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Prot-Class: A bioinformatics tool for protein classification based on amino acid signatures  [PDF]
Jens Lichtenberg, Brian D. Keppler, Thomas Conley, Dazhang Gu, Paul Burns, Lonnie R. Welch, Allan M. Showalter
Natural Science (NS) , 2012, DOI: 10.4236/ns.2012.412A141
Abstract:

Knowledge about characteristics shared across known members of a protein family enables their identification within the complete set of proteins in an organism. Shared features are usually expressed through motifs, which can incorporate specific patterns and even amino acid (AA) biases. Based on a set of classification patterns and biases it can be determined which additional proteins may belong to a specific family and share its functionality. A bioinformatics tool (Prot-Class) was implemented to examine protein sequences and characterize them based upon user-defined AA composition percentages and user defined AA patterns. In addition the tool allows for the identification of repeated AA patterns, biased AA compositions within windows of user-defined length, and the characteristics of putative signal peptides and glycosylphosphatidylinositol (GPI) lipid anchors. ProtClass is general purpose and can be applied to analyze protein sequences from any organism. The Prot-Class source code is available through the GNU General Public License v3 and can be accessed via the Google Code Repository: http://code.google.com/p/prot-class/.

GENES OF ARABIDOPSIS THALIANA INVOLVED IN WAX METABOLISM
ROXANA-IULIANA TEODOR,AL. YEPHREMOV
Scientific Annals of Alexandru Ioan Cuza University of Iasi. New Series, Section 2. Vegetal Biology , 2008,
Abstract: The aerial surfaces of land plants are covered with cuticle that acts as a barrier providing protection against water loss, pathogen invasion and other environmental aggressions. Besides physical and chemical barriers, such as a waxy cuticle, plant defense mechanisms also involve a coordinated activation of cellular responses to limit damage. The eceriferum (cer) mutants of Arabidopsis define multiple genes required for various steps in cuticular wax biosynthesis, transport and regulation of lipid-related pathways. Although the basic biochemistry of wax production has been elucidated, very little is known about its regulation and its contribution to the natural immunity. This review presents recently cloned wax biosynthetic genes and discusses regulatory aspects of wax biosynthesis.
A rapid method for isolation of low-molecular-weight RNA from Arabidopsis using low salt concentration buffer
Han Cheng,Jing Gao,Zewei An,Huasun Huang
International Journal of Plant Biology , 2010, DOI: 10.4081/pb.2010.e14
Abstract:
Defining the Plant Peroxisomal Proteome: From Arabidopsis to Rice
Navneet Kaur,Jianping Hu
Frontiers in Plant Science , 2011, DOI: 10.3389/fpls.2011.00103
Abstract: Peroxisomes are small subcellular organelles mediating a multitude of processes in plants. Proteomics studies over the last several years have yielded much needed information on the composition of plant peroxisomes. In this review, the status of peroxisome proteomics studies in Arabidopsis and other plant species and the cumulative advances made through these studies are summarized. A reference Arabidopsis peroxisome proteome is generated, and some unique aspects of Arabidopsis peroxisomes that were uncovered through proteomics studies and hint at unanticipated peroxisomal functions are also highlighted. Knowledge gained from Arabidopsis was utilized to compile a tentative list of peroxisome proteins for the model monocot plant, rice. Differences in the peroxisomal proteome between these two model plants were drawn, and novel facets in rice were expounded upon. Finally, we discuss about the current limitations of experimental proteomics in decoding the complete and dynamic makeup of peroxisomes, and complementary and integrated approaches that would be beneficial to defining the peroxisomal metabolic and regulatory roadmaps. The synteny of genomes in the grass family makes rice an ideal model to study peroxisomes in cereal crops, in which these organelles have received much less attention, with the ultimate goal to improve crop yield.
QTL for floral stem lignin content and degradability in three recombinant inbred line (RIL) progenies of Arabidopsis thaliana and search for candidate genes involved in cell wall biosynthesis and degradability  [PDF]
H. Chavigneau, N. Goué, S. Delaunay, A. Courtial, L. Jouanin, M. Reymond, V. Méchin, Y. Barrière
Open Journal of Genetics (OJGen) , 2012, DOI: 10.4236/ojgen.2012.21002
Abstract: Deciphering the genetic determinants involved in cell wall assembly is a strategic issue for breeding programs that target both ruminant feeding and biofuel production. The Arabidopsis thaliana model system has great potentials to elucidate the genetic determinants involved in cell wall component biosynthesis and those involved in the regulation cascades allowing their coordinated assembly. QTL for biomass quality related traits (cell wall content, lignin content, and cell wall degradability) were mapped in the three Arabidopsis RIL progenies Bay0 × Shahdara, Bur0 × Col0, and Blh1 × Col0. Overall, 40 QTL were detected for these traits, explaining up to 33 and 12% of the observed phenotypic variation for lignin content and cell wall degradability respectively. Major QTL hotspots were mapped on chromosome 1 (position 5 Mbp), chromosome 4 (position 1 Mbp), and chromosome 5 (position 3 Mbp). A putative candidate gene set (82 genes) was considered including those previously described as involved in cell wall phenolic component biosynthesis, their regulation factors, and genes involved in lignified tissue patterning. Colocalisations observed (according to the reference sequence of Col0) between the detected QTL and these candidate genes did not prioritize any of the three gene groups (monolignol biosynthesis, transcription factors, lignified tissue patterning). Colocalizations were thus observed for 57% of monolignol biosynthesis related genes, 55% of the transcription factors considered, and 66% of genes considered to be involved in lignified tissue patterning and assembly. Colocalizations were observed for at least one member of all investigated gene families, except WRKY transcription factors. Colocalizations were also shown with several miRNA putatively involved in the regulation of lignifying tissue assembly. Taking into account the QTL shown in the Bur0 × Col0 progeny, allelic variations were shown in the MYB32, MYB58, MYB75, GRAS SCARECROW, AtC3H14 zinc finger, SHINE2, and IFL1 genes and in the AtMIR397a. Given that the list of candidate genes is not complete, and because the QTL support intervals encompassed genes of still unknown function, it is still not clear whether one of the selected candidates is responsible for the effect of a detected QTL. Mutant investigation and positional cloning steps are likely essential to clearly determine the causal mechanism involved in cell wall degradability variation.
