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Journal articles on the topic 'Arabidopsis'

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Author: Grafiati

Published: 4 June 2021

Last updated: 31 July 2024

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1

Lv, Junli, Wei Wu, Tao Ma, Bohan Yang, Asaf Khan, Peining Fu, and Jiang Lu. "Kinase Inhibitor VvBKI1 Interacts with Ascorbate Peroxidase VvAPX1 Promoting Plant Resistance to Oomycetes." International Journal of Molecular Sciences 24, no. 6 (March 7, 2023): 5106. http://dx.doi.org/10.3390/ijms24065106.

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Downy mildew caused by oomycete pathogen Plasmopara viticola is a devastating disease of grapevine. P. viticola secretes an array of RXLR effectors to enhance virulence. One of these effectors, PvRXLR131, has been reported to interact with grape (Vitis vinifera) BRI1 kinase inhibitor (VvBKI1). BKI1 is conserved in Nicotiana benthamiana and Arabidopsis thaliana. However, the role of VvBKI1 in plant immunity is unknown. Here, we found transient expression of VvBKI1 in grapevine and N. benthamiana increased its resistance to P. viticola and Phytophthora capsici, respectively. Furthermore, ectopic expression of VvBKI1 in Arabidopsis can increase its resistance to downy mildew caused by Hyaloperonospora arabidopsidis. Further experiments revealed that VvBKI1 interacts with a cytoplasmic ascorbate peroxidase, VvAPX1, an ROS-scavenging protein. Transient expression of VvAPX1 in grape and N. benthamiana promoted its resistance against P. viticola, and P. capsici. Moreover, VvAPX1 transgenic Arabidopsis is more resistant to H. arabidopsidis. Furthermore, both VvBKI1 and VvAPX1 transgenic Arabidopsis showed an elevated ascorbate peroxidase activity and enhanced disease resistance. In summary, our findings suggest a positive correlation between APX activity and resistance to oomycetes and that this regulatory network is conserved in V. vinifera, N. benthamiana, and A. thaliana.

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2

Liu, Hang, Hongfei Zhu, Fei Liu, Limiao Deng, Guangxia Wu, Zhongzhi Han, and Longgang Zhao. "From Organelle Morphology to Whole-Plant Phenotyping: A Phenotypic Detection Method Based on Deep Learning." Plants 13, no. 9 (April 23, 2024): 1177. http://dx.doi.org/10.3390/plants13091177.

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The analysis of plant phenotype parameters is closely related to breeding, so plant phenotype research has strong practical significance. This paper used deep learning to classify Arabidopsis thaliana from the macro (plant) to the micro level (organelle). First, the multi-output model identifies Arabidopsis accession lines and regression to predict Arabidopsis’s 22-day growth status. The experimental results showed that the model had excellent performance in identifying Arabidopsis lines, and the model’s classification accuracy was 99.92%. The model also had good performance in predicting plant growth status, and the regression prediction of the model root mean square error (RMSE) was 1.536. Next, a new dataset was obtained by increasing the time interval of Arabidopsis images, and the model’s performance was verified at different time intervals. Finally, the model was applied to classify Arabidopsis organelles to verify the model’s generalizability. Research suggested that deep learning will broaden plant phenotype detection methods. Furthermore, this method will facilitate the design and development of a high-throughput information collection platform for plant phenotypes.

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3

Deb, Devdutta, Ryan G. Anderson, Theresa How-Yew-Kin, Brett M. Tyler, and John M. McDowell. "Conserved RxLR Effectors From Oomycetes Hyaloperonospora arabidopsidis and Phytophthora sojae Suppress PAMP- and Effector-Triggered Immunity in Diverse Plants." Molecular Plant-Microbe Interactions® 31, no. 3 (March 2018): 374–85. http://dx.doi.org/10.1094/mpmi-07-17-0169-fi.

