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1.
Article in English | MEDLINE | ID: mdl-33431582

ABSTRACT

Throughout plant development, vascular cells continually form from within a population of seemingly equivalent cells. Vascular cells connect end to end to form continuous strands, and vascular strands connect at both or either end to form networks of exquisite complexity and mesmerizing beauty. Here we argue that experimental evidence gained over the past few decades implicates the plant hormone auxin-its production, transport, perception, and response-in all the steps that lead to the patterned formation of the plant vascular system, from the formation of vascular cells to their connection into vascular networks. We emphasize the organizing principles of the cell- and tissue-patterning process, rather than its molecular subtleties. In the picture that emerges, cells compete for an auxin-dependent, cell-polarizing signal; positive feedback between cell polarization and cell-to-cell movement of the polarizing signal leads to gradual selection of cell files; and selected cell files differentiate into vascular strands that drain the polarizing signal from the neighboring cells. Although the logic of the patterning process has become increasingly clear, the molecular details remain blurry; the future challenge will be to bring them into razor-sharp focus.


Subject(s)
Indoleacetic Acids/metabolism , Plant Development , Plant Vascular Bundle/growth & development , Plants/metabolism , Body Patterning , Plant Vascular Bundle/metabolism
2.
Dev Dyn ; 249(9): 1127-1146, 2020 09.
Article in English | MEDLINE | ID: mdl-32319191

ABSTRACT

BACKGROUND: Understanding developmental processes requires the unambiguous identification of cells and tissues, and the selective manipulation of the properties of those cells and tissues. Both requirements can most efficiently be satisfied through the use of GAL4/GFP enhancer-trap lines. No such lines, however, have been characterized for the study of early leaf development in the Columbia-0 reference genotype of Arabidopsis. RESULTS: Here we address this limitation by identifying and characterizing a set of GAL4/GFP enhancer-trap lines in the Columbia-0 background for the specific labeling of cells and tissues during early leaf development, and for the targeted expression of genes of interest in those cells and tissues. CONCLUSIONS: By using one line in our set to address outstanding questions in leaf vein patterning, we show that these lines can be used to address key questions in plant developmental biology.


Subject(s)
Arabidopsis , Enhancer Elements, Genetic , Gene Expression Regulation, Plant , Green Fluorescent Proteins , Plant Leaves , Plants, Genetically Modified , Arabidopsis/embryology , Arabidopsis/genetics , Green Fluorescent Proteins/biosynthesis , Green Fluorescent Proteins/genetics , Place Cells/metabolism , Plant Leaves/embryology , Plant Leaves/genetics , Plants, Genetically Modified/embryology , Plants, Genetically Modified/genetics
3.
Planta ; 247(6): 1267-1276, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29453664

ABSTRACT

MAIN CONCLUSION: Based on yeast one-hybrid assays, we show that the presence of C-terminal AHA motifs is not a prerequisite for transactivation potential in rice heat shock factors. Transcriptional activation or transactivation (TA) of heat stress responsive genes takes place by binding of heat shock factors (Hsfs) to heat shock elements. Analysis of TA potential of thirteen rice (Oryza sativa L.) Hsfs (OsHsfs) carried out in this study by yeast one-hybrid assay showed that OsHsfsA3 possesses strong TA potential while OsHsfs A1a, A2a, A2b, A4a, A4d, A5, A7b, B1, B2a, B2b, B2c and B4d lack TA potential. From a near complete picture of TA potential of the OsHsf family (comprising of 25 members) emerging from this study and an earlier report from our group (Mittal et al. in FEBS J 278(17):3076-3085, 2011), it is concluded that (1) overall, six OsHsfs, namely A3, A6a, A6b, A8, C1a and C1b possess TA potential; (2) four class A OsHsfs, namely A3, A6a, A6b and A8 have TA potential out of which A6a and A6b contain AHA motifs while A3 and A8 lack AHA motifs; (3) nine class A OsHsfs, namely A1a, A2a, A2b, A2e, A4a, A4d, A5, A7a and A7b containing AHA motif(s) lack TA function in the yeast assay system; (4) all class B OsHsfs lack AHA motifs and TA potential (B4a not analyzed) and (5) though all class C OsHsf members lack AHA motifs, two members C1a and C1b possess TA function, while one member C2a lacks TA potential (C2b not analyzed). Thus, the presence or absence of AHA motif is possibly not the only factor determining TA potential of OsHsfs. Our findings will help to identify the transcriptional activators of rice heat shock response.


