/10.1104/pp.20.00800.

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30

Chen, X. "A MicroRNA as a Translational Repressor of APETALA2 in Arabidopsis Flower Development." Science 303, no. 5666 (2004): 2022–25. http://dx.doi.org/10.1126/science.1088060.

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31

Finkelstein, Ruth R., Ming Li Wang, Tim J. Lynch, Shashirekha Rao, and Howard M. Goodman. "The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein." Plant Cell 10, no. 6 (1998): 1043–54. http://dx.doi.org/10.1105/tpc.10.6.1043.

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32

Jofuku, K. D., B. G. den Boer, M. Van Montagu, and J. K. Okamuro. "Control of Arabidopsis flower and seed development by the homeotic gene APETALA2." Plant Cell 6, no. 9 (1994): 1211–25. http://dx.doi.org/10.1105/tpc.6.9.1211.

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33

Vahala, Tiina, Bengt Oxelman, and Sara von Arnold. "Two APETALA2‐like genes of Picea abies are differentially expressed during development1." Journal of Experimental Botany 52, no. 358 (2001): 1111–15. http://dx.doi.org/10.1093/jexbot/52.358.1111.

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34

Chandler, J. W., and W. Werr. "A phylogenetically conserved APETALA2/ETHYLENE RESPONSE FACTOR, ERF12, regulates Arabidopsis floral development." Plant Molecular Biology 102, no. 1-2 (2019): 39–54. http://dx.doi.org/10.1007/s11103-019-00936-5.

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Abstract Key message Arabidopsis ETHYLENE RESPONSE FACTOR12 (ERF12), the rice MULTIFLORET SPIKELET1 orthologue pleiotropically affects meristem identity, floral phyllotaxy and organ initiation and is conserved among angiosperms. Abstract Reproductive development necessitates the coordinated regulation of meristem identity and maturation and lateral organ initiation via positive and negative regulators and network integrators. We have identified ETHYLENE RESPONSE FACTOR12 (ERF12) as the Arabidopsis orthologue of MULTIFLORET SPIKELET1 (MFS1) in rice. Loss of ERF12 function pleiotropically affect

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35

Drews, Gary N., John L. Bowman, and Elliot M. Meyerowitz. "Negative regulation of the Arabidopsis homeotic gene AGAMOUS by the APETALA2 product." Cell 65, no. 6 (1991): 991–1002. http://dx.doi.org/10.1016/0092-8674(91)90551-9.

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36

Gao, Jin, Yaoxin Zhang, Zhengguo Li, and Mingchun Liu. "Role of ethylene response factors (ERFs) in fruit ripening." Food Quality and Safety 4, no. 1 (2020): 15–20. http://dx.doi.org/10.1093/fqsafe/fyz042.

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Abstract The ethylene response factors (ERFs) belong to the APETALA2/ethylene response factor (AP2/ERF) superfamily and act downstream of the ethylene signalling pathway to regulate the expression of ethylene responsive genes. In different species, ERFs have been reported to be involved in plant development, flower abscission, fruit ripening, and defense responses. In this review, based on the new progress made by recent studies, we summarize the specific role and mode of action of ERFs in regulating different aspects of ripening in both climacteric and non-climacteric fruits, and provide new

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37

Weigel, Detlef. "The APETALA2 Domain Is Related to a Novel Type of DNA Binding Domain." Plant Cell 7, no. 4 (1995): 388. http://dx.doi.org/10.2307/3870077.

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38

Moose, S. P., and P. H. Sisco. "Glossy15, an APETALA2-like gene from maize that regulates leaf epidermal cell identity." Genes & Development 10, no. 23 (1996): 3018–27. http://dx.doi.org/10.1101/gad.10.23.3018.

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39

Jofuku, K. D., P. K. Omidyar, Z. Gee, and J. K. Okamuro. "Control of seed mass and seed yield by the floral homeotic gene APETALA2." Proceedings of the National Academy of Sciences 102, no. 8 (2005): 3117–22. http://dx.doi.org/10.1073/pnas.0409893102.