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Effector proteins are exported to the interior of host cells by diverse plant pathogens. Many oomycete pathogens maintain large families of candidate effector genes, encoding proteins with a secretory leader followed by an RxLR motif. Although most of these genes are very divergent between oomycete species, several genes are conserved between Phytophthora species and Hyaloperonospora arabidopsidis, suggesting that they play important roles in pathogenicity. We describe a pair of conserved effector candidates, HaRxL23 and PsAvh73, from H. arabidopsidis and P. sojae respectively. We show that HaRxL23 is expressed early during infection of Arabidopsis. HaRxL23 triggers an ecotype-specific defense response in Arabidopsis, suggesting that it is recognized by a host surveillance protein. HaRxL23 and PsAvh73 can suppress pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) in Nicotiana benthamiana and effector-triggered immunity (ETI) in soybean. Transgenic Arabidopsis constitutively expressing HaRxL23 or PsAvh73 exhibit suppression of PTI and enhancement of bacterial and oomycete virulence. Together, our experiments demonstrate that these conserved oomycete RxLR effectors suppress PTI and ETI across diverse plant species.

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Shigemori, Hideyuki, Haruyuki Nakajyo, Yosuke Hisamatsu, Mitsuhiro Sekiguchi, Nobuharu Goto, and Koji Hasegawa. "Arabidopside F, a New Oxylipin from Arabidopsis thaliana." HETEROCYCLES 69, no. 1 (2006): 295. http://dx.doi.org/10.3987/com-06-s(o)33.

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5

Abe, Hiroshi, Jun Ohnishi, Mari Narusaka, Shigemi Seo, Yoshihiro Narusaka, Shinya Tsuda, and Masatomo Kobayashi. "Arabidopsis." Plant Signaling & Behavior 3, no. 7 (July 2008): 446–47. http://dx.doi.org/10.4161/psb.3.7.5556.

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6

Hisamatsu, Yosuke, Nobuharu Goto, Koji Hasegawa, and Hideyuki Shigemori. "Senescence-Promoting Effect of Arabidopside A." Zeitschrift für Naturforschung C 61, no. 5-6 (June 1, 2006): 363–66. http://dx.doi.org/10.1515/znc-2006-5-611.

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Arabidopside A isolated from Arabidopsis thaliana is a rare oxylipin, containing 12-oxophytodienoic acid (OPDA) and dinor-oxophytodienoic acid (dn-OPDA) which are known as precursors of jasmonic acid (JA) and methyl jasmonate (MeJA). The senescence-promoting effect of arabidopside A was examined by an oat (Avena sativa) leaf assay under dark or continuous light condition. Arabidopside A promoted senescence of oat leaves, and the promoting activity was more effective than for JA and OPDA, and as strong as for MeJA, which was well known to be a senescence promoter. These results suggest that arabidopside A plays important roles in leaf senescence.

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7

Murray, J., J. Larsen, T. E. Michaels, A. Schaafsma, C. E. Vallejos, and K. P. Pauls. "Identification of putative genes in bean (Phaseolus vulgaris) genomic (Bng) RFLP clones and their conversion to STSs." Genome 45, no. 6 (December 1, 2002): 1013–24. http://dx.doi.org/10.1139/g02-069.

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A set of 79 previously mapped bean (Phaseolus vulgaris) genomic (Bng) clones were partially sequenced. BLAST database searches detected homologies between 59 of these clones and genes from a variety of plants, especially Arabidopsis thaliana. Some matches in the database to the Bng clones included a putative P-glycoprotein ABC transporter from Arabidopsis, an early nodulin-binding protein (ENBP1) from Medicago truncatula, a lon-protease protein from spinach, a branched-chain amino-acid aminotransferase from Arabidopis, and a vacuolar sorting receptor (BP-80) from Pisum sativum. Additional matches were found for genes involved in isoprenoid biosynthesis, sulfur metabolism, proline biosynthesis, and floral development. Sequence tagged site (STSs) were produced for 16 of the clones, 2 of which contain simple sequence repeats (SSRs). Polymorphisms were detected for six of the STSs.Key words: CAPS, SSR, molecular markers, gene identification.