Subject(s)
Gene Expression Regulation, Plant , Heat Shock Transcription Factors/metabolism , Oryza/genetics , Transcriptional Activation , Genes, Reporter , Heat Shock Transcription Factors/genetics , Heat-Shock Response , Oryza/physiology , Plant Proteins/genetics , Plant Proteins/metabolism , Two-Hybrid System Techniques
4.
Saudi J Biol Sci ; 23(2): 243-7, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26981006

ABSTRACT

Heat stress adversely affects the growth and yield of faba bean crop. Accumulation of ClpB/Hsp100 class of proteins is a critical parameter in induction of acquired heat stress tolerance in plants. Heat-induced expression of ClpB/Hsp100 genes has been noted in diverse plant species. Using primers complementary to soybean ClpB/Hsp100 gene, we analyzed the transcript expression profile of faba bean ClpB/Hsp100 gene in leaves of seedlings and flowering plants and in pollen grains. ClpB/Hsp100 protein accumulation profile was analyzed in leaves of faba bean seedlings using Arabidopsis thaliana cytoplasmic Hsp101 antibodies. The transcript and protein levels of faba bean ClpB/Hsp100 were significantly induced in response to heat stress.

5.
Plant Physiol Biochem ; 86: 100-108, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25438142

ABSTRACT

Climate change is resulting in heightened incidences of plant heat stress episodes. Production of transgenic crops with enhanced heat stress tolerance is a highly desired agronomic trait for the sustainability of food production in 21st century. We review the current status of our understanding of the high temperature stress response of plants. We specifically deliberate on the progress made in altering levels of heat shock proteins (Hsp100, Hsp70/Hsp40 and sHsps), heat shock factors and specific metabolic proteins in improving plant tolerance to heat stress by transgenic approach.


Subject(s)
Adaptation, Physiological/genetics , Climate Change , Climate , Crops, Agricultural/genetics , Hot Temperature , Agriculture/methods , Agriculture/trends , Biomass , Crops, Agricultural/growth & development , Crops, Agricultural/metabolism , Gene Expression Regulation, Plant , Heat-Shock Proteins/genetics , Heat-Shock Proteins/metabolism , Plants, Genetically Modified
6.
Plant Sci ; 205-206: 38-47, 2013 May.
Article in English | MEDLINE | ID: mdl-23498861

ABSTRACT

Production of plants tolerant to high temperature stress is of immense significance in the light of global warming and climate change. Plant cells respond to high temperature stress by re-programming their genetic machinery for survival and reproduction. High temperature tolerance in transgenic plants has largely been achieved either by over-expressing heat shock protein genes or by altering levels of heat shock factors that regulate expression of heat shock and non-heat shock genes. Apart from heat shock factors, over-expression of other trans-acting factors like DREB2A, bZIP28 and WRKY proteins has proven useful in imparting high temperature tolerance. Besides these, elevating the genetic levels of proteins involved in osmotic adjustment, reactive oxygen species removal, saturation of membrane-associated lipids, photosynthetic reactions, production of polyamines and protein biosynthesis process have yielded positive results in equipping transgenic plants with high temperature tolerance. Cyclic nucleotide gated calcium channel proteins that regulate calcium influxes across the cell membrane have recently been shown to be the key players in induction of high temperature tolerance. The involvement of calmodulins and kinases in activation of heat shock factors has been implicated as an important event in governing high temperature tolerance. Unfilled gaps limiting the production of high temperature tolerant transgenic plants for field level cultivation are discussed.


Subject(s)
Gene Expression Regulation, Plant , Plant Physiological Phenomena , Plants, Genetically Modified/physiology , Plants/genetics , Arabidopsis/genetics , Arabidopsis/metabolism , Arabidopsis/physiology , Gene Expression , Heat-Shock Proteins/genetics , Heat-Shock Response/genetics , Hot Temperature , Plant Proteins/genetics , Plant Proteins/metabolism , Plant Proteins/physiology , Plants, Genetically Modified/genetics , Signal Transduction , Stress, Physiological , Trans-Activators/genetics , Trans-Activators/metabolism
7.
Cell Stress Chaperones ; 17(2): 243-54, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22147560

