Discriminative gene co-expression network analysis uncovers novel modules involved in the formation of phosphate deficiency-induced root hairs in Arabidopsis

Jorge E. Salazar-Henao; Wen-Dar Lin; Wolfgang Schmidt

doi:10.1038/srep26820

Overexpression of OsPIN2 Regulates Root Growth and Formation in Response to Phosphate Deficiency in Rice

International Journal of Molecular Sciences ◽

10.3390/ijms20205144 ◽

2019 ◽

Vol 20 (20) ◽

pp. 5144

Author(s):

Huwei Sun ◽

Xiaoli Guo ◽

Fugui Xu ◽

Daxia Wu ◽

Xuhong Zhang ◽

...

Keyword(s):

Root Growth ◽

Growth And Development ◽

Plant Root ◽

Lateral Roots ◽

Root Hairs ◽

Phosphate Deficiency ◽

P Deficiency ◽

Auxin Distribution ◽

Seminal Roots ◽

Underlying Mechanisms

The response of root architecture to phosphate (P) deficiency is critical in plant growth and development. Auxin is a key regulator of plant root growth in response to P deficiency, but the underlying mechanisms are unclear. In this study, phenotypic and genetic analyses were undertaken to explore the role of OsPIN2, an auxin efflux transporter, in regulating the growth and development of rice roots under normal nutrition condition (control) and low-phosphate condition (LP). Higher expression of OsPIN2 was observed in rice plants under LP compared to the control. Meanwhile, the auxin levels of roots were increased under LP relative to control condition in wild-type (WT) plants. Compared to WT plants, two overexpression (OE) lines had higher auxin levels in the roots under control and LP. LP led to increased seminal roots (SRs) length and the root hairs (RHs) density, but decreased lateral roots (LRs) density in WT plants. However, overexpression of OsPIN2 caused a loss of sensitivity in the root response to P deficiency. The OE lines had a shorter SR length, lower LR density, and greater RH density than WT plants under control. However, the LR and RH densities in the OE lines were similar to those in WT plants under LP. Compared to WT plants, overexpression of OsPIN2 had a shorter root length through decreased root cell elongation under control and LP. Surprisingly, overexpression of OsPIN2 might increase auxin distribution in epidermis of root, resulting in greater RH formation but less LR development in OE plants than in WT plants in the control condition but levels similar of these under LP. These results suggest that higher OsPIN2 expression regulates rice root growth and development maybe by changing auxin distribution in roots under LP condition.

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Use of SEM, X-ray analysis and TEM to localize Fe3+ reduction in roots

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100104029 ◽

1988 ◽

Vol 46 ◽

pp. 392-393 ◽

Cited By ~ 3

Author(s):

William P. Wergin ◽

P. F. Bell ◽

Rufus L. Chaney

Keyword(s):

Electron Microscopy ◽

Root Hairs ◽

Rapid Reduction ◽

X Ray ◽

Physical Evidence ◽

Transmission Electron ◽

Young Root ◽

Insoluble Precipitate ◽

Uptake And Transport ◽

Scanning Electron

In dicotyledons, Fe3+ must be reduced to Fe2+ before uptake and transport of this essential macronutrient can occur. Ambler et al demonstrated that reduction along the root could be observed by the formation of a stain, Prussian blue (PB), Fe4 [Fe(CN)6]3 n H2O (where n = 14-16). This stain, which is an insoluble precipitate, forms at the reduction site when the nutrient solution contains Fe3+ and ferricyanide. In 1972, Chaney et al proposed a model which suggested that the Fe3+ reduction site occurred outside the cell membrane; however, no physical evidence to support the model was presented at that time. A more recent study using the PB stain indicates that rapid reduction of Fe3+ occurs in a region of the root containing young root hairs. Furthermore the most pronounced activity occurs in plants that are deficient in Fe. To more precisely localize the site of Fe3+ reduction, scanning electron microscopy (SEM), x-ray analysis, and transmission electron microscopy (TEM) were utilized to examine the distribution of the PB precipitate that was induced to form in roots.

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Techniques for preparing the Lolium perenne coleorhiza for scanning electron microscope evaluation

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100124239 ◽

1992 ◽

Vol 50 (1) ◽

pp. 766-767

Author(s):

Susan B.G. Debaene ◽

John S. Gardner ◽

Phil S. Allen

Keyword(s):

Electron Microscope ◽

Scanning Electron Microscope ◽

Lolium Perenne ◽

Morphological Study ◽

Root Hairs ◽

Inner Pressure ◽

Water Potentials ◽

Radicle Emergence ◽

Standard Fixation ◽

Scanning Electron

The coleorhiza is a nonvascular sheath that encloses the embryonic radicle in Poaceae, and is generally the first tissue to emerge during germination. Delicate hairlike extensions develop from some coleorhiza cells prior to radicle emergence. Similar to root hairs, coleorhiza hairs are extremely sensitive to desiccation and are damaged by exposure to negative water potentials. The coleorhiza of Lolium perenne is somewhat spherical when first visible, after which a knob forms at a right angle to the caryopsis due to inner pressure from the elongating radicle. This knob increases in length until the radicle finally punctures the coleorhiza. Standard fixation procedures cause severe desiccation of coleorhiza cells and hairs, making morphological study of the coleorhiza difficult. This study was conducted to determine a more successful process for coleorhiza preservation.

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SEM and fluorescence imaging of callose deposition in root hair tips and suspension cultures of Streptanthus tortuosus

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100161047 ◽

1990 ◽

Vol 48 (3) ◽

pp. 698-699

Author(s):

K.S. Walters ◽

R.D. Sjolund ◽

K.C. Moore

Keyword(s):

Cell Wall ◽

Root Hair ◽

Cultured Cells ◽

Root Hairs ◽

Callus Cultures ◽

Callose Deposition ◽

Culture Cells ◽

Wall Structures ◽

Ultraviolet Illumination ◽

Callose Formation

Callose, B-1,3-glucan, a component of cell walls, is associated with phloem sieve plates, plasmodesmata, and other cell wall structures that are formed in response to wounding or infection. Callose reacts with aniline blue to form a fluorescent complex that can be recognized in the light microscope with ultraviolet illumination. We have identified callose in cell wall protuberances that are formed spontaneously in suspension-cultured cells of S. tortuosus and in the tips of root hairs formed in sterile callus cultures of S. tortuosus. Callose deposits in root hairs are restricted to root hair tips which appear to be damaged or deformed, while normal root hair tips lack callose deposits. The callose deposits found in suspension culture cells are restricted to regions where unusual outgrowths or protuberances are formed on the cell surfaces, specifically regions that are the sites of new cell wall formation.Callose formation has been shown to be regulated by intracellular calcium levels.

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