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8

Mohr, Toni J., Nicole D. Mammarella, Troy Hoff, Bonnie J. Woffenden, John G. Jelesko, and John M. McDowell. "The Arabidopsis Downy Mildew Resistance Gene RPP8 Is Induced by Pathogens and Salicylic Acid and Is Regulated by W Box cis Elements." Molecular Plant-Microbe Interactions® 23, no. 10 (October 2010): 1303–15. http://dx.doi.org/10.1094/mpmi-01-10-0022.

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Plants disease resistance (R) genes encode specialized receptors that are quantitative, rate-limiting defense regulators. R genes must be expressed at optimum levels to function properly. If expression is too low, downstream defense responses are not activated efficiently. Conversely, overexpression of R genes can trigger autoactivation of defenses with deleterious consequences for the plant. Little is known about R gene regulation, particularly under defense-inducing conditions. We examined regulation of the Arabidopsis thaliana gene RPP8 (resistance to Hyaloperonospora arabidopsidis, isolate Emco5). RPP8 was induced in response to challenge with H. arabidopsidis or application of salicylic acid, as shown with RPP8-Luciferase transgenic plants and quantitative reverse-transcription polymerase chain reaction of endogenous alleles. The RPP1 and RPP4 genes were also induced by H. arabidopsidis and salicylic acid, suggesting that some RPP genes are subject to feedback amplification. The RPP8 promoter contains three W box cis elements. Site-directed mutagenesis of all three W boxes greatly diminished RPP8 basal expression, inducibility, and resistance in transgenic plants. Motif searches indicated that the W box is the only known cis element that is statistically overrepresented in Arabidopsis nucleotide-binding leucine-rich repeat promoters. These results indicate that WRKY transcription factors can regulate expression of surveillance genes at the top of the defense-signaling cascade.

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9

Akimov, Yu. "Ultrastructure of mesophyll cells of Arabidopsis (Arabidopsis thaliana L.) after hyperthermia." Bulletin of Taras Shevchenko National University of Kyiv. Series: Biology 85, no. 2 (2021): 15–22. http://dx.doi.org/10.17721/1728_2748.2021.85.15-22.

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The influence of hyperthermia (33 ºC, 2 days) on the ultrastructure of palisade cells of mesophyll of the first rosette leaves of arabidopsis Columbia 0 ecotype (Col-0, phases 1.02–1.04) was studied. Samples of 12-day-old seedlings were selected in 2 variants: control and 2 days 33 ºC. Seedlings of the control variant were grown in a growth chamber with a photoperiod of 15/9 hours. (day/night), illumination 5.5 klx, 75 % humidity and temperature 22 ºC. In the experimental variant containers with 9-day-old seedlings were transferred for 2 days to a growth chamber with a preset light 5.5 klx and temperature 33 ºC, with a photoperiod of 15/9 hours. The conducted ultrastructural analysis allowed to reveal the spectrum of rearrangements of palisade cells after two-day action of high (33 ºC) temperature. It was shown that the high temperature negatively affected size of mesophyll palisade cells, the cross-sectional area of which was 12 % smaller than in the control. Chloroplasts show an increase in granality: in the control granas contained 6–10 thylakoids, often combining into larger granas, up to 20 or more thylakoids in the intersection zone, while after two-day hyperthermia the granas contained 20 or more thylakoids, often forming giant granas of 60 and more thylakoids, the average cross-sectional area of starch granules decreased by almost half: 0.99 μm2 compared to 1.92 μm2 in the control, the diameter of plastoglobuli increased 3–4 times: to 100–200 nm compared to 30–50 nm in the control. In mitochondria, there was a decrease in the partial volume of the cristae, enlightenment of the matrix, the cross-section of mitochondria increased at least twice: 1 μm2 compared to 0.44 μm2 in the control. The mean cross-sectional area of peroxisomes also increased at least twice, to 1.36 μm2 compared with 0.77 μm2 in the control.

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10

Somerville, Chris. "Arabidopsis Blooms." Plant Cell 1, no. 12 (December 1989): 1131. http://dx.doi.org/10.2307/3868910.

