Faculty Opinions recommendation of PHABULOSA controls the quiescent center-independent root meristem activities in Arabidopsis thaliana.

Author(s):  
Vitaly Citovsky ◽  
Renhong Wu
PLoS Genetics ◽  
2015 ◽  
Vol 11 (3) ◽  
pp. e1004973 ◽  
Author(s):  
Jose Sebastian ◽  
Kook Hui Ryu ◽  
Jing Zhou ◽  
Danuše Tarkowská ◽  
Petr Tarkowski ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Mónica L. García-Gómez ◽  
Adriana Garay-Arroyo ◽  
Berenice García-Ponce ◽  
María de la Paz Sánchez ◽  
Elena R. Álvarez-Buylla

The root stem cell niche (SCN) of Arabidopsis thaliana consists of the quiescent center (QC) cells and the surrounding initial stem cells that produce progeny to replenish all the tissues of the root. The QC cells divide rather slowly relative to the initials, yet most root tissues can be formed from these cells, depending on the requirements of the plant. Hormones are fundamental cues that link such needs with the cell proliferation and differentiation dynamics at the root SCN. Nonetheless, the crosstalk between hormone signaling and the mechanisms that regulate developmental adjustments is still not fully understood. Developmental transcriptional regulatory networks modulate hormone biosynthesis, metabolism, and signaling, and conversely, hormonal responses can affect the expression of transcription factors involved in the spatiotemporal patterning at the root SCN. Hence, a complex genetic–hormonal regulatory network underlies root patterning, growth, and plasticity in response to changing environmental conditions. In this review, we summarize the scientific literature regarding the role of hormones in the regulation of QC cell proliferation and discuss how hormonal signaling pathways may be integrated with the gene regulatory network that underlies cell fate in the root SCN. The conceptual framework we present aims to contribute to the understanding of the mechanisms by which hormonal pathways act as integrators of environmental cues to impact on SCN activity.


2019 ◽  
Author(s):  
Sylvia Illgen ◽  
Stefanie Zintl ◽  
Ellen Zuther ◽  
Dirk K. Hincha ◽  
Thomas Schmülling

AbstractThe ETHYLENE RESPONSE FACTOR (ERF) genes of Arabidopsis thaliana form a large family encoding plant-specific transcription factors. Here, we characterise the four phylogenetically closely related ERF102/ERF5, ERF103/ERF6, ERF104 and ERF105 genes. Expression analyses revealed that these four genes are similarly regulated by different hormones and abiotic stresses. Analyses of tissue-specific expression using promoter:GUS reporter lines revealed their predominant expression in root tissues including the root meristem (ERF103), the quiescent center (ERF104) and the root vasculature (all). All GFP-ERF fusion proteins were nuclear-localised. The analysis of insertional mutants, amiRNA lines and 35S:ERF overexpressing transgenic lines indicated that ERF102 to ERF105 have only a limited impact on regulating shoot and root growth. Previous work had shown a role for ERF105 in the cold stress response. Here, measurement of electrolyte leakage to determine leaf freezing tolerance and expression analyses of cold-responsive genes revealed that the combined activity of ERF102 and ERF103 is also required for a full cold acclimation response likely involving the CBF regulon. Together, these results suggest a common function of these ERF genes in regulating root architecture and the response to cold stress.


1992 ◽  
Vol 101 (3) ◽  
pp. 483-493
Author(s):  
TSUNEYOSHI KUROIWA ◽  
MAKOTO FUJIE ◽  
HARUKO KUROIWA

The fate of mitochondrial nuclei (known as nucleoids or mt-nuclei), which contain extremely small amounts of DNA, was followed in thin sections of the root meristem of Pelargonium zonale by embedding of samples in Technovit 7100 resin and double staining with 4′-6-diamidino-2-phenylindole (DAPI) and acridine orange, in combination with light-microscopic autoradiography and microphotometry. The synthesis of cell-nuclear DNA and cell division occurs actively in the root meristem, between 150 μm and 700 μm from the tip of the root. For simplicity, cells in S phase in the cortex were selected for main analysis as the model system for examination of cell proliferation. It is estimated, on the basis of the length of the cells in longitudinal median sections, that the cells in the cortex, which are generated in the area just above the quiescent center (QC) about 150 μm from the tip, enter the elongation zone after at least five divisions. In the entire cortex, individual cells in S phase have approximately 230 mitochondria that each contain one mt-nucleus. The observation suggests that individual mitochondria divide once per mitotic cycle in the entire region of the meristem. By contrast, on the basis of incorporation of [3H]thymidine into mt-nuclei, the synthesis of mitochondrial DNA (mtDNA) occurs independently of the mitotic cycle in a restricted region just above the QC. Fluorimetry, using a video-intensified microscope photon-counting system (VIMPICS), revealed that the mtDNA content per mt-nucleus in the cells just above QC, where the synthesis of mtDNA is active, corresponds to approximately 3000 kilobase pairs (kbp) but, in the meristematic cells just below the elongation zone of the root it falls to less than 170 kbp. These findings strongly suggest that the amount of mtDNA per mitochondrion which has been synthesized in the region just above the QC is reduced stepwise as a result of continuous divisions of mitochondria in the absence of the synthesis of mtDNA. This phenomenon would explain why differentiated cells with a large vacuole in the elongation zone have mitochondria that contain only extremely small amounts of mtDNA.