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40

Weigel, D. "The APETALA2 domain is related to a novel type of DNA binding domain." Plant Cell 7, no. 4 (1995): 388–89. http://dx.doi.org/10.1105/tpc.7.4.388.

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41

Chen, Xuemei, Li Zhao, and YunJu Kim. "miR172 modulates the output of the AGAMOUS/APETALA2 antagonistic pair in floral patterning." Developmental Biology 295, no. 1 (2006): 324. http://dx.doi.org/10.1016/j.ydbio.2006.04.006.

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42

Mlotshwa, Sizolwenkosi, Zhiyong Yang, YunJu Kim, and Xuemei Chen. "Floral patterning defects induced by Arabidopsis APETALA2 and microRNA172 expression in Nicotiana benthamiana." Plant Molecular Biology 61, no. 4-5 (2006): 781–93. http://dx.doi.org/10.1007/s11103-006-0049-0.

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43

Nilsson, Lars, Annelie Carlsbecker, Annika Sundås-Larsson, and Tiina Vahala. "APETALA2 like genes from Picea abies show functional similarities to their Arabidopsis homologues." Planta 225, no. 3 (2006): 589–602. http://dx.doi.org/10.1007/s00425-006-0374-1.

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44

Ripoll, J. J., A. H. K. Roeder, G. S. Ditta, and M. F. Yanofsky. "A novel role for the floral homeotic gene APETALA2 during Arabidopsis fruit development." Development 138, no. 23 (2011): 5167–76. http://dx.doi.org/10.1242/dev.073031.

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45

Tsaftaris, Athanasios S., Konstantinos Pasentsis, Panagiotis Madesis, and Anagnostis Argiriou. "Sequence Characterization and Expression Analysis of Three APETALA2-like Genes from Saffron Crocus." Plant Molecular Biology Reporter 30, no. 2 (2011): 443–52. http://dx.doi.org/10.1007/s11105-011-0355-9.

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46

Zeng, Danqi, Jaime A. Teixeira da Silva, Mingze Zhang, et al. "Genome-Wide Identification and Analysis of the APETALA2 (AP2) Transcription Factor in Dendrobium officinale." International Journal of Molecular Sciences 22, no. 10 (2021): 5221. http://dx.doi.org/10.3390/ijms22105221.

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The APETALA2 (AP2) transcription factors (TFs) play crucial roles in regulating development in plants. However, a comprehensive analysis of the AP2 family members in a valuable Chinese herbal orchid, Dendrobium officinale, or in other orchids, is limited. In this study, the 14 DoAP2 TFs that were identified from the D. officinale genome and named DoAP2-1 to DoAP2-14 were divided into three clades: euAP2, euANT, and basalANT. The promoters of all DoAP2 genes contained cis-regulatory elements related to plant development and also responsive to plant hormones and stress. qRT-PCR analysis showed t

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47

Prunet, Nathanaël, Patrice Morel, Priscilla Champelovier, et al. "SQUINT promotes stem cell homeostasis and floral meristem termination inArabidopsisthrough APETALA2 and CLAVATA signalling." Journal of Experimental Botany 66, no. 21 (2015): 6905–16. http://dx.doi.org/10.1093/jxb/erv394.

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48

Chuck, G., R. B. Meeley, and S. Hake. "The control of maize spikelet meristem fate by the APETALA2-like gene indeterminate spikelet1." Genes & Development 12, no. 8 (1998): 1145–54. http://dx.doi.org/10.1101/gad.12.8.1145.

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49

Zhou, Yan, Danfeng Lu, Canyang Li, et al. "Genetic Control of Seed Shattering in Rice by the APETALA2 Transcription Factor SHATTERING ABORTION1." Plant Cell 24, no. 3 (2012): 1034–48. http://dx.doi.org/10.1105/tpc.111.094383.

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50

WU, Yan-qing, Zhi-yuan LI, Da-qiu ZHAO, and Jun TAO. "Comparative analysis of flower-meristem-identity gene APETALA2 (AP2) codon in different plant species." Journal of Integrative Agriculture 17, no. 4 (2018): 867–77. http://dx.doi.org/10.1016/s2095-3119(17)61732-5.

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