Interactions of Auxinic Compounds on Ca2+ Signaling and Root Growth in Arabidopsis thaliana  [PDF]
Neal D. Teaster, Jeffrey A. Sparks, Elison B. Blancaflor, Robert E. Hoagland
American Journal of Plant Sciences (AJPS) , 2015, DOI: 10.4236/ajps.2015.619294
Abstract: Auxinic-like compounds have been widely used as weed control agents. Over the years, the modes of action of auxinic herbicides have been elucidated, but most studies thus far have focused on their effects on later stages of plant growth. Here, we show that some select auxins and auxiniclike herbicides trigger a rapid elevation in root cytosolic calcium levels within seconds of application. Arabidopsis thaliana plants expressing the Yellow-Cameleon (YC) 3.60 calcium reporter were treated with indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), 1-naphthalene acetic acid (NAA), and two synthetic herbicides, 2,4-dichlorophenoxyacetic acid (2,4-D) and mecoprop [2-(4-chloro- 2-methylphenoxy) propanoic acid], followed by monitoring cytosolic calcium changes over a 10 minute time course. Seconds after application of compounds to roots, the Ca2+ signaling-mediated pathway was triggered, initiating the plant response to these compounds as monitored and recorded using Fluorescence Resonance Energy Transfer (FRET)-sensitized emission imaging. Each compound elicited a specific and unique cytosolic calcium signature. Also primary root development and elongation was greatly reduced or altered when exposed at two concentrations (0.10 and 1.0 μM) of each compound. Within 20 to 25 min after triggering of the Ca2+ signal, root growth inhibition could be detected. We speculate that differences in calcium signature among the tested auxins and auxinic herbicides might correlate with their variation and potency with regard to root growth inhibition.
An Artemisia WD40-Repeat Gene Regulates Multiple Cellular Functions in Arabidopsis  [PDF]
Wei Wang, Qing Zhang, Dianjing Guo
Journal of Biosciences and Medicines (JBM) , 2016, DOI: 10.4236/jbm.2016.45003
Abstract: In this study, we isolated a WD40-repeat gene from Artemisia annua glandular trichomes. This gene shows 69.97% sequence similarity to Arabidopsis TTG1 at aminoacid level. Sub-cellular localization study shows that AaWD40 protein diffuses in both cell nucleus and cytosol. The correct nuclear localization of AaWD40 was observed when co-expressed with AabHLH, a putative A. thaliana AtTTG1 homologue cloned from Artemisia annua glandular trichomes. When AaWD40 gene was ectopically over expressed in Arabidopsis transparent testa glabrous1-1 (ttg1-1) mutants of A. thaliana, PAs production in seeds was restored, and the trichomeless phenotypes of mutant were rescued. Real-time PCR analysis results revealed that ETC1, CPC, TTG2 and BAN (the downstream targets of AtTTG1 depend on regulatory complex), which regulate the epidermal differentiation and anthocyanin biosynthesis were differentially expressed as a result of AaWD40 over expression. Furthermore, the CLV1, CLV2, CLV3 and WUS, which are required to maintain the stem-cell niche of Arabidopsis shoot apex, were also modulated by AaWD40 and Arabidopsis TTG1. The transcriptions of AP2/ERF, bHLH, MYB, WRKY and NACs family proteins, which are mostly involved in defense, stress response and development regulation, were remarkably modulated by AaWD40 over expression. We hypothesize that WD40 repeat proteins act as a crucial factor in regulating a wide variety of cellular functions in A. thaliana.
Adaptation of Arabidopsis Plants to Tropical Aeroponics Using Cool Root Zone Temperatures  [PDF]
Sandhya Srikanth, Tsui Wei Choong, Jiashu Chu, Jie He, Zhong Chen
American Journal of Plant Sciences (AJPS) , 2017, DOI: 10.4236/ajps.2017.813222
Abstract:

Arabidopsis thaliana (L.) Heyhn. is a well known model plant in plant research. However, its growth conditions and diminutive stature associated with low biomass at maturity make it a challenging species for physiological studies. While in the tropical countries, it can only be grown either by tissue cultures or in growth chambers under controlled conditions. An aeroponic technique with 20°C ± 2°C and 30°C ± 2°C root-zone temperatures (RZT) was used to grow Arabidopsis (Columbia ecotype) in a tropical greenhouse with natural irradiance and high ambient temperature (38°C/28°C day/night). Seedlings germinated in growth chambers at 20°C or 30°C. At 6 to 8 leaf stage, they were transferred to the aeroponic troughs with their roots exposed to constant temperature of 20°C ± 2°C and 30°C ± 2°C while their aerial parts were subjected to fluctuating ambient temperature from 28°C to 38°C. After a week, plants have acclimatised to both RZTs and started developing normal rosettes, bolted and yielded viable seeds. However, 20°C ± 2°C RZT allowed them to recover from turgor pressure despite of wilting, and significantly increased biomass. Mature plants grown in each RZTs were compared morphologically and physiologically to the plants grown in growth chamber (GC) at 20°C (root and shoot) temperature with 60% relative humidity. Aeroponically grown plants did not experience photoinhibition, and also exhibited higher photosynthetic light usage efficiency and higher capacities of heat dissipation, compared to GC plants. This aeroponics with cool RZTs can allow the use of Arabidopsis as a model plant even under tropical climate.

Glucosinolates and Their Hydrolysis Products in Arabidopsis thaliana Influence Performance and Feeding Choice of Pieris rapae and Spodoptera exigua  [PDF]
Julie A. Kemarly-Dowland, Maria Gabriela Bidart
Advances in Entomology (AE) , 2023, DOI: 10.4236/ae.2023.114020
Abstract: Glucosinolates and their hydrolysis products, found in plants of the order Brassicales, are well-known for their defensive properties against insect herbivores. Arabidopsis thaliana (Col-0) genetic lines with mutations that modify the type of glucosinolates (i.e. myb28myb29 and cyp79B2cyp79B3 are deficient in the production of aliphatic and indolyl glucosinolates, respectively) make it possible to test for the specific effects of these secondary chemicals on insect herbivores. The Pad3 mutant (deficient in camalexin), which has a role in resistance to pathogens, was also tested. Likewise, the effects of different glucosinolate hydrolysis products can be evaluated using genetically modified (GM) lines of the wild type Col-0 ecotype, which naturally produces isothiocyanates. These GM lines include the nitrile-producing 35S: ESP and the double knockout tgg1tgg2, which virtually lacks hydrolysis products. In both no-choice and choice experiments, the crucifer specialist Pieris rapae was virtually unaffected by differences in the type of glucosinolates or hydrolysis products. In contrast, the generalist insect Spodoptera exigua had statistically significant increases in pupae/adult weight and faster developmental times when reared on mutants deficient in the production of aliphatic and indolyl glucosinolates and their hydrolysis products. There were no differences in the performance of either insect species when reared on wild type Col-0 or Pad3. Results from feeding choice trials showed that Pieris rapae had no statistically significant preference for any of the genetic lines. In contrast, Spodoptera exigua had a significant feeding preference for the double mutant tgg1tgg2. This study provides evidence that variation in the type of glucosinolates and their hydrolysis products can influence insect performance and feeding choices, and that responses are species-specific.
Dissecting Multiple Arabidopsis CC-NBS-LRR Proteins Structure and Localization  [PDF]
Jianzhong Huang, Xiuying Guan, Xiaoju Zhong, Peng Jia, Hongbin Zhang, Kai Chen, Zhuojun Li, Guangyu Chen, Chuitang Zeng
Journal of Biosciences and Medicines (JBM) , 2024, DOI: 10.4236/jbm.2024.127008
Abstract: NBS-LRR (nucleotide binding sites and leucine rich repeat) protein plays a crucial role as sentries and as defense activators in plants. The structure and function of NBS-LRR proteins are closely related. Previous articles have announced that the activated ZAR1 (HopZ-Activated Resistance 1) forms a pentamer in the plasma membrane, which is a calcium permeable channel that can trigger plant immune signaling and cell death. However, the structure of galore NBS-LRRs in Arabidopsis is not yet clear. The functional sites of distinct NBS-LRR in cells may vary. In addition, identifying pathogens and activating defense regions may occur in different subcellular compartments. Therefore, dissecting the specific structure and positioning of NBS-LRRs is an indispensable step in understanding their functions. In this article, we exploit AlphaFold to predict the structure of some designed NBS-LRRs, and utilize Agroinfiltration transient expression system, combined with biochemical fractionation, to dissect the localization of these NBS-LRR receptors from Arabidopsis. Structural data indicates that the identified NBS-LRRs share analogous conformation. Membrane fractionation assay demonstrates these NBS-LRRs are mainly associated with the membrane. These data show that the Ca2+-permeable channel activity may be evolutionarily conserved in NBS-LRR of Arabidopsis, and this study provides some reference clues for analyzing the structure and localization patterns of other plant immune receptors.
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