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11

Cavalieri, A. "Arabidopsis sequencing." Nature Biotechnology 14, no. 7 (July 1996): 804. http://dx.doi.org/10.1038/nbt0796-804e.

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12

Dove, Alan. "Arabidopsis database." Nature Biotechnology 18, no. 7 (July 2000): 701. http://dx.doi.org/10.1038/77207.

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13

Marshall, Andrew. "Arabidopsis sequenced." Nature Biotechnology 19, no. 1 (January 2001): 7. http://dx.doi.org/10.1038/83580.

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14

Bennetzen, Jeffrey L. "Arabidopsis arrives." Nature Genetics 27, no. 1 (January 2001): 3–5. http://dx.doi.org/10.1038/83726.

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15

Weitzman, Jonathan B. "Annotating Arabidopsis." Genome Biology 3 (2002): spotlight—20020326–02. http://dx.doi.org/10.1186/gb-spotlight-20020326-02.

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16

Somerville, C. "Arabidopsis Blooms." Plant Cell 1, no. 12 (December 1, 1989): 1131–35. http://dx.doi.org/10.1105/tpc.1.12.1131.

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17

Boutet, Stéphanie, Franck Vazquez, Jun Liu, Christophe Béclin, Mathilde Fagard, Ariane Gratias, Jean-Benoit Morel, Patrice Crété, Xuemei Chen, and Hervé Vaucheret. "Arabidopsis HEN1." Current Biology 13, no. 10 (May 2003): 843–48. http://dx.doi.org/10.1016/s0960-9822(03)00293-8.

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18

Meyerowitz, Elliot M. "Arabidopsis advances." Trends in Genetics 6 (1990): 1–2. http://dx.doi.org/10.1016/0168-9525(90)90021-w.

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19

Meyerowitz, E. M. "Arabidopsis Thaliana." Annual Review of Genetics 21, no. 1 (December 1987): 93–111. http://dx.doi.org/10.1146/annurev.ge.21.120187.000521.

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20

Grennan, Aleel K. "Arabidopsis MicroRNAs." Plant Physiology 146, no. 1 (January 2008): 3–4. http://dx.doi.org/10.1104/pp.104.900244.

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21

Anderson, Mary. "Arabidopsis Meetings." Plant Molecular Biology Reporter 13, no. 3 (September 1995): 206. http://dx.doi.org/10.1007/bf02670896.

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22

Anderson, Mary. "Arabidopsis meetings." Plant Molecular Biology Reporter 14, no. 3 (September 1996): 204. http://dx.doi.org/10.1007/bf02671654.

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23

Wixon, Jo. "Arabidopsis thaliana." Comparative and Functional Genomics 2, no. 2 (2001): 91–98. http://dx.doi.org/10.1002/cfg.75.

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Arabidopsisis universally acknowledged as the model for dicotyledonous crop plants. Furthermore, some of the information gleaned from this small plant can be used to aid work on monocotyledonous crops. Here we provide an overview of the current state of knowledge and resources for the study of this important model plant, with comments on future prospects in the field from Professor Pamela Green and Dr Sean May.

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24

Massoud, Kamal, Thierry Barchietto, Thomas Le Rudulier, Laurane Pallandre, Laure Didierlaurent, Marie Garmier, Françoise Ambard-Bretteville, Jean-Marc Seng, and Patrick Saindrenan. "Dissecting Phosphite-Induced Priming in Arabidopsis Infected with Hyaloperonospora arabidopsidis." Plant Physiology 159, no. 1 (March 9, 2012): 286–98. http://dx.doi.org/10.1104/pp.112.194647.

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25

Hisamatsu, Yosuke, Nobuharu Goto, Koji Hasegawa, and Hideyuki Shigemori. "Arabidopsides A and B, two new oxylipins from Arabidopsis thaliana." Tetrahedron Letters 44, no. 29 (July 2003): 5553–56. http://dx.doi.org/10.1016/s0040-4039(03)01148-1.

