Shaping of the chick neuroepithelium during primary and secondary neurulation: Role of cell elongation

1987 ◽  
Vol 218 (2) ◽  
pp. 182-195 ◽  
Author(s):  
Gary C. Schoenwolf ◽  
Monica L. Powers
2021 ◽  
Vol 12 ◽  
Author(s):  
Judith García-González ◽  
Kasper van Gelderen

Primary root growth is required by the plant to anchor in the soil and reach out for nutrients and water, while dealing with obstacles. Efficient root elongation and bending depends upon the coordinated action of environmental sensing, signal transduction, and growth responses. The actin cytoskeleton is a highly plastic network that constitutes a point of integration for environmental stimuli and hormonal pathways. In this review, we present a detailed compilation highlighting the importance of the actin cytoskeleton during primary root growth and we describe how actin-binding proteins, plant hormones, and actin-disrupting drugs affect root growth and root actin. We also discuss the feedback loop between actin and root responses to light and gravity. Actin affects cell division and elongation through the control of its own organization. We remark upon the importance of longitudinally oriented actin bundles as a hallmark of cell elongation as well as the role of the actin cytoskeleton in protein trafficking and vacuolar reshaping during this process. The actin network is shaped by a plethora of actin-binding proteins; however, there is still a large gap in connecting the molecular function of these proteins with their developmental effects. Here, we summarize their function and known effects on primary root growth with a focus on their high level of specialization. Light and gravity are key factors that help us understand root growth directionality. The response of the root to gravity relies on hormonal, particularly auxin, homeostasis, and the actin cytoskeleton. Actin is necessary for the perception of the gravity stimulus via the repositioning of sedimenting statoliths, but it is also involved in mediating the growth response via the trafficking of auxin transporters and cell elongation. Furthermore, auxin and auxin analogs can affect the composition of the actin network, indicating a potential feedback loop. Light, in its turn, affects actin organization and hence, root growth, although its precise role remains largely unknown. Recently, fundamental studies with the latest techniques have given us more in-depth knowledge of the role and organization of actin in the coordination of root growth; however, there remains a lot to discover, especially in how actin organization helps cell shaping, and therefore root growth.


2015 ◽  
Vol 92 (1) ◽  
Author(s):  
Bongki Kim ◽  
Jeremy Roy ◽  
Winnie W.C. Shum ◽  
Nicolas Da Silva ◽  
Sylvie Breton
Keyword(s):  

1968 ◽  
Vol 24 (9) ◽  
pp. 926-926 ◽  
Author(s):  
M. C. Risueno ◽  
G. Giménez-Martín ◽  
J. F. López-Sáez

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Elizaveta Krol ◽  
Lisa Stuckenschneider ◽  
Joana M. Kästle Silva ◽  
Peter L. Graumann ◽  
Anke Becker

AbstractIn Rhizobiales bacteria, such as Sinorhizobium meliloti, cell elongation takes place only at new cell poles, generated by cell division. Here, we show that the role of the FtsN-like protein RgsS in S. meliloti extends beyond cell division. RgsS contains a conserved SPOR domain known to bind amidase-processed peptidoglycan. This part of RgsS and peptidoglycan amidase AmiC are crucial for reliable selection of the new cell pole as cell elongation zone. Absence of these components increases mobility of RgsS molecules, as well as abnormal RgsS accumulation and positioning of the growth zone at the old cell pole in about one third of the cells. These cells with inverted growth polarity are able to complete the cell cycle but show partially impaired chromosome segregation. We propose that amidase-processed peptidoglycan provides a landmark for RgsS to generate cell polarity in unipolarly growing Rhizobiales.


2008 ◽  
Vol 86 ◽  
pp. 0-0
Author(s):  
J GRAW ◽  
O PUK ◽  
M HORSCH ◽  
J BECKERS

2021 ◽  
Author(s):  
Takahiro Numata ◽  
Kenji Sugita ◽  
Arifa Ahamed Rahman ◽  
Abidur Rahman

Meristem, which sustains a reservoir of niche cells at its apex, is the most functionally dynamic part in a plant body. The shaping of the meristem requires constant cell division and cell elongation, that are regulated by hormones and cell cytoskeletal components, actin. Although the roles of hormones in regulating meristem development have been extensively studied, the role of actin in this process is still elusive. Using the single and double mutants of the vegetative class actin, we demonstrate that ACT7 plays a primary role in regulating the root meristem development. In absence of ACT7, but not ACT8 and ACT2, cellular depolymerization of actin is observed. Consistently, act7 mutant shows reduced cell division, cell elongation and meristem length. Intracellular distribution and trafficking of auxin transport proteins in the actin mutants revealed that ACT7 specifically functions in root meristem to facilitate the trafficking of auxin efflux carriers PIN1 and PIN2, and consequently the transport of auxin. Compared with act7, act7act8 double mutant shows slightly enhanced phenotypic response and altered intracellular trafficking. The altered distribution of auxin in act7 and act7act8 affects the roots response to ethylene but not to cytokinin. Collectively, our results suggest that Arabidopsis root meristem development is primarily controlled through actin isovariant ACT7 mediated modulation of auxin-ethylene response.


2015 ◽  
Vol 197 (15) ◽  
pp. 2499-2507 ◽  
Author(s):  
Kristen E. Howery ◽  
Katy M. Clemmer ◽  
Emrah Şimşek ◽  
Minsu Kim ◽  
Philip N. Rather

ABSTRACTA key regulator of swarming inProteus mirabilisis the Rcs phosphorelay, which repressesflhDC, encoding the master flagellar regulator FlhD4C2. Mutants inrcsB, the response regulator in the Rcs phosphorelay, hyperswarm on solid agar and differentiate into swarmer cells in liquid, demonstrating that this system also influences the expression of genes central to differentiation. To gain a further understanding of RcsB-regulated genes involved in swarmer cell differentiation, transcriptome sequencing (RNA-Seq) was used to examine the RcsB regulon. Among the 133 genes identified,minCandminD, encoding cell division inhibitors, were identified as RcsB-activated genes. A third gene,minE, was shown to be part of an operon withminCD. To examineminCDEregulation, theminpromoter was identified by 5′ rapid amplification of cDNA ends (5′-RACE), and both transcriptionallacZfusions and quantitative real-time reverse transcriptase (qRT) PCR were used to confirm that theminCDEoperon was RcsB activated. Purified RcsB was capable of directly binding theminCpromoter region. To determine the role of RcsB-mediated activation ofminCDEin swarmer cell differentiation, a polarminCmutation was constructed. This mutant formed minicells during growth in liquid, produced shortened swarmer cells during differentiation, and exhibited decreased swarming motility.IMPORTANCEThis work describes the regulation and role of the MinCDE cell division system inP. mirabilisswarming and swarmer cell elongation. Prior to this study, the mechanisms that inhibit cell division and allow swarmer cell elongation were unknown. In addition, this work outlines for the first time the RcsB regulon inP. mirabilis. Taken together, the data presented in this study begin to address howP. mirabiliselongates upon contact with a solid surface.


2019 ◽  
Vol 10 ◽  
Author(s):  
Marie-Clémence Duchêne ◽  
Thomas Rolain ◽  
Adrien Knoops ◽  
Pascal Courtin ◽  
Marie-Pierre Chapot-Chartier ◽  
...  

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