Genetics ◽  
1997 ◽  
Vol 146 (1) ◽  
pp. 401-407
Author(s):  
Jean E Masson ◽  
Patrick J King ◽  
Jerzy Paszkowski

A simple screening method was developed for the isolation of Arabidopsis thaliana mutants hypersensitive to X-ray irradiation. The root meristem was used as the target for irradiation with sublethal doses of X rays, while protection of the shoot meristem by a lead cover allowed the rescue of hypersensitive individuals. We isolated nine independent X-ray-hypersensitive mutants from 7000 M2 seedlings. Analysis of three chosen mutants (xrs4, xrs9 and xrs11) showed that alterations in single recessive alleles are responsible for their phenotypes. The mutations are not allelic but linked and map to chromosome 4, suggesting mutations in novel genes as compared to previously mapped mutant alleles. Importantly, hypersensitivity to X rays was found to correlate with hypersensitivity to the DNA-alkylating agent mitomycin C, which provokes interstrand crosslinks, and/or to methyl methanesulfonate, which is known as a radiomimetic chemical. These novel phenotypes suggest that the mutants described here are altered in the repair of DNA damage, most probably by recombinational repair.


Plant Direct ◽  
2019 ◽  
Vol 3 (2) ◽  
pp. e00116 ◽  
Author(s):  
Mouli Ghosh Dastidar ◽  
Andrea Scarpa ◽  
Ira Mägele ◽  
Paola Ruiz-Duarte ◽  
Patrick von Born ◽  
...  

Science ◽  
2015 ◽  
Vol 347 (6222) ◽  
pp. 655-659 ◽  
Author(s):  
Brian C. W. Crawford ◽  
Jared Sewell ◽  
Greg Golembeski ◽  
Carmel Roshan ◽  
Jeff A. Long ◽  
...  

The root meristem consists of populations of distal and proximal stem cells and an organizing center known as the quiescent center. During embryogenesis, initiation of the root meristem occurs when an asymmetric cell division of the hypophysis forms the distal stem cells and quiescent center. We have identified NO TRANSMITTING TRACT (NTT) and two closely related paralogs as being required for the initiation of the root meristem. All three genes are expressed in the hypophysis, and their expression is dependent on the auxin-signaling pathway. Expression of these genes is necessary for distal stem cell fate within the root meristem, whereas misexpression is sufficient to transform other stem cell populations to a distal stem cell fate in both the embryo and mature roots.


2017 ◽  
Vol 121 ◽  
pp. 14-20 ◽  
Author(s):  
Fabrizio Araniti ◽  
Leonardo Bruno ◽  
Francesco Sunseri ◽  
Marianna Pacenza ◽  
Ivano Forgione ◽  
...  

2020 ◽  
Author(s):  
Pengcheng Li ◽  
Junjie Ma ◽  
Xueping Sun ◽  
Chuanzhi Zhao ◽  
Changle Ma ◽  
...  

ABSTRACTImpaired plastid translation affects various aspects of plant development, but the molecular mechanism remains elusive. Here, we described that the reduced function of plastid translation elongation factor EF-Tu encoded by RAB GTPASE HOMOLOG 8D (Rab8d) elicits defects in root development, including the reduced meristem size, programmed cell death (PCD) in the stem cell niche (SCN), and quiescent center (QC) division. We found that the ATAXIA-TELANGIECTASIA-MUTATED (ATM)-SUPPRESSOR OF GAMMA RESPONSE 1 module mediated overexpression of SIAMSE-RELATED 5 in the root meristem region is responsible for the reduced meristem size in the rab8d mutant through arresting the cell cycle. The QC activation in rab8d is dependent on ETHYLENE RESPONSE FACTOR 115, which expression is tightly associated with the PCD in SCN. We further found that Rab8d physically interacts with GENOME UNCOUPLED 1 (GUN1), and GUN1 is required for inducing PCD in the rab8d SCN. However, the loss of GUN1 function in rab8d severely impairs the root architecture, suggesting that the GUN1-mediated renewal of stem cells is essential for maintaining root growth. Our observations extend our knowledge on the roles of ATM and GUN1 in regulating root development through mediating plastid translation dependent signals.One-sentence summaryThe rab8d-dependent plastid signal mediated by ATM and GUN1 regulates the root meristem size and renewal of root stem cells, respectively.


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