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26

IWASAKI, Norihiko, Yuko SATO, and Shigeru HISAJIMA. "Life cycle of Arabidopsis (Arabidopsis thaliana) plant in vitro." Shokubutsu Kankyo Kogaku 17, no. 1 (2005): 34–38. http://dx.doi.org/10.2525/shita.17.34.

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27

Wu, Fu-Hui, Shu-Chen Shen, Lan-Ying Lee, Shu-Hong Lee, Ming-Tsar Chan, and Choun-Sea Lin. "Tape-Arabidopsis Sandwich - a simpler Arabidopsis protoplast isolation method." Plant Methods 5, no. 1 (2009): 16. http://dx.doi.org/10.1186/1746-4811-5-16.

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28

Fahlgren, Noah, Sanjuro Jogdeo, Kristin D. Kasschau, Christopher M. Sullivan, Elisabeth J. Chapman, Sascha Laubinger, Lisa M. Smith, et al. "MicroRNA Gene Evolution in Arabidopsis lyrata and Arabidopsis thaliana." Plant Cell 22, no. 4 (April 2010): 1074–89. http://dx.doi.org/10.1105/tpc.110.073999.

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29

Maeda, Nami, Fuko Matsuta, Takaya Noguchi, Ayumu Fujii, Hikaru Ishida, Yudai Kitagawa, and Atsushi Ishikawa. "The Homeodomain–Leucine Zipper Subfamily I Contributes to Leaf Age- and Time-Dependent Resistance to Pathogens in Arabidopsis thaliana." International Journal of Molecular Sciences 24, no. 22 (November 15, 2023): 16356. http://dx.doi.org/10.3390/ijms242216356.

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In Arabidopsis thaliana (Arabidopsis), nonhost resistance (NHR) is influenced by both leaf age and the moment of inoculation. While the circadian clock and photoperiod have been linked to the time-dependent regulation of NHR in Arabidopsis, the mechanism underlying leaf age-dependent NHR remains unclear. In this study, we investigated leaf age-dependent NHR to Pyricularia oryzae in Arabidopsis. Our findings revealed that this NHR type is regulated by both miR156-dependent and miR156-independent pathways. To identify the key players, we utilized rice-FOX Arabidopsis lines and identified the rice HD-Zip I OsHOX6 gene. Notably, OsHOX6 expression confers robust NHR to P. oryzae and Colletotrichum nymphaeae in Arabidopsis, with its effect being contingent upon leaf age. Moreover, we explored the role of AtHB7 and AtHB12, the Arabidopsis closest homologues of OsHOX6, by studying mutants and overexpressors in Arabidopsis–C. higginsianum interaction. AtHB7 and AtHB12 were found to contribute to both penetration resistance and post-penetration resistance to C. higginsianum in a leaf age- and time-dependent manner. These findings highlight the involvement of HD-Zip I AtHB7 and AtHB12, well-known regulators of development and abiotic stress responses, in biotic stress responses in Arabidopsis.

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30

Taji, Teruaki, Motoaki Seki, Masakazu Satou, Tetsuya Sakurai, Masatomo Kobayashi, Kanako Ishiyama, Yoshihiro Narusaka, Mari Narusaka, Jian-Kang Zhu, and Kazuo Shinozaki. "Comparative Genomics in Salt Tolerance between Arabidopsis and Arabidopsis-Related Halophyte Salt Cress Using Arabidopsis Microarray." Plant Physiology 135, no. 3 (July 2004): 1697–709. http://dx.doi.org/10.1104/pp.104.039909.

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31

Widemann, Emilie, Kristie Bruinsma, Brendan Walshe-Roussel, Cristina Rioja, Vicent Arbona, Repon Kumer Saha, David Letwin, et al. "Multiple indole glucosinolates and myrosinases defend Arabidopsis against Tetranychus urticae herbivory." Plant Physiology 187, no. 1 (June 19, 2021): 116–32. http://dx.doi.org/10.1093/plphys/kiab247.

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Abstract Arabidopsis (Arabidopsis thaliana) defenses against herbivores are regulated by the jasmonate (JA) hormonal signaling pathway, which leads to the production of a plethora of defense compounds. Arabidopsis defense compounds include tryptophan-derived metabolites, which limit Arabidopsis infestation by the generalist herbivore two-spotted spider mite, Tetranychus urticae. However, the phytochemicals responsible for Arabidopsis protection against T. urticae are unknown. Here, we used Arabidopsis mutants disrupted in the synthesis of tryptophan-derived secondary metabolites to identify phytochemicals involved in the defense against T. urticae. We show that of the three tryptophan-dependent pathways found in Arabidopsis, the indole glucosinolate (IG) pathway is necessary and sufficient to assure tryptophan-mediated defense against T. urticae. We demonstrate that all three IGs can limit T. urticae herbivory, but that they must be processed by myrosinases to hinder T. urticae oviposition. Putative IG breakdown products were detected in mite-infested leaves, suggesting in planta processing by myrosinases. Finally, we demonstrate that besides IGs, there are additional JA-regulated defenses that control T. urticae herbivory. Together, our results reveal the complexity of Arabidopsis defenses against T. urticae that rely on multiple IGs, specific myrosinases, and additional JA-dependent defenses.

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32

Cooper, A. J., A. O. Latunde-Dada, A. Woods-Tör, J. Lynn, J. A. Lucas, I. R. Crute, and E. B. Holub. "Basic Compatibility of Albugo candida in Arabidopsis thaliana and Brassica juncea Causes Broad-Spectrum Suppression of Innate Immunity." Molecular Plant-Microbe Interactions® 21, no. 6 (June 2008): 745–56. http://dx.doi.org/10.1094/mpmi-21-6-0745.

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A biotrophic parasite often depends on an intrinsic ability to suppress host defenses in a manner that will enable it to infect and successfully colonize a susceptible host. If the suppressed defenses otherwise would have been effective against alternative pathogens, it follows that primary infection by the “suppressive” biotroph potentially could enhance susceptibility of the host to secondary infection by avirulent pathogens. This phenomenon previously has been attributed to true fungi such as rust (basidiomycete) and powdery mildew (ascomycete) pathogens. In our study, we observed broad-spectrum suppression of host defense by the oomycete Albugo candida (white blister rust) in the wild crucifer Arabidopsis thaliana and a domesticated relative, Brassica juncea. A. candida subsp. arabidopsis suppressed the “runaway cell death” phenotype of the lesion mimic mutant lsd1 in Arabidopsis thaliana in a sustained manner even after subsequent inoculation with avirulent Hyaloperonospora arabidopsis (Arabidopsis thaliana downy mildew). In sequential inoculation experiments, we show that preinfection by virulent Albugo candida can suppress disease resistance in cotyledons to several downy mildew pathogens, including contrasting examples of genotype resistance to H. arabidopsis in Arabidopsis thaliana that differ in the R protein and modes of defense signaling used to confer the resistance; genotype specific resistance in B. juncea to H. parasitica (Brassica downy mildew; isolates derived from B. juncea); species level (nonhost) resistance in both crucifers to Bremia lactucae (lettuce downy mildew) and an isolate of the H. parasitica race derived from Brassica oleracea; and nonhost resistance in B. juncea to H. arabidopsis. Broad-spectrum powdery mildew resistance conferred by RPW8 also was suppressed in Arabidopsis thaliana to two morphotypes of Erysiphe spp. following pre-infection with A. candida subsp. arabidopsis.

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33

Goldwasser, Yaakov, Dina Plakhine, and John I. Yoder. "Arabidopsis thalianasusceptibility toOrobanchespp." Weed Science 48, no. 3 (May 2000): 342–46. http://dx.doi.org/10.1614/0043-1745(2000)048[0342:wbae]2.0.co;2.

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34

Abel, Steffen, Miguel Blazquez, Jeffery Dangl, Xing Wang Deng, Ian Graham, John Harada, Jonathan Jones, and Ove Nilsson. "Arabidopsis Research 2000." Plant Cell 12, no. 12 (December 2000): 2302. http://dx.doi.org/10.2307/3871230.

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35

Eckardt, Nancy A., Takashi Araki, Christoph Benning, Pilar Cubas, Justin Goodrich, Steven E. Jacobsen, Patrick Masson, et al. "Arabidopsis Research 2001." Plant Cell 13, no. 9 (September 2001): 1973. http://dx.doi.org/10.2307/3871421.

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36

Scheres, Ben, and John Browse. "Playing with Arabidopsis." Plant Physiology 126, no. 2 (June 1, 2001): 468–70. http://dx.doi.org/10.1104/pp.126.2.468.

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37

Rodermel, Steven. "Arabidopsis Variegation Mutants." Arabidopsis Book 1 (January 2002): e0079. http://dx.doi.org/10.1199/tab.0079.

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38

Terzi, Lionel C., and Gordon G. Simpson. "Arabidopsis RNA immunoprecipitation." Plant Journal 59, no. 1 (July 2009): 163–68. http://dx.doi.org/10.1111/j.1365-313x.2009.03859.x.

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39

Ausubel, Fred, and Philip Benfey. "Arabidopsis Functional Genomics." Plant Physiology 129, no. 2 (June 1, 2002): 393. http://dx.doi.org/10.1104/pp.900036.

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40

Tena, Guillaume. "Arabidopsis proteome v2.0." Nature Plants 6, no. 4 (April 2020): 330. http://dx.doi.org/10.1038/s41477-020-0651-1.

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41

Abel, Steffen, Miguel Blázquez, Jeffery Dangl, Xing Wang Deng, Ian Graham, John Harada, Jonathan Jones, and Ove Nilsson. "Arabidopsis Research 2000." Plant Cell 12, no. 12 (December 2000): 2302–9. http://dx.doi.org/10.1105/tpc.12.12.2302.

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42

Eckardt, Nancy A., Takashi Araki, Christoph Benning, Pilar Cubas, Justin Goodrich, Steven E. Jacobsen, Patrick Masson, et al. "Arabidopsis Research 2001." Plant Cell 13, no. 9 (September 2001): 1973–82. http://dx.doi.org/10.1105/tpc.13.9.1973.

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43

Preuss, D. "Cultivation of Arabidopsis." Cold Spring Harbor Protocols 2006, no. 27 (October 1, 2006): pdb.ip22. http://dx.doi.org/10.1101/pdb.ip22.

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44

Fernandez-Calvino, Lourdes, Christine Faulkner, John Walshaw, Gerhard Saalbach, Emmanuelle Bayer, Yoselin Benitez-Alfonso, and Andrew Maule. "Arabidopsis Plasmodesmal Proteome." PLoS ONE 6, no. 4 (April 20, 2011): e18880. http://dx.doi.org/10.1371/journal.pone.0018880.

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45

Fluet, Amy. "All about Arabidopsis." Current Biology 10, no. 13 (June 2000): R468. http://dx.doi.org/10.1016/s0960-9822(00)00572-8.

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46

de Vries, G. E. "Arabidopsis thermotolerance mutants." Trends in Plant Science 5, no. 7 (July 2000): 276. http://dx.doi.org/10.1016/s1360-1385(00)01705-2.

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47

Mckay, D. "Arabidopsis genome sequenced." Trends in Biotechnology 19, no. 2 (February 2001): 42. http://dx.doi.org/10.1016/s0167-7799(00)01560-2.

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48

Phillips, Andrew L. "Gibberellins in Arabidopsis." Plant Physiology and Biochemistry 36, no. 1-2 (January 1998): 115–24. http://dx.doi.org/10.1016/s0981-9428(98)80096-x.

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49

Fray, Rupert G., and Gordon G. Simpson. "The Arabidopsis epitranscriptome." Current Opinion in Plant Biology 27 (October 2015): 17–21. http://dx.doi.org/10.1016/j.pbi.2015.05.015.

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Casci, Tanita. "Arabidopsis' hidden potential." Nature Reviews Genetics 9, no. 4 (April 2008): 248. http://dx.doi.org/10.1038/nrg2350.

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