ABSTRACT

ClpB-cytoplasmic (ClpB-cyt)/Hsp100 is an important chaperone protein in rice. Cellular expression of OsClpB-cyt transcript is governed by heat stress, metal stress, and developmental cues. Transgenic rice plants produced with 2 kb OsClpB-cyt promoter driving Gus reporter gene showed heat- and metal-regulated Gus expression in vegetative tissues and constitutive Gus expression in calli, flowering tissues, and embryonal half of seeds. Rice seedlings regenerated with OsClpB-cyt promoter fragment with deletion of its canonical heat shock element sequence (HSE(-273 to -280)) showed not only heat shock inducibility of Gus transcript/protein but also constitutive expression of Gus in vegetative tissues. It thus emerges that the only classical HSE present in OsClpB-cyt promoter is involved in repressing expression of OsClpB-cyt transcript under unstressed control conditions. Yeast one-hybrid assays suggested that OsHsfA2c specifically interacts with OsClpB-cyt promoter. OsHsfA2c also showed binding with OsClpB-cyt and OsHsfB4b showed binding with OsClpB-cyt; notably, interaction of OsHsfB4b was seen for all three OsClpB/Hsp100 protein isoforms (i.e., ClpB-cytoplasmic, ClpB-mitochondrial, and ClpB-chloroplastic). Furthermore, OsHsfB4b showed interaction with OsHsfA2c. This study suggests that OsHsfA2c may play a role as transcriptional activator and that OsHsfB4b is an important part of this heat shock responsive circuitry.


Subject(s)
DNA-Binding Proteins/genetics , DNA-Binding Proteins/metabolism , Gene Expression Regulation, Plant , Genes, Plant , Heat-Shock Proteins/genetics , Heat-Shock Proteins/metabolism , Oryza/genetics , Oryza/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Promoter Regions, Genetic/genetics , Transcription Factors/genetics , Transcription Factors/metabolism , Heat Shock Transcription Factors , Mutation , Plants, Genetically Modified , Protein Binding
8.
FEBS J ; 278(17): 3076-85, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21729241

ABSTRACT

Binding of heat shock factors (Hsfs) to heat shock elements (HSEs) leads to transcriptional regulation of heat shock genes. Genome-wide, 953 rice genes contain perfect-type, 695 genes gap-type and 1584 genes step-type HSE sequences in their 1-kb promoter region. The rice genome contains 13 class A, eight class B and four class C Hsfs (OsHsfs) and has OsHsf26 (which is of variant type) genes. Chemical cross-linking analysis of in vitro synthesized OsHsf polypeptides showed formation of homotrimers of OsHsfA2c, OsHsfA9 and OsHsfB4b proteins. Binding analysis of polypeptides with oligonucleotide probes containing perfect-, gap-, and step-type HSE sequences showed that OsHsfA2c, OsHsfA9 and OsHsfB4b differentially recognize various model HSEs as a function of varying reaction temperatures. The homomeric form of OsHsfA2c and OsHsfB4b proteins was further noted by the bimolecular fluorescence complementation approach in onion epidermal cells. In yeast two-hybrid assays, OsHsfB4b showed homomeric interaction as well as distinct heteromeric interactions with OsHsfA2a, OsHsfA7, OsHsfB4c and OsHsf26. Transactivation activity was noted in OsHsfA2c, OsHsfA2d, OsHsfA9, OsHsfC1a and OsHsfC1b in yeast cells. These differential patterns pertaining to binding with HSEs and protein-protein interactions may have a bearing on the cellular functioning of OsHsfs under a range of different physiological and environmental conditions.


Subject(s)
DNA-Binding Proteins/metabolism , Heat-Shock Proteins/metabolism , Oryza/metabolism , Plant Proteins/metabolism , Response Elements , Transcription Factors/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Cells, Cultured , Cross-Linking Reagents/chemistry , DNA, Plant/metabolism , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/genetics , Electrophoretic Mobility Shift Assay , Genes, Plant , Heat Shock Transcription Factors , Heat-Shock Proteins/chemistry , Heat-Shock Proteins/genetics , Heat-Shock Response , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Onions/cytology , Onions/metabolism , Peptide Fragments/chemistry , Peptide Fragments/genetics , Peptide Fragments/metabolism , Plant Epidermis/cytology , Plant Epidermis/metabolism , Plant Proteins/chemistry , Plant Proteins/genetics , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Transcription Factors/chemistry , Transcription Factors/genetics , Transcriptional Activation , Two-Hybrid System